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Suite ID Suite version Date of first commit of the suite Tool IDs Description EDAM topic(s) EDAM operation(s) Suite runs on main servers bio.tools (if available) Conda id biii Status Availability across Galaxies
0.0.1+galaxy0 source_extractor_astro_tool Tool to extract luminous sources from astronomical sky images 0
astropy
To update
UseGalaxy.eu1
0.0.1+galaxy0 sgwb_astro_tool SGWB 7
ipython
To update
UseGalaxy.eu1
0.0.1+galaxy0 plot_tools_astro_tool Plot Tools 0
pandas
To update
UseGalaxy.eu1
0.0.2+galaxy0 hess_astro_tool Basic analysis of Data Level 3 public data sample of HESS gamma-ray telescope 2
ipython
To update
UseGalaxy.eu1
0.0.1+galaxy0 grb_detection_astro_tool SPI-ACS GRB detection 0
numpy
To update
UseGalaxy.eu1
0.0.1+galaxy0 fits2tiff_astro_tool Tool to convert FITS files to TIFF 0
astropy
To update
UseGalaxy.eu1
0.0.2+galaxy0 desi_legacy_survey_astro_tool Tool to query Legacy Survey data 0
astropy
To update
UseGalaxy.eu1
0.0.1+galaxy0 cta_astro_tool Basic simulation of CTA telescope observations using gammapy package 1
unzip
To update
UseGalaxy.eu1
0.0.2+galaxy0 crbeam_astro_tool CRbeam 0
crbeam
To update
UseGalaxy.eu1
0.1.0+galaxy1 astropy_csv2fits astropy_fits2bitmap astropy_fits2csv astropy_fitsinfo AstropyTools library contains Galaxy tools for elementary Astrophysical operations 13
astropy
To update
UseGalaxy.cz3 UseGalaxy.eu4
0.10.21 astronomical_archives Astronomical archives tools contains tools for querying and fetching resources from astronomical archives into Galaxy 55
astropy
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.0.1+galaxy0 analyse_short_astro_text_astro_tool Tool to analyse short astrophysics texts 0
astroquery
To update
UseGalaxy.eu1
0.1.0+galaxy0 xlsx2tsv Convert an xlsx file to a tabular 0
pandas
To update
UseGalaxy.eu1
2.2.4 virsorter VirSorter2 applies a multi-classifier, expert-guided approach to detect diverse DNA and RNA virus genomes. Metagenomics Taxonomic classification 344
virsorter
Up-to-date
UseGalaxy.eu1 UseGalaxy.fr1
1.2.1 vibrant Virus Identification By iteRative ANnoTation Metagenomics Microbial ecology Sequence assembly Molecular interactions, pathways and networks Endocrinology and metabolism Sequence trimming Scaffolding Genome annotation 19
vibrant
Up-to-date
UseGalaxy.eu1 UseGalaxy.or1
3.0.1 dr_curve A tool for analyzing and visualizing the relationship between various doses and their corresponding biological responses 0
r-drc
To update
0.1.0+galaxy0 tt_baseline Toxicity prediction using QSAR models 0
pandas
To update
0.3 singularity_scriptrunner suite_scripting 0
To update
2.6.0 saqc saqc_executor System for automated Quality Control 0
saqc
To update
UseGalaxy.eu1
0.2.0 phi_toolkit_report Phage host interaction toolkit report generator 0
bioconductor-biostrings
To update
UseGalaxy.or1
2.1.11 phabox_cherry phabox_contamination phabox_end_to_end phabox_phagcn phabox_phamer phabox_phatyp phabox_phavip phabox_tree phabox_votu Identify and analyze phage contigs in metagenomic data Metagenomics Microbial ecology Sequence assembly Taxonomy Sequence assembly Taxonomic classification Visualisation 0
phabox
To update
5.18.0 omero_dataset_to_plate omero_filter omero_get_id omero_get_value omero_import omero_metadata_import omero_roi_import Interact with an OMERO.server using omero-py and ezomero. Imaging Data visualisation Image analysis 0
To update
UseGalaxy.eu3
0.4.0 msh2vtu shp2msh A suite of tools for OpenGeoSys (ogs) 0
ogstools
To update
6.5.3 ogs_addlayer ogs_extractboundary ogs_extractsurface ogs_generatestructuredmesh ogs_identifysubdomains ogs_simulation A suite of tools for OpenGeoSys (ogs) 0
To update
0.3.0 longORF obtain longest ORF in six-frame translations 0
To update
0.1.0+galaxy0 lm_get_projects Lambda-Miner Tools 0
pandas
To update
1.3.3 iphop_predict Integrated Phage Host Prediction Sample comparison 0
iphop
To update
UseGalaxy.eu1 UseGalaxy.or1
1.11.1 genomad_end_to_end Identify virus and plasmid genomes from nucleotide sequences Sequence analysis Sequence annotation Taxonomic classification 1658
genomad
Up-to-date
UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
2.1.3 eukcc_single Galaxy wrapper for EukCC Metagenomics Sequence assembly validation 0
eukcc
Up-to-date
2.1 dfpl_predict dfpl_train Galaxy wrapper for deepFPlearn. 0
deepfplearn
Up-to-date
1.3.6 dfast Prokaryotic genome annotation Nucleic acid structure analysis Genomics Sequence analysis Genome annotation 0
dfast
Up-to-date
1.0.3 checkv_end_to_end Assess quality of single-contig viral genomes Metagenomics Sequence assembly Metagenomic sequencing Mapping Sequence assembly Validation Read mapping 38
checkv
Up-to-date
UseGalaxy.eu1 UseGalaxy.or1
4.2.0 FROGS_affiliation_filters FROGS_affiliation_postprocess FROGS_affiliation_stats FROGS_biom_to_stdBiom FROGS_biom_to_tsv FROGS_cluster_filters FROGS_cluster_stats FROGS_clustering FROGS_demultiplex FROGSSTAT_DESeq2_Preprocess FROGSSTAT_DESeq2_Visualisation FROGSFUNC_step2_functions FROGSFUNC_step3_pathways FROGSFUNC_step1_placeseqs FROGS_itsx FROGS_normalisation FROGSSTAT_Phyloseq_Alpha_Diversity FROGSSTAT_Phyloseq_Beta_Diversity FROGSSTAT_Phyloseq_Sample_Clustering FROGSSTAT_Phyloseq_Composition_Visualisation FROGSSTAT_Phyloseq_Import_Data FROGSSTAT_Phyloseq_Multivariate_Analysis_Of_Variance FROGSSTAT_Phyloseq_Structure_Visualisation FROGS_preprocess FROGS_remove_chimera FROGS_taxonomic_affiliation FROGS_Tree FROGS_tsv_to_biom Suite for metabarcoding analysis 60685
frogs
To update
UseGalaxy.fr28
2.16.0 blastxml_to_tabular get_species_taxids ncbi_blastdbcmd_info ncbi_blastdbcmd_wrapper ncbi_blastn_wrapper ncbi_blastp_wrapper ncbi_blastx_wrapper ncbi_convert2blastmask_wrapper ncbi_deltablast_wrapper ncbi_dustmasker_wrapper ncbi_makeblastdb ncbi_makeprofiledb ncbi_psiblast_wrapper ncbi_rpsblast_wrapper ncbi_rpstblastn_wrapper ncbi_segmasker_wrapper ncbi_tblastn_wrapper ncbi_tblastx_wrapper NCBI BLAST+ 1560984
blast
To update
UseGalaxy.be16 UseGalaxy.cz16 UseGalaxy.eu16 UseGalaxy.fr16 UseGalaxy.no15 UseGalaxy.or16
0.0.3 make_nr Make a FASTA file non-redundant Molecular biology Sequence analysis Sequence alignment Genome annotation 0
biopython
To update
0.1.2 blastxml_to_top_descr Make table of top BLAST match descriptions Sequence analysis Sequence alignment Sequence annotation 265716
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.3.0 blast_reciprocal_best_hits BLAST Reciprocal Best Hits (RBH) from two FASTA files Nucleic acid sites, features and motifs Gene functional annotation Nucleic acid sequence analysis 27781
biopython
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.0.11 blast2go Maps BLAST results to GO annotation terms Nucleic acid sites, features and motifs Gene functional annotation 1248
b2g4pipe
To update
UseGalaxy.cz1 UseGalaxy.no1
0.0.5 uploadROIandMeasuresToOMERO Upload the ROI coordinates and the measurements to the omero server 0
omero-py
To update
0.0.2 revertR2orientationInBam Revert the mapped orientation of R2 mates in a bam. 578
samtools
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
20240214 omero_hyperstack_to_gastruloid_measurements Analyse Hyperstack on OMERO server to segment gastruloid and compute measurements 0
fiji
To update
20230809 omero_hyperstack_to_fluo_measurements_on_gastruloid Analyse Hyperstack on OMERO server to measure fluorescence levels 0
fiji
To update
20240521 omero_get_full_images Get full images from omero 0
fiji
To update
0.2.0 omero_get_children_ids Get omero id of children of an omero object id 0
omero-py
To update
20230623 omero_clean_rois_tables Remove all ROIs and all tables on OMERO associated to an omero object and recursively up and down 0
fiji
To update
20221216 measureGastruloids Get the ROI coordinates around the gastruloids as well as measurements like Area, elongation index 0
fiji
To update
20241213.2 max_projections_stack_and_upload_omero Combine images from max projections to stack and upload to the omero server 0
Fiji
To update
20231221 incucyte_stack_and_upload_omero Combine images to stack and upload to the omero server 0
Fiji
To update
20241220 hyperstack_to_bleach_corrected_movie Generate blach corrected movie from hyperstack 0
Fiji
To update
0.0.2 getTn5ExtendedCoverage Take an input bam from ATAC-seq and generate a bedgraph using the center of the Tn5 insertion with an extension 0
pysam
To update
0.11.1+galaxy1 fromgtfTobed12 Convert GTF files to BED12 format 0
gffutils
To update
0.0.2 fromHicupToJuicebox Convert the output of hicup (as sam or bam) to the input of juicebox. 0
pysam
To update
0.9.3 cooler_balance cooler_cload_tabix cooler_csort_tabix cooler_makebins cooler_zoomify cooler different tools to process Hi-C from mirnylab 534
htslib
To update
UseGalaxy.cz4 UseGalaxy.eu5 UseGalaxy.or4
SNVPhyl suite defining all dependencies for SNVPhyl 0
To update
1.8.2 verify_map Checks the mapping quality of all BAM(s) 0
snvphyl-tools
Up-to-date
1.8.2 vcf2snvalignment Generates multiple alignment of variant calls 0
snvphyl-tools
Up-to-date
1.8.2 snvmatrix Generate matrix of SNV distances 0
snvphyl-tools
Up-to-date
1.8.2 positions2snv_invariant_alignment Generate alignment of SNVs and non-variant positions from SNVPhyl variant table. 0
snvphyl-tools
Up-to-date
1.8.2 positions2snv_alignment Generate alignment of SNVs from SNVPhyl variant table. 0
snvphyl-tools
Up-to-date
1.8.2 findrepeat Find repetitive regions on a reference genome using MUMMer 0
snvphyl-tools
Up-to-date
1.8.2 filtervcf SNVPhyl filter_vcf 0
snvphyl-tools
Up-to-date
1.8.2 filterstat SNVPhyl filter_stats 0
snvphyl-tools
Up-to-date
1.8.2 filterdensity Filter out position based on distance between SNVs 0
snvphyl-tools
Up-to-date
1.8.2 consolidate_vcfs Combines freebayes and mpileup files for use by vcf2snvalignment 0
snvphyl-tools
Up-to-date
6.6.1 xtb_molecular_optimization Performs semiempirical molecular optimization. 262
xtb
To update
UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
wtv
0.1.0 wtv A cli/python library for ion selection in mass spectrometry. Metabolomics Feature selection 0
wtv
wtv
Up-to-date
0.2.0 waveica Removal of batch effects for large-scale untargeted metabolomics data based on wavelet analysis. Metabolomics Standardisation and normalisation 298
r-recetox-waveica
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
table_pandas_arithmetics table_pandas_rename_column table_pandas_rename_columns_regex table_pandas_transform table_scipy_interpolate Tools to manipulate and analyze data tables. 0
scipy
To update
UseGalaxy.eu5
0.8.0 spec2vec_similarity spec2vec_training Mass spectra similarity scoring using a trained Spec2Vec model. Proteomics experiment Metabolomics Natural language processing Proteomics Spectrum calculation Spectral library search Database search Natural product identification 115
spec2vec
Up-to-date
UseGalaxy.eu2 UseGalaxy.or2
3.0.0 rmassbank RMassBank is an R package for processing tandem MS files and building of MassBank records. 68
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
0.4.1 riassigner riassigner_from_comment Metabolomics Compound libraries and screening Data submission, annotation and curation Standardisation and normalisation 302
riassigner
To update
UseGalaxy.cz1 UseGalaxy.eu2 UseGalaxy.fr1 UseGalaxy.or2
0.5.4 retip_apply retip_descriptors retip_filter_rt retip_train Metabolomics Proteomics experiment Machine learning Cheminformatics Chemistry Retention time prediction Spectrum calculation Deisotoping Formatting Deposition 0
To update
1.0.0 rename_annotated_feature Update column names in an abundance table using a annotation table with spectral matching results 40
pandas
To update
UseGalaxy.eu1 UseGalaxy.or1
1.0.0 rem_complex Removes molecular coordination complexes. 99
pandas
To update
UseGalaxy.eu1 UseGalaxy.or1
0.10.0 recetox_xmsannotator_advanced Expression profile pathway mapping Structure comparison Isotopic distributions calculation Annotation 133
r-recetox-xmsannotator
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
v3.5.2 recetox_msfinder Metabolomics Annotation 146
To update
UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
3.5.1 rcx_boxplot recetox-boxplot is a tool for plotting boxplots from a tabular/csv/parquet data file. 0
r-ggplot2
To update
0.13.4 recetox_aplcms_align_features recetox_aplcms_compute_clusters recetox_aplcms_compute_template recetox_aplcms_correct_time recetox_aplcms_generate_feature_table recetox_aplcms_merge_known_table recetox_aplcms_recover_weaker_signals recetox_aplcms_remove_noise Peak detection tool for HRMS profile data. Metabolomics Chromatographic alignment Quantification Peak detection Feature extraction Alignment 2638
r-recetox-aplcms
To update
UseGalaxy.cz8 UseGalaxy.eu8 UseGalaxy.fr8 UseGalaxy.or8
0.1.0 rcx-tk Tools to process metadata or alkane files. 0
rcx-tk
Up-to-date
UseGalaxy.eu1
1.3.1 ramclustr ramclustr_define_experiment Metabolomics Imputation Standardisation and normalisation Clustering Correlation 859
r-ramclustr
Up-to-date
UseGalaxy.cz2 UseGalaxy.eu2 UseGalaxy.fr2 UseGalaxy.or2
0.2 query Execute an SQL statement on a set of tables 0
click
To update
5.2.1 qcxms_getres qcxms_neutral_run qcxms_production_run QCxMS is a quantum chemical (QC) based program that enables users to calculate mass spectra (MS) using Born-Oppenheimer Molecular Dynamics (MD). 36360
To update
UseGalaxy.eu3 UseGalaxy.or3
1.0.6 mztabm_validate Tools for handling mzTab-M files using various packages. Ontology and terminology Metabolomics Data submission, annotation and curation Loading Format validation Formatting 0
jmztab-m
Up-to-date
1.0.7 mzspeclib_convert mzspeclib_describe mzspeclib_validate mzspeclib is a library and set of tools for handling, converting, and validating mass spectral libraries in a standardized format. This suite provides Galaxy wrappers for mzspeclib's core functionalities, including conversion and validation of spectral libraries. Proteomics Metabolomics Conversion Format validation 0
mzspeclib
Up-to-date
0.1.0+galaxy2 mzml_validator mzML Validator checks if mzML file validates against XML Schema Definition of HUPO Proteomics Standard Initiative. 0
lxml
To update
0.1.0 msp_merge 0
matchms
To update
0.4.1 msmetaenhancer Metabolomics Compound libraries and screening Data submission, annotation and curation Annotation Standardisation and normalisation 287
msmetaenhancer
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
2.0.0 ms2deepscore_config_generator ms2deepscore_similarity ms2deepscore_training Mass spectra similarity scoring using a trained ms2deepscore model. Proteomics experiment Machine learning Metabolomics Small molecules Compound libraries and screening Spectrum calculation Spectral library search Network analysis 0
ms2deepscore
To update
UseGalaxy.eu3
1.0.0 target_screen use_theoretical_mz_annotations 186
pandas
To update
UseGalaxy.eu2 UseGalaxy.or1
1.1.2 mfassignr_findRecalSeries mfassignr_histnoise mfassignr_isofiltr mfassignr_kmdnoise mfassignr_mfassign mfassignr_mfassignCHO mfassignr_recal mfassignr_recallist mfassignr_snplot The MFAssignR package was designed for multi-element molecular formula (MF) assignment of ultrahigh resolution mass spectrometry measurements Proteomics experiment Molecular interactions, pathways and networks Workflows Visualisation 50
r-mfassignr
Up-to-date
UseGalaxy.eu9 UseGalaxy.or9
0.30.2 matchms_add_key matchms_convert matchms_matchms_export_skyline_transition_list matchms_filtering matchms_fingerprint_similarity matchms_formatter matchms_metadata_export matchms_metadata_match matchms_metadata_merge matchms_networking matchms_remove_key matchms_remove_spectra matchms_spectral_similarity matchms_split matchms_subsetting Searching, filtering and converting mass spectral libraries. Metabolomics Spectral library search Format validation Filtering 4786
matchms
Up-to-date
UseGalaxy.cz9 UseGalaxy.eu14 UseGalaxy.fr11 UseGalaxy.or14
2.6+galaxy3 isolib Create an isotopic pattern library for given compounds and adducts. 63
bioconductor-metabocoreutils
To update
UseGalaxy.eu1 UseGalaxy.or1
1.3.0 ipapy2_MS1_annotation ipapy2_MS2_annotation ipapy2_clustering ipapy2_compute_all_adducts ipapy2_compute_bio ipapy2_gibbs_sampler ipapy2_gibbs_sampler_add ipapy2_map_isotope_patterns Mass spectrometry data annotation tool. 0
ipapy2
Up-to-date
1.0.1 gc_derivatization In silico derivatization for GC. 22
gc-meox-tms
Up-to-date
UseGalaxy.eu1 UseGalaxy.or1
1.0.0+galaxy0 freqsap Get frequencies of single amino-acid polymorphisms based on nucleid-acid polymorphism for different populations from UniProt and DbSNP. 0
pandas
To update
3.1.1 filter_orgmet_anorg Tool for filtering organometallics/anorganic compounds from a list of compounds. 0
openbabel
To update
3.0.20230403 biotransformer BioTransformer is a tool for prediction of small molecule metabolism in mammals. Small molecules Endocrinology and metabolism Metabolomics Carbohydrates NMR Metabolic pathway prediction PTM site prediction Natural product identification 67
biotransformer
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
1.16.0 bioconductor_scp scp is a package for the single cell proteomics data processing. Proteomics experiment Proteomics Visualisation Expression analysis 0
scp
bioconductor-scp
Up-to-date
UseGalaxy.eu1 UseGalaxy.or1
2.40.0 bioconductor_mzr_convert Galaxy wrapper for the Bioconductor mzR package, enabling conversion between common mass spectrometry data formats (mzML, mzXML, netCDF) within Galaxy workflows. Proteomics Proteomics experiment Data management Formatting 0
mzr
bioconductor-mzr
Up-to-date
2.32.0 bioconductor_msnbase_centroid bioconductor_msnbase_smooth_chromatogram bioconductor_msnbase_smooth_mz MSnbase provides infrastructure for manipulation, processing and visualisation of mass spectrometry and proteomics data, ranging from raw to quantitative and annotated data. Proteomics Proteomics experiment Data management Data visualisation Data handling Visualisation 0
bioconductor-msnbase
Up-to-date
UseGalaxy.eu3
1.0.0+galaxy1 ucsc_cell_browser Python pipeline and Javascript scatter plot library for single-cell datasets 982
ucsc-cell-browser
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
4.0.0 seurat_convert seurat_dim_plot seurat_export_cellbrowser seurat_filter_cells seurat_find_clusters seurat_find_markers seurat_find_neighbours seurat_find_variable_genes seurat_hover_locator seurat_integration seurat_map_query seurat_normalise_data seurat_plot seurat_read10x seurat_run_pca seurat_run_tsne seurat_run_umap seurat_scale_data seurat_select_integration_features De-composed Seurat functionality tools, based on https://github.com/ebi-gene-expression-group/r-seurat-scripts and Seurat 2.3.1 5795
seurat-scripts
To update
UseGalaxy.eu14 UseGalaxy.fr11 UseGalaxy.or14
1.0.2 scpred_get_feature_space scpred_get_std_output scpred_predict_labels scpred_train_model De-composed scPred functionality tools, see https://github.com/ebi-gene-expression-group/scpred-cli and r-scPred 1.0 25
scpred-cli
To update
UseGalaxy.eu4
1.6.4 scmap_get_std_output scmap_index_cell scmap_index_cluster scmap_preprocess_sce scmap_scmap_cell scmap_scmap_cluster scmap_select_features De-composed scmap functionality tools, based on https://github.com/ebi-gene-expression-group/scmap-cli and scmap 1.6.0. 114
scmap-cli
To update
UseGalaxy.cz1 UseGalaxy.eu7
0.0.5 sceasy_convert Convert scRNA data object between popular formats 1998
r-sceasy
To update
UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
0.0.9 run_sccaf sccaf_asses sccaf_asses_merger sccaf_regress_out SCCAF: Single Cell Clustering Assessment Framework. 111
sccaf
To update
UseGalaxy.eu4 UseGalaxy.or3
1.10.0 scater_calculate_cpm scater_calculate_qc_metrics scater_filter scater_is_outlier scater_normalize scater_read_10x_results De-composed Scater functionality tools, based on https://github.com/ebi-gene-expression-group/bioconductor-scater-scripts and Scater 1.8.4. 757
scater-scripts
To update
UseGalaxy.be2 UseGalaxy.cz2 UseGalaxy.eu6 UseGalaxy.no2 UseGalaxy.or2
1.9.3 anndata_ops scanpy_filter_cells scanpy_filter_genes scanpy_find_cluster scanpy_find_markers scanpy_find_variable_genes scanpy_integrate_bbknn scanpy_integrate_combat scanpy_integrate_harmony scanpy_integrate_mnn scanpy_plot_scrublet scanpy_multiplet_scrublet scanpy_compute_graph scanpy_normalise_data scanpy_parameter_iterator scanpy_plot_embed scanpy_plot_trajectory scanpy_read_10x scanpy_regress_variable scanpy_run_diffmap scanpy_run_dpt scanpy_run_fdg scanpy_run_paga scanpy_run_pca scanpy_run_tsne scanpy_run_umap scanpy_scale_data scanpy-scripts, command-line wrapper scripts around Scanpy. 63989
scanpy-scripts
To update
UseGalaxy.be1 UseGalaxy.cz14 UseGalaxy.eu27 UseGalaxy.no13 UseGalaxy.or27
1.8.0 sc3_calc_biology sc3_calc_consens sc3_calc_dists sc3_calc_transfs sc3_estimate_k sc3_kmeans sc3_prepare De-composed SC3 functionality tools, based on https://github.com/ebi-gene-expression-group/bioconductor-sc3-scripts and SC3 1.8.0. 13
sc3-scripts
To update
UseGalaxy.eu7
0.12.1 pyscenic_aucell pyscenic_binarize pyscenic_ctx pyscenic_grn PySCENIC scripts based on usage at https://pyscenic.readthedocs.io/ 0
To update
0.1.4 monocle3_create monocle3_diffExp monocle3_learnGraph monocle3_orderCells monocle3_partition monocle3_plotCells monocle3_preprocess monocle3_reduceDim monocle3_topmarkers De-composed monocle3 functionality tools, based on https://github.com/ebi-gene-expression-group/monocle-scripts and monocle3 0.1.2. 5481
monocle3-cli
To update
UseGalaxy.eu9 UseGalaxy.or9
0.2.8 garnett_check_markers garnett_classify_cells garnett_get_feature_genes garnett_get_std_output garnett_train_classifier garnett_transform_markers update_marker_file De-composed Garnett functionality tools, see https://github.com/ebi-gene-expression-group/garnett-cli and r-garnett 0.2.8 27
garnett-cli
To update
UseGalaxy.eu7
1.0.4 dropletutils_empty_drops dropletutils_read_10x De-composed DropletUtils functionality tools, based on https://github.com/ebi-gene-expression-group/dropletutils-scripts and DropletUtils 1.0.3 2813
dropletutils-scripts
To update
UseGalaxy.cz2 UseGalaxy.eu2 UseGalaxy.fr2 UseGalaxy.or2
1.4.0+galaxy3 score_genes_aucell decoupler_pathway_inference decoupler_pseudobulk decoupler - Ensemble of methods to infer biological activities 122
decoupler
To update
UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
v0.0.2+galaxy2 retrieve_scxa Tools for interacting with the EMBL-EBI Expression Atlas resource https://www.ebi.ac.uk/gxa/home https://www.ebi.ac.uk/gxa/sc/home 1738
wget
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
v0.0.4+galaxy0 hca_matrix_downloader Tools for interacting with the Human Cell Atlas resource https://prod.data.humancellatlas.org/explore/projects 559
hca-matrix-downloader
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.6.3+galaxy1 celltypist_predict celltypist - Automated cell type annotation 0
celltypist
To update
1.1.1 ct_build_cell_ontology_dict ct_check_labels ct_combine_tool_outputs ct_downsample_cells ct_get_consensus_outputs ct_get_empirical_dist ct_get_tool_perf_table ct_get_tool_pvals Tools for analysis of predictions from scRNAseq cell type classification tools, see https://github.com/ebi-gene-expression-group/cell-types-analysis 9
cell-types-analysis
To update
UseGalaxy.eu6
0.0.1+galaxy6 _salmon_kallisto_mtx_to_10x Transforms .mtx matrix and associated labels into a format compatible with tools expecting old-style 10X data 1139
scipy
To update
UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
0.25.1+galaxy0 fastq_filter_n fastq_trim_poly_at Set of tools for handling fastq files 0
fastq_utils
To update
0.0.14+galaxy0 cshl_fastq_quality_trimmer FASTQ trimmer based on quality 0
fastx_toolkit
To update
1.0+galaxy0 fastq_pair Paired-end fastq pairer 0
fastq-pair
To update
1.52.0+galaxy0 _ensembl_gtf2gene_list Utility to extract annotations from Ensembl GTF files. 3734
atlas-gene-annotation-manipulation
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.4.4 fastq_provider Retrieval and download of FASTQ files from ENA and other repositories such as HCA. 0
atlas-fastq-provider
To update
1.6.1+galaxy2 _dropletBarcodePlot Make a cell barcode plot for droplet single-cell RNA-seq QC 1752
scxa-plots
To update
UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
0.1.0 smithsonian_volcanoes Retrieve data from Volcanoes of the World (VOTW) Database 0
python
To update
0.1.0 shyft_longitudes Shift longitudes ranging from 0. and 360 degrees to -180. and 180. degrees 80
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.3.1 psy_maps Visualization of regular geographical data on a map with psyplot 557
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.2.0 mean_per_zone Creates a png image showing statistic over areas as defined in the vector file 25
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
2.0 ctsm_fates EMERALD version of the Functionally Assembled Terrestrial Ecosystem Simulator (FATES) with Community Terrestrial Systems Model as host model 426
fates-emerald
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
0.2.0 cds_essential_variability Get Copernicus Essential Climate Variables for assessing climate variability 336
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.0.2 eodie Earth Observation Data Information Extractor 45
eodie
To update
UseGalaxy.cz1 UseGalaxy.eu1
1.0.2 climate_stripes Create climate stripes from a tabular input file 482
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
2.1.3 cesm Community Earth System Model (CESM) 14
cesm
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
cdo
2.0.0 cdo_info cdo_operations CDO (Climate Data Operators) is a collection of command line Operators to manipulate and analyse Climate and NWP model Data.Supported data formats are GRIB 1/2, netCDF 3/4, SERVICE, EXTRA and IEG. There are more than 600 operators available. 228
To update
UseGalaxy.cz2 UseGalaxy.eu2
0.1.0 cads Copernicus Atmosphere Data Store (ADS) 52
python
To update
UseGalaxy.cz1 UseGalaxy.eu1
c3s
0.3.0 c3s Copernicus Climate Change Service (C3S) 459
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
0.1.0 zoo_project_ogc_api_processes This tool is a wrapper for OGC API Processes (OTB) coming from the Zoo Project (https://zoo-project.github.io/docs/intro.html) and was created using the OGC-API-Process2Galaxy tool (https://github.com/AquaINFRA/OGC-API-Process2Galaxy). Check the README in the repository for more information. 26
r-base
To update
UseGalaxy.eu1
1.6.1 xmlstarlet Tool to convert a xml file from one metadata standard to another 103
xmlstarlet
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1
0.1.0 xarray_import_data A data import tool for opening OPeNDAP datasets and storing as netCDF files. 0
xarray
To update
UseGalaxy.eu1
0.1.1 vigiechiro_bilanenrichipf vigiechiro_bilanenrichirp vigiechiro_idcorrect_2ndlayer vigiechiro_idvalid Tools created by the vigiechiro team to analyses and identify chiro sounds files. 15636
To update
UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.fr4 UseGalaxy.no4
0.1.0 terrabyte_ogc_api_processes This tool is a wrapper for OGC API Processes (OTB) coming from terrabyte (https://docs.terrabyte.lrz.de/). 10
r-base
To update
UseGalaxy.eu1
0.0.2 stoceps_filteringsp stoceps_glm stoceps_glm_group stoceps_maketablecarrer stoceps_trend_indic Tools to analyse STOC data. 338
To update
UseGalaxy.cz5 UseGalaxy.eu5 UseGalaxy.fr5 UseGalaxy.no5
0.0.1 srs_diversity_maps srs_global_indices srs_process_data srs_spectral_indices srs_pca srs_preprocess_s2 srs_metadata Compute biodiversity indicators for remote sensing data from Sentinel 2 315
r-base
To update
UseGalaxy.cz7 UseGalaxy.eu7 UseGalaxy.fr7 UseGalaxy.or4
1.2.2 spocc_occ Get species occurences data 915
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1
0.2.15 sdmpredictors_list_layers Terrestrial and marine predictors for species distribution modelling. 3
r-base
To update
UseGalaxy.eu1
1.3.0 retrieve_bold Search a list of sequences in BOLD (Barcode of Life Data System) from specified taxa list and markers 10
r-base
To update
UseGalaxy.eu1
1.5 regionalgam_ab_index regionalgam_autocor_acf regionalgam_flight_curve regionalgam_glmmpql regionalgam_gls_adjusted regionalgam_gls regionalgam_plot_trend 546
r-mgcv
To update
UseGalaxy.be6 UseGalaxy.cz7 UseGalaxy.eu7 UseGalaxy.fr7 UseGalaxy.no7
1.0 otb_mean_shift_smoothing This application smooths an image using the MeanShift algorithm. 57
r-base
To update
UseGalaxy.eu1
1.0 otb_band_math Outputs a monoband image which is the result of a mathematical operation on several multi-band images. 99
r-base
To update
UseGalaxy.eu1
0.9.3 bgc_canyon_b Robust Estimation of Open Ocean CO2 Variables and Nutrient Concentrations From T, S, and O2 Data Using Bayesian Neural Networks 0
r-base
To update
UseGalaxy.eu1
2.1 tool_biogeochemical_calibration tool_odv tool_odv_history The tool merges various datasets with a common vocabulary and creates a single generic ODV spreadsheet in an automatic way. 0
To update
UseGalaxy.eu3
0.1.15 argo_getdata copernicusmarine divand_full_analysis Access, process, and visualise oceanographic data for the Earth System 99
copernicusmarine
To update
UseGalaxy.eu3
0.0.2 obisindicators obis_data Compute biodiveristy indicators for marine data from obis 374
r-base
To update
UseGalaxy.cz1 UseGalaxy.eu2 UseGalaxy.fr1 UseGalaxy.or1
0.1.0 iabiodiv_smartbiodiv_med_environ Retrieve environmental data from etopo, cmems and woa 34
pandas
To update
UseGalaxy.eu1
0.9.3.5 sanntis_marine The Sanntis tool identify biosynthetic gene clusters (BGCs) in genomic & metagenomic data 109
sanntis
To update
UseGalaxy.eu1 UseGalaxy.or1
0.1.0+galaxy0 data_paper_from_EML This tool derived from the R Shiny App MetaShRIMPS <https://github.com/TanguyGen/metaCure> is made to produce draft of data paper from Ecological Metadata Language (EML) based metadata documents. 24
r-base
To update
UseGalaxy.eu1
1.0 interpolation_run_idw_interpolation Run IDW interpolation based on a .csv and .geojson file 70
r-getopt
To update
UseGalaxy.eu1
0.2.0 hirondelle_crim This tool is a wrapper for OGC API Processes coming from https://osf.io/gfbws/. 236
r-base
To update
UseGalaxy.eu1
3.0.0 gdal_gdal_merge gdal_gdal_translate gdal_gdaladdo gdal_gdalbuildvrt gdal_gdalinfo gdal_gdalwarp gdal_ogr2ogr gdal_ogrinfo Geospatial Data Abstraction Library tools are all dedicated to manipulate raster and vector geospatial data formats. 1511
To update
UseGalaxy.cz8 UseGalaxy.eu8 UseGalaxy.fr8 UseGalaxy.no8
0.1.0 landcover_subindicator Access, process, visualise oceanographic data for the Earth System 2
numpy
To update
UseGalaxy.eu1
2022.3.0 timeseries_extraction xarray_coords_info xarray_mapplot xarray_metadata_info xarray_netcdf2netcdf xarray_select xarray (formerly xray) is an open source project and Python package that makes working withlabelled multi-dimensional arrays simple, efficient, and fun!xarray integrates with Dask to support parallel computations and streaming computation on datasetsthat don’t fit into memory. 6481
xarray
To update
UseGalaxy.cz6 UseGalaxy.eu6 UseGalaxy.fr5 UseGalaxy.no2 UseGalaxy.or2
0.0.0 tool_anonymization ecology_homogeneity_normality ecology_beta_diversity ecology_link_between_var ecology_presence_abs_abund ecology_stat_presence_abs Explore data through multiple statistical tools 1252
r-tangles
To update
UseGalaxy.cz6 UseGalaxy.eu6 UseGalaxy.fr6
1.0.0 aligned_to_consensus Tool to compute a consensus sequence from several aligned fasta sequences 5860
r-bioseq
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1
0.0.0 cb_dissim cb_ivr cb_div Compute indicators for turnover boulders fields 216
r-base
To update
UseGalaxy.cz3 UseGalaxy.eu3 UseGalaxy.fr3
3.0 harmonize_insitu_to_netcdf Process in-situ and biogechemical oceanographic Argo or Glider data for the Earth System 19
To update
UseGalaxy.eu1
0.7.0 aquainfra_ogc_api_processes Wrapper for OGC API Processes developed in the AquaINFRA project. 257
r-base
To update
UseGalaxy.eu1
1.0 aquainfra_importer A data source tool for downloading datasets via the AquaINFRA Interaction Platform. 277
To update
UseGalaxy.eu1
1.20.0 ab1_fastq_converter Tool to convert ab1 files into FASTQ files 62357
bioconductor-sangerseqr
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1
0.1.2 WormsMeasurements This tool uses WoRMS (World Register of Marine Species) to add measurement values to a dataset based on scientific names. 0
r-base
To update
UseGalaxy.eu1
1.0 phylo_index Tools to computes the phylodiversity index. 0
r-phyloregion
To update
UseGalaxy.eu1
1.0 phylogenetic_occupancy_matcher Tools to matches phylogenetic data with occupancy data. 0
r-phyloregion
To update
UseGalaxy.eu1
0.0.2 pampa_communitymetrics pampa_presabs pampa_glmcomm pampa_glmsp pampa_plotglm Tools to compute and analyse biodiversity metrics 2214
To update
UseGalaxy.cz5 UseGalaxy.eu5 UseGalaxy.fr5 UseGalaxy.no4 UseGalaxy.or5
0.1.0+galaxy0 Map_shp Mean_geom bar_plot Tools to compute The evolution of the total volume of very large trees, standing dead wood and dead wood on the ground on an area and the rate of devolution of the volume of wood favorable to biodiversity by large ecological regions (France). 89
r-base
To update
UseGalaxy.eu3 UseGalaxy.fr3
0.1.1+galaxy0 estimate_endem Tools to estimates the endemism of each cell in a spatial grid. 0
r-phyloregion
To update
UseGalaxy.eu1
0.1.2+galaxy0 ecoregion_brt_analysis ecoregion_GeoNearestNeighbor ecoregion_cluster_estimate ClaraGuess ecoregion_clara_cluster ecoregion_eco_map indicspecies ecoregion_taxa_seeker Tools to compute ecoregionalization with BRT model predictions and clustering. 642
r-base
To update
UseGalaxy.cz5 UseGalaxy.eu8 UseGalaxy.fr5
0.1.0+galaxy0 annotations_template eal_table_template eal_templates eml2eal eml_validate entities_template geo_cov_template makeeml raster_template taxo_cov_template vector_template Tools using EML Assembly Line R package to generate EML metadata from template metadata files and vice versa 618
r-base
To update
UseGalaxy.cz2 UseGalaxy.eu11 UseGalaxy.fr9
1.1 crsconverter Tools to transforms geographical vector data to a specified coordinate reference system. 0
r-sf
To update
UseGalaxy.eu1
2.5.1 yac Clips 3' adapters for small RNA sequencing reads. 0
python
To update
2.1+galaxy0 xpore_dataprep xpore_diffmod Identification and quantification of differential RNA modifications from direct RNA sequencing 0
xpore
To update
1.2.9 wisecondorx_npz_converter wisecondorx_predict wisecondorx_reference_builder WisecondorX 0
wisecondorx
Up-to-date
0.1 varscan_vaf Compute variant allele frequency in vcf files generated by varscan. 0
python
To update
0.6.1 tarfast5 produces a tar.gz archive of fast5 sequence files 0
pigz
To update
UseGalaxy.no1
2.8 sr_bowtie_dataset_annotation Maps iteratively small RNA sequencing datasets to reference sequences. 0
bowtie
To update
2.3.1 bowtieForSmallRNA bowtie wrapper tool to align small RNA sequencing reads Microbiology Biology 98
bowtie
To update
3.0.0+galaxy1 sequenzaindex snvtocnv infer copy number variations from a vcf file with SNVs using R sequenza 0
sequenza-utils
To update
3.4.2 overlapping_reads signature Computes the tendency of small RNAs to overlap with each other. 0
pysam
To update
3.1.1 small_rna_maps Generates small read maps from alignment BAM files 0
numpy
To update
1.3.0 small_rna_clusters clusters small rna reads in alignment BAM files 0
pysam
To update
2.2.0 sequence_format_converter various fasta to tabular conversions 0
python
To update
0.1.1 sashimi_plot Generates a sashimi plot from bam files. 0
python
To update
0.7.1+galaxy1 sambamba_sample_or_filter filter BAM/SAM on flags, fields, tags, and region, or down-sample, or slice BAM/SAM 836
sambamba
To update
UseGalaxy.or1
extract_transcript_to_gene_map_from_trinity purgegtffrommultichromgenes rsembowtie2 rsembowtie transcript quantification from RNA-Seq data 606
rsem
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
2.31.1 edger-repenrich2 repenrich2 Repeat element profiling using bowtie2 aligner 0
To update
2.31.1 edger-repenrich repenrich Repeat element profiling 1935
To update
UseGalaxy.or2
0.22.0 probecoverage computes and plots read coverage of genomic regions by sequencing datasets 0
pysam
To update
0.2.5b9 pindel Pindel detects genome-wide structural variation. 0
pindel
Up-to-date
1.40.0 pathifier pathifier 257
bioconductor-pathifier
To update
UseGalaxy.cz1 UseGalaxy.eu1
1.4.0 oasesoptimiserv Short read assembler 0
oases
To update
3.12.0 mutational_patterns Mutational patterns and signatures in base substitution catalogs 0
bioconductor-mutationalpatterns
To update
1.6 mircounts Generates miRNA count lists from read alignments to mirBase. 1646
tar
To update
UseGalaxy.or1
0.22.0 mapqstatistics Collects and shows the distribution of MAPQ values in a BAM alignment file 0
r-optparse
To update
1.6 manta Structural variant and indel caller for mapped sequencing data 568
manta
To update
UseGalaxy.cz1 UseGalaxy.eu1
1.3 lumpy Find structural variations 0
lumpy-sv
To update
0.2.8+galaxy1 lumpy_smoove vcf2hrdetect Galaxy wrapper of the lumpy-using smoove workflow 0
svtyper
To update
2.8+galaxy0 justgzip Compress fastq sequence files 20
pigz
To update
3.10+galaxy0 justdiff Unix diff 0
diffutils
To update
3.1.3+galaxy0 high_dim_heatmap gplot heatmap.2 function adapted for plotting large heatmaps 0
r-gplots
To update
6.5.7+galaxy0 guppy-basecaller A wrapper for the guppy basecaller tool from Oxford Nanopore Technologies 7
To update
2.3.9+galaxy1 signature_score Compute signature scores from single cell RNAseq data RNA-Seq analysis Clustering Visualisation Expression analysis 0
r-optparse
To update
1.28.1+galaxy1 scran_normalize Normalize raw counts using scran RNA-Seq analysis Clustering Visualisation Expression analysis 508
bioconductor-scran
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
4.1.3+galaxy1 mannwhitney_de Perform a mann-whitney differential testing between two sets of gene expression data RNA-Seq analysis Clustering Visualisation Expression analysis 0
r-optparse
To update
4.3+galaxy1 high_dimensions_visualisation Generates PCA, t-SNE and HCPC visualisation RNA-Seq analysis Clustering Visualisation Expression analysis 0
r-optparse
To update
4.3.1+galaxy1 single_cell_gene_expression_correlations Compute single-cell paire-wise gene expressions correlations RNA-Seq analysis Clustering Visualisation Expression analysis 0
r-optparse
To update
4.3.1+galaxy1 filter_genes Filter genes that are detected in less than a fraction of libraries in single cell RNAseq data RNA-Seq analysis Clustering Visualisation Expression analysis 0
r-optparse
To update
4.3.1+galaxy1 filter_cells Filter single cell RNAseq data on library depth and number of detected genes RNA-Seq analysis Clustering Visualisation Expression analysis 0
r-optparse
To update
4.3.1+galaxy1 center_scale Center or scale (standardize) data RNA-Seq analysis Clustering Visualisation Expression analysis 0
r-optparse
To update
0.3.2 get_fasta_reference Obtain reference genome sequence. 0
To update
4.1.7.0 filtermutectcalls mergemutectstats mutect2 Find somatic variations 0
gatk4
To update
2.32.0+galaxy0 fishertest Fisher's exact test on two-column hit lists. 0
bioconductor-qvalue
To update
3.1.0 retrieve_fasta_from_NCBI Fetch fasta sequences from NCBI using eutils wrappers 5
urllib3
To update
3.4.4 ez_histograms ggplot2 histograms and density plots Ecology Data analysis Statistical calculation Visualisation 0
r-ggplot2
To update
0.2 embl2fa Converts EMBL flat format to fasta format 0
To update
1.40.2+galaxy1 deseq2_normalization Normalizes gene hitlists 0
bioconductor-deseq2
To update
0.6.0 cpm_tpm_rpk Generate CPM,TPM or RPK from raw counts 0
r-optparse
To update
1.4.3 cat_multi_datasets Concatenate multiple datasets tail-to-head, including collection datasets. 15438
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
4.1 cherry_pick_fasta Pick fasta sequence with specific header content 0
python
To update
2.0.1 cap3 cap3 wrapper 19100
cap3
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
1.1.1 blastx2scaffold Generate DNA scaffold from blastx alignment of Contigs 0
python
To update
2.7.1 BlastParser_and_hits Parse blast outputs and compile hits 8
python
To update
1.0.1 blast_unmatched Extract unmatched query sequences from blast 0
python
To update
1.1.0 blast2scaffold Generate DNA scaffold from blastn or tblastx alignments of Contigs 8
python
To update
3+galaxy0 bigwig_to_wig Converts a bigWig file to Wiggle (WIG) format 0
ucsc-bigwiginfo
To update
377+galaxy1 bigwig_to_bedgraph Converts a bigWig file to bedGraph format 7955
ucsc-bigwigtobedgraph
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
4.1.1 bamparse Generates hit count lists from bam alignments. 0
pysam
To update
1.10+galaxy0 artbio_bam_cleaning filter bam files before somatic-varscan or lumpy-smoove analysis 0
samtools
To update
vmd
vmd is a package for visualizing and analyzing trajectories from molecular dynamics (MD) simulations 0
To update
1.8.1 pdbfixer OpenMM is a toolkit for molecular simulation using high performance GPU code. 1233
pdbfixer
To update
UseGalaxy.cz1 UseGalaxy.eu1
1.9.7 traj_selections_and_merge MDTraj is a python library that allows users to manipulate molecular dynamics (MD) trajectories 99
mdtraj
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
1.9.9 md_slicer A tool for slicing trajectory files using MDTraj. 666
mdtraj
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
1.9.7 md_converter A tool for interconverting between different MD structure and trajectory file formats. 29245
mdtraj
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
1.0.0 mdanalysis_angle mdanalysis_dihedral mdanalysis_distance mdanalysis_endtoend mdanalysis_extract_rmsd mdanalysis_hbonds mdanalysis_cosine_analysis mdanalysis_ramachandran_protein mdanalysis_ramachandran_plot mdanalysis_rdf MDAnalysis is a package for analyzing trajectories from molecular dynamics (MD) simulations 4201
mdanalysis
To update
UseGalaxy.be1 UseGalaxy.cz10 UseGalaxy.eu10 UseGalaxy.no10 UseGalaxy.or5
2022 gmx_check gmx_editconf gmx_energy gmx_get_builtin_file gmx_rg gmx_makendx gmx_merge_topology_files gmx_em gmx_restraints gmx_rmsd gmx_rmsf gmx_setup gmx_sim gmx_solvate gmx_trj GROMACS is a package for performing molecular dynamics, primarily designed for biochemical molecules such as proteins, lipids and nucleic acids. 214953
gromacs
To update
UseGalaxy.be6 UseGalaxy.cz15 UseGalaxy.eu15 UseGalaxy.no9 UseGalaxy.or8
Free energy tools of BRIDGE. 0
To update
0 gromacs_modify_topology gromacs_extract_topology Set of python scripts and associated tool files that can be used to modify topology files. 88
python
To update
UseGalaxy.cz2 UseGalaxy.eu2 UseGalaxy.or2
18.169.1 packmol PACKMOL is a package for creating starting structures for Molecular Dynamics simulations 722
packmol
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
21.10 ambertools_acpype acpype_Amber2Gromacs ambertools_antechamber mmpbsa_mmgbsa ambertools_parmchk2 parmconv tleap Ambertools is a set of packages for preparing systems for molecular dynamics (MD) simulations and analyzing trajectories. 46482
ambertools
To update
UseGalaxy.be1 UseGalaxy.cz7 UseGalaxy.eu7 UseGalaxy.no5 UseGalaxy.or2
1.5.2 biomd_neqgamma fastpca biomd_extract_clusters biomd_rmsd_clustering Tools for MD analysis 1107
scipy
To update
UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.no3 UseGalaxy.or4
4.2.1 biobb_pytorch_apply_mdae biobb_pytorch_train_mdae biobb_pytorch is the Biobb module collection to create and train ML & DL models using the popular [PyTorch](https://pytorch.org/) Python library. 0
biobb_pytorch
To update
2.4_1 bio3d_dccm bio3d_pca bio3d_rmsd bio3d_rmsf bio3d_pca_visualize Bio3d is a program that can be used to analyse molecular dynamics trajectories. 16285
r-bio3d
To update
UseGalaxy.be4 UseGalaxy.cz5 UseGalaxy.eu5 UseGalaxy.no5 UseGalaxy.or4
2.0.4 ZeissLMDconverter Converts coordinates from a tabular file into a formatted text file readable by Zeiss laser-capture microdissection systems 8
shapely
To update
UseGalaxy.eu1
0.1.5 validate_fasta_database runs Compomics database identification tool on any FASTA database, and separates valid and invalid entries based on a series of checks. 254
validate-fasta-database
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
2.5.0 uniprotxml_downloader Download UniProt proteome in XML or fasta format 2631
requests
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
6.2.4+galaxy0 unipept Unipept retrieves metaproteomics information Proteomics Proteogenomics Biodiversity Workflows Prediction and recognition Visualisation 7083
python
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.2.0 translate_bed_sequences Perform 3 frame translation of BED file augmented with a sequence column 69
biopython
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.1.0 gp_spectrast2tsv Filter from spectraST files to swath input files 0
msproteomicstools
To update
0.1.0 gp_spectrast2spectrast_irt Filter from spectraST files to swath input files 0
msproteomicstools
To update
0.2.4 sixgill_build sixgill_filter sixgill_makefasta sixgill_merge Six-frame Genome-Inferred Libraries for LC-MS/MS 316
sixgill
Up-to-date
UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.no4
0.1.0 scaffold scaffold_export 0
scaffold
To update
1.0.3 regex1 regexColumn1 Use python regular expressions to find and replace text 117062
python
To update
UseGalaxy.be2 UseGalaxy.cz2 UseGalaxy.eu2 UseGalaxy.fr2 UseGalaxy.no2 UseGalaxy.or2
rawtools Raw Tools 660
rawtools
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.3.2 qupath_roi_splitter Split ROI coordinates of QuPath TMA annotation by cell type 181
geojson
To update
UseGalaxy.cz1 UseGalaxy.eu1
2.0 quantwiz_iq Isobaric Quantitation using QuantWiz-IQ 32
quantwiz-iq
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.1.2 quantp Correlation between protein and transcript abundance 242
r-data.table
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1
4.4.1 mztab2tsv Tools using the pyteomics library Proteomics Proteomics experiment Protein identification 92
pyteomics
To update
UseGalaxy.cz1 UseGalaxy.eu1
2.1.4 pyprophet_export pyprophet_merge pyprophet_peptide pyprophet_protein pyprophet_score pyprophet_subsample Semi-supervised learning and scoring of OpenSWATH results. 3435
pyprophet
To update
UseGalaxy.be5 UseGalaxy.cz6 UseGalaxy.eu6 UseGalaxy.no6 UseGalaxy.or5
1.1.2 maxquant_ptxqc Quality control reports for MaxQuant results Proteomics Validation 0
r-ptxqc
To update
1.0.3 psmvalidator Validate PSM from Ion Fragmentation 20
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.1.0 psm_eval 0
binaries_for_psm_eval
To update
0.1.0 protxml_to_xls 0
trans_proteomic_pipeline
To update
2021.06.08 proteore_venn_diagram ProteoRE JVenn Diagram 15
python
To update
0.0.8 proteomiqon_psmstatistics The PSMStatistics tool utilizes semi supervised machine learning techniques to integrate search engine scores as well as the mentioned quality scores into one single consensus score. 694
proteomiqon-psmstatistics
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
0.0.8 proteomiqon_psmbasedquantification The PSMBasedQuantification tool was designed to allow label-free quantification as well as quantification of full metabolic labeled samples. 604
proteomiqon-psmbasedquantification
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.0.7 proteomiqon_proteininference MS-based shotgun proteomics estimates protein abundances using a proxy: peptides. The process of 'Protein Inference' is concerned with the mapping of identified peptides to the proteins they putatively originated from. 89
proteomiqon-proteininference
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
0.0.7 proteomiqon_peptidespectrummatching Given raw an MS run in the mzLite format, this tool iterates across all MS/MS scans, determines precursor charge states and possible peptide spectrum matches using reimplementations of SEQUEST,Andromeda and XTandem. 686
proteomiqon-peptidespectrummatching
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
0.0.7 proteomiqon_peptidedb The tool ProteomIQon PeptideDB creates a peptide database in the SQLite format. 96
proteomiqon-peptidedb
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
0.0.8 proteomiqon_mzmltomzlite The tool MzMLToMzLite allows to convert mzML files to mzLite files. 722
proteomiqon-mzmltomzlite
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
0.0.1 proteomiqon_labelfreeproteinquantification The tool LabelFreeProteinQuantification estimates protein abundances using quantified peptide ions. 8
proteomiqon-labelfreeproteinquantification
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.0.1 proteomiqon_labeledproteinquantification The tool LabeledProteinQuantification estimates protein abundances using quantified peptide ions. 16
proteomiqon-labeledproteinquantification
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.0.1 proteomiqon_joinquantpepionswithproteins The tool JoinQuantPepIonsWithProteins combines results from ProteinInference and PSMBasedQuantification. 372
proteomiqon-joinquantpepionswithproteins
To update
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0.1.0 translate_bed Translate BED transcript CDS or cDNA in 3 frames 2077
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.1.0 retrieve_ensembl_bed Retrieve cDNA features from Ensembl REST API in BED format 0
To update
0.1 convert_windows_newlines proteinpilot proteinpilot_group_extractor proteinpilot_tabular proteinpilot_xml 0
To update
1.3.2.1 PSMtoSAM PSM to SAM 0
r-base
To update
UseGalaxy.fr1
CustomProDB Annotation 0
To update
1.22.0 custom_pro_db CustomProDB 2661
bioconductor-rgalaxy
To update
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1.4.0 pmd_fdr Calculate Precursor Mass Discrepancy (PMD) for MS/MS 0
r-base
To update
1.3 calc_delta_pi pi_db_split pi_dbspec_align HiRIEF tools 0
python
To update
3.5 batched_set_list_creator percolator percolator_input_converters pout2mzid Percolator 1629
percolator
To update
UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.no4 UseGalaxy.or4
Convert PepXML to Tabular 0
To update
fasta_cli ident_params peptide_shaker search_gui PeptideShaker and SearchGUI 23289
searchgui
To update
UseGalaxy.be2 UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.fr4 UseGalaxy.no2 UseGalaxy.or4
1.0.0 peptide_genomic_coordinate Gets genomic coordinate of peptides based on the information in mzsqlite and genomic mapping sqlite files 660
python
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
2.0.2 pepquery2 pepquery2_index pepquery2_show_sets PepQuery2 peptide-centric MS search for peptide identification and validation 1749
pepquery
Up-to-date
UseGalaxy.cz3 UseGalaxy.eu3 UseGalaxy.or1
1.6.2 pepquery A peptide-centric MS search engine for novel peptide identification and validation. 7435
pepquery
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.1.3+galaxy1 pep_pointer PepPointer categorizes peptides by their genomic coordinates. 753
python
To update
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reactome_pathwaymatcher Reactome Pathway Matcher 258
pathwaymatcher
To update
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3.1 AccurateMassSearch AssayGeneratorMetabo BaselineFilter CVInspector ClusterMassTraces ClusterMassTracesByPrecursor CometAdapter ConsensusID ConsensusMapNormalizer DTAExtractor DatabaseFilter DatabaseSuitability DeMeanderize DecoyDatabase Digestor DigestorMotif EICExtractor ERPairFinder Epifany ExternalCalibration FalseDiscoveryRate FeatureFinderCentroided FeatureFinderIdentification FeatureFinderIsotopeWavelet FeatureFinderMRM FeatureFinderMetabo FeatureFinderMetaboIdent FeatureFinderMultiplex FeatureLinkerLabeled FeatureLinkerUnlabeled FeatureLinkerUnlabeledKD FeatureLinkerUnlabeledQT FileConverter FileFilter FileInfo FileMerger FuzzyDiff GNPSExport HighResPrecursorMassCorrector IDConflictResolver IDExtractor IDFileConverter IDFilter IDMapper IDMassAccuracy IDMerger IDPosteriorErrorProbability IDRTCalibration IDRipper IDScoreSwitcher IDSplitter InternalCalibration IsobaricAnalyzer JSONExporter LuciphorAdapter MRMMapper MRMPairFinder MRMTransitionGroupPicker MSFraggerAdapter MSGFPlusAdapter MSstatsConverter MapAlignerIdentification MapAlignerPoseClustering MapAlignerSpectrum MapAlignerTreeGuided MapNormalizer MapRTTransformer MapStatistics MascotAdapter MascotAdapterOnline MassCalculator MassTraceExtractor MetaProSIP MetaboliteSpectralMatcher MultiplexResolver MzMLSplitter MzTabExporter NoiseFilterGaussian NoiseFilterSGolay NovorAdapter NucleicAcidSearchEngine OpenMSDatabasesInfo OpenMSInfo OpenPepXL OpenPepXLLF OpenSwathAnalyzer OpenSwathAssayGenerator OpenSwathChromatogramExtractor OpenSwathConfidenceScoring OpenSwathDIAPreScoring OpenSwathDecoyGenerator OpenSwathFeatureXMLToTSV OpenSwathFileSplitter OpenSwathMzMLFileCacher OpenSwathRTNormalizer OpenSwathRewriteToFeatureXML OpenSwathWorkflow PSMFeatureExtractor PeakPickerHiRes PeakPickerIterative PeakPickerWavelet PeptideIndexer PercolatorAdapter PhosphoScoring PrecursorMassCorrector ProteinInference ProteinQuantifier ProteinResolver QCCalculator QCEmbedder QCExporter QCExtractor QCImporter QCMerger QCShrinker QualityControl RNADigestor RNAMassCalculator RNPxlSearch RNPxlXICFilter SageAdapter SeedListGenerator SemanticValidator SequenceCoverageCalculator SimpleSearchEngine SiriusAdapter SpecLibCreator SpecLibSearcher SpectraFilterBernNorm SpectraFilterMarkerMower SpectraFilterNLargest SpectraFilterNormalizer SpectraFilterParentPeakMower SpectraFilterScaler SpectraFilterSqrtMower SpectraFilterThresholdMower SpectraFilterWindowMower SpectraMerger SpectraSTSearchAdapter StaticModification TICCalculator TOFCalibration TargetedFileConverter TextExporter TriqlerConverter XFDR XMLValidator XTandemAdapter OpenMS Suite for LC/MS data management and analyses 113988
openms
To update
UseGalaxy.be18 UseGalaxy.cz141 UseGalaxy.eu144 UseGalaxy.no124 UseGalaxy.or34
2.1.1+galaxy0 mz_to_sqlite Creates a SQLite database for proteomics data Proteomics Biological databases Conversion Peptide database search 1239
mztosqlite
To update
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1.1.0 mt2mq Tool to prepare metatranscriptomic outputs from ASaiM for Metaquantome 276
r-tidyverse
To update
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2.0.0 msstatstmt MSstatsTMT protein significance analysis in shotgun mass spectrometry-based proteomic experiments with tandem mass tag (TMT) labeling 1410
bioconductor-msstatstmt
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.or1
4.0.0 msstats MSstats tool for analyzing mass spectrometry proteomic datasets Proteomics Proteomics experiment Protein expression Spectrum calculation Tag-based peptide identification Differential protein expression profiling 5259
bioconductor-msstats
To update
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1.0.0 msms_extractor Extract MS/MS scans from the mzML file(s) based on PSM report. 121
proteowizard
To update
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0.5 msgfplus MSGF+ 810
msgf_plus
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
3.0.20287 msconvert msconvert Convert and/or filter mass spectrometry files (including vendor formats) using the official Docker container Proteomics Proteomics experiment Filtering Formatting 75864
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.1.19 mqppep_anova mqppep_preproc MaxQuant Phosphoproteomic Enrichment Pipeline - Preprocessing and ANOVA 13
bioconductor-preprocesscore
To update
UseGalaxy.cz2 UseGalaxy.eu2
288 morpheus Morpheus MS Search Application Proteomics Peptide database search 1197
morpheus
To update
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2.0.3 proteomics_moff moFF (a modest Feature Finder) extracts MS1 intensities from RAW and mzML spectrum files. 944
moff
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
1.0.0 mgf_formatter 0
mgf-formatter
Up-to-date
2.0.2 metaquantome_db metaquantome_expand metaquantome_filter metaquantome_sample metaquantome_stat metaquantome_viz quantitative analysis of microbiome taxonomy and function Proteomics Metatranscriptomics Microbial ecology Proteomics experiment Metagenomics Principal component visualisation Visualisation Functional clustering Query and retrieval Differential protein expression analysis Heat map generation Quantification Indexing Filtering Statistical inference 4904
metaquantome
Up-to-date
UseGalaxy.be6 UseGalaxy.cz6 UseGalaxy.eu6 UseGalaxy.fr6 UseGalaxy.no6 UseGalaxy.or6
1.9.4 metanovo Produce targeted databases for mass spectrometry analysis. Proteomics Microbial ecology Metagenomics Proteomics experiment Small molecules Target-Decoy de Novo sequencing Tag-based peptide identification Protein identification Expression analysis 4956
metanovo
Up-to-date
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1.0 metagene_annotator MetaGeneAnnotator gene-finding program for prokaryote and phage Genomics Model organisms Data submission, annotation and curation Sequence annotation 1198
metagene_annotator
Up-to-date
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2.0.0 meta_proteome_analyzer MetaProteomeAnalyzer 142
mpa-portable
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
2.0.3.0 maxquant maxquant_mqpar wrapper for MaxQuant Proteomics experiment Proteomics Statistics and probability Imputation Visualisation Protein quantification Statistical calculation Standardisation and normalisation Heat map generation Clustering Principal component plotting 14814
maxquant
Up-to-date
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0.2 map_peptides_to_bed Map peptides to a reference genome for display by a genome browser 46
biopython
To update
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1.22.0 maldi_quant_peak_detection maldi_quant_preprocessing MALDIquant provides a complete analysis pipeline for MALDI-TOF and other 2D mass spectrometry data. 5040
r-base
To update
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0
To update
1.0 lfq_protein_quant Enable protein summarisation and quantitation 116
bioconductor-msnbase
To update
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4.1+galaxy0 iedb_netmhciipan iedb_netmhcpan Predict binding of peptides to any MHC or MHC II molecule of known sequence using artificial neural networks 0
To update
UseGalaxy.eu2
idconvert Convert mass spectrometry identification files on linux or MacOSX 277
proteowizard
To update
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2.30.1+galaxy1 hardklor kronik Hardklör 111
hardklor
To update
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0.2.1 gffcompare_to_bed Filter and convert a gffCompare GTF to BED 4001
python
To update
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20.0 fragpipe Data analysis for mass spectrometry-based proteomics. 210
fragpipe
To update
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1.0.3.1 flashlfq FlashLFQ mass-spectrometry proteomics label-free quantification Proteomics experiment Proteomics Label-free quantification 911
flashlfq
To update
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2.3 filter_by_fasta_ids Filter FASTA on the headers and/or the sequences 169301
python
To update
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0.11.0 feature_alignment TRIC integrates information from all available runs via a graph-based alignment strategy 18
msproteomicstools
Up-to-date
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1.0.2 fastg2protlib-peptides fastg2protlib-validate Generate FASTA from FASTG 29
To update
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1.2.0 fasta_merge_files_and_filter_unique_sequences Concatenate FASTA database files together 78421
python
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
1.12.34 encyclopedia_encyclopedia encyclopedia_fasta_to_prosit_csv encyclopedia_library_to_blib encyclopedia_prosit_csv_to_library encyclopedia_quantify encyclopedia_searchtolib encyclopedia_walnut Mass Spec Data-Independent Acquisition (DIA) MS/MS analysis 857
encyclopedia
To update
UseGalaxy.cz7 UseGalaxy.eu7 UseGalaxy.or4
2.1.8 eggnog_mapper eggnog_mapper_annotate eggnog_mapper_search eggnog-mapper fast functional annotation of novel sequences Metagenomics Phylogeny Transcriptomics Workflows Sequence analysis Homology-based gene prediction Genome annotation Fold recognition Information extraction Query and retrieval 128641
eggnog-mapper
To update
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download eggnog data for eggnog-mapper 0
To update
downloads eggnog data for eggnog-mapper 0
To update
0
To update
0.1.0 digestdb 0
trans_proteomic_pipeline
To update
1.0.6 diffacto Diffacto comparative protein abundance estimation 11
diffacto
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.3.5.0 diapysef diapysef is a convenience package for working with DIA-PASEF data 585
diapysef
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
1.8.1 diann DiaNN (DIA-based Neural Networks) is a software for DIA/SWATH data processing. 351
To update
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1.2.0 dialignr DIAlignR is an R package for retention time alignment of targeted mass spectrometric data, including DIA and SWATH-MS data. This tool works with MS2 chromatograms directly and uses dynamic programming for alignment of raw chromatographic traces. DIAlignR uses a hybrid approach of global (feature-based) and local (raw data-based) alignment to establish correspondence between peaks. 40
bioconductor-dialignr
To update
UseGalaxy.cz1 UseGalaxy.eu1
2.1.3 dia_umpire_se DIA-Umpire analysis for data independent acquisition (DIA) mass spectrometry-based proteomics 188
dia_umpire
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
Galaxy tool wrapper for the transproteomic pipeline decoyFASTA tool. 0
To update
0.3.4 dbbuilder Protein Database Downloader 8363
wget
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
3.4.3 cardinal_classification cardinal_colocalization cardinal_combine cardinal_data_exporter cardinal_filtering cardinal_mz_images cardinal_preprocessing cardinal_quality_report cardinal_segmentations cardinal_single_ion_segmentation cardinal_spectra_plots Statistical and computational tools for analyzing mass spectrometry imaging datasets 59499
bioconductor-cardinal
To update
UseGalaxy.be9 UseGalaxy.cz11 UseGalaxy.eu11 UseGalaxy.fr11 UseGalaxy.no9 UseGalaxy.or9
3.0.13 calisp Calgary approach to isotopes in proteomics 223
calisp
To update
UseGalaxy.cz1 UseGalaxy.eu1
3.0.21142 idpqonvertEmbedder idpassemble idpqonvert idpquery myrimatch 1439
bumbershoot
To update
UseGalaxy.cz5 UseGalaxy.eu5 UseGalaxy.no5
2.6.0 blast_plus_remote_blastp NCBI BLAST+ with -remote option 0
blast
To update
0.2.0 bed_to_protein_map Converts a BED file to a tabular list of exon locations 993
python
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.2.0 append_fdr 0
To update
1.3.4 thermo_raw_file_converter Thermo RAW file converter Proteomics Proteomics experiment Metabolomics Conversion Filtering Peak detection 4213
thermorawfileparser
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
vcfvcfintersect Intersect two VCF datasets 1084461
vcflib
To update
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vcfsort Sort VCF dataset by coordinate 28056
vcflib
To update
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vcfselectsamples Select samples from a VCF file 7655
vcflib
To update
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vcfrandomsample Randomly sample sites from VCF dataset 739
vcflib
To update
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vcfprimers Extract flanking sequences for each VCF record 1806
vcflib
To update
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vcfleftalign Left-align indels and complex variants in VCF dataset 2080
vcflib
To update
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vcfhethom Count the number of heterozygotes and alleles, compute het/hom ratio. 6694
vcflib
To update
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vcfgenotypes Convert numerical representation of genotypes to allelic. 8101
vcflib
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vcfgeno2haplo Convert genotype-based phased alleles into haplotype alleles 4863
vcflib
To update
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vcfflatten2 Removes multi-allelic sites by picking the most common alternate 1488
vcflib
To update
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vcffixup Count the allele frequencies across alleles present in each record in the VCF file. 6682
vcflib
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
vcffilter2 Tool for filtering VCF files 221503
vcflib
To update
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vcfdistance Calculate distance to the nearest variant. 3349
vcflib
To update
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vcfcommonsamples Output records belonging to samples commong between two datasets. 2385
vcflib
To update
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vcfcombine Combine multiple VCF datasets 22714
vcflib
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vcfcheck Verify that the reference allele matches the reference genome 3851
vcflib
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vcfbreakcreatemulti Break multiple alleles into multiple records, or combine overallpoing alleles into a single record 11403
vcflib
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vcfbedintersect Intersect VCF and BED datasets 25498
vcflib
To update
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vcfannotategenotypes Annotate genotypes in a VCF dataset using genotypes from another VCF dataset. 2274
vcflib
To update
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vcfannotate Intersect VCF records with BED annotations 18316
vcflib
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vcfallelicprimitives Splits alleleic primitives (gaps or mismatches) into multiple VCF lines 35753
vcflib
To update
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vcfaddinfo Adds info fields from the second dataset which are not present in the first dataset. 10094
vcflib
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vcf2tsv Converts VCF files into tab-delimited format 219658
vcflib
To update
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snpSift_geneSets Annotate SnpEff vcf with genesets such as Gene Ontology (GO), KEGG, Reactome 1068
snpsift
To update
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snpSift_dbnsfp snpEff SnpSift dbnsfp tool from Pablo Cingolani 478
snpsift
To update
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snpSift_annotate snpSift_caseControl snpSift_extractFields snpSift_filter snpSift_int snpSift_rmInfo snpsift_vartype snpSift_vcfCheck snpEff SnpSift tools from Pablo Cingolani 5705944
snpsift
To update
UseGalaxy.be8 UseGalaxy.cz8 UseGalaxy.eu8 UseGalaxy.fr8 UseGalaxy.no8 UseGalaxy.or8
5.2 snpEff snpEff_build_gb snpEff_databases snpEff_download snpEff_get_chr_names SnpEff is a genetic variant annotation and effect prediction toolbox 332870
biopython
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UseGalaxy.be5 UseGalaxy.cz5 UseGalaxy.eu5 UseGalaxy.fr5 UseGalaxy.no5 UseGalaxy.or5
1.22 0
samtools
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2.1.3 kraken2 Kraken2 for taxonomic designation. Taxonomy Metagenomics Microbial ecology Microbiology Taxonomic classification 618635
kraken2
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kraken-filter kraken-mpa-report kraken-report kraken-translate kraken Kraken is a system for assigning taxonomic labels to short DNAsequences, usually obtained through metagenomic studies. Previous attempts by otherbioinformatics software to accomplish this task have often used sequence alignmentor machine learning techniques that were quite slow, leading to the developmentof less sensitive but much faster abundance estimation programs. Kraken aims toachieve high sensitivity and high speed by utilizing exact alignments of k-mersand a novel classification algorithm. Taxonomy Metagenomics Taxonomic classification 233430
kraken
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1.1.5 tabular_to_fastq Tabular to FASTQ converter 43794
galaxy_sequence_utils
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1.1.5 fastq_to_fasta_python FASTQ to FASTA converter 537669
galaxy_sequence_utils
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1.1.5 fastq_trimmer FASTQ Trimmer by quality 108756
galaxy_sequence_utils
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1.1.5 fastq_to_tabular FASTQ to Tabular converter 57737
galaxy_sequence_utils
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1.1.5 fastq_stats FASTQ Summary Statistics by column 91994
galaxy_sequence_utils
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1.1.5 fastq_paired_end_splitter FASTQ splitter on joined paired end reads 45492
galaxy_sequence_utils
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1.1.5 fastq_paired_end_joiner FASTQ joiner on paired end reads 80045
galaxy_sequence_utils
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1.1.5 fastq_paired_end_interlacer FASTQ interlacer on paired end reads 56567
galaxy_sequence_utils
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1.1.5 fastq_paired_end_deinterlacer FASTQ de-interlacer on paired end reads. 33865
galaxy_sequence_utils
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1.1.5 fastq_masker_by_quality FASTQ Masker by quality score 9032
galaxy_sequence_utils
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1.1.5 fastq_manipulation Manipulate FASTQ reads on various attributes. 22838
galaxy_sequence_utils
To update
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1.1.5 fastq_groomer Convert between various FASTQ quality formats. 1054852
galaxy_sequence_utils
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1.1.5 fastq_filter Filter FASTQ reads by quality score and length 153167
galaxy_sequence_utils
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1.1.5 fastq_combiner Combine FASTA and QUAL into FASTQ 87437
galaxy_sequence_utils
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0.0.14 cshl_fastx_trimmer Trim sequences 236326
fastx_toolkit
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0.0.14 cshl_fastx_reverse_complement Reverse-Complement 87246
fastx_toolkit
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0.0.14 cshl_fastx_renamer Rename sequences 19621
fastx_toolkit
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0.0.14 cshl_fastx_quality_statistics Compute quality statistics 71021
fastx_toolkit
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0.0.14 cshl_fastx_nucleotides_distribution Draw nucleotides distribution chart 27103
fastx_toolkit
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0.0.14 cshl_fastx_collapser Collapse sequences 298389
fastx_toolkit
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0.0.14 cshl_fastx_clipper Clip adapter sequences 123635
fastx_toolkit
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0.0.14 cshl_fastx_barcode_splitter Barcode Splitter 124269
fastx_toolkit
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0.0.14 cshl_fastx_artifacts_filter Remove sequencing artifacts 29175
fastx_toolkit
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0.0.14 cshl_fastq_to_fasta FASTQ to FASTA converter 168967
fastx_toolkit
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0.0.14 cshl_fastq_quality_filter Filter by quality 187994
fastx_toolkit
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0.0.14 cshl_fastq_quality_converter Quality format converter (ASCII-Numeric) 11473
fastx_toolkit
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0.0.14 cshl_fastq_quality_boxplot Draw quality score boxplot 62010
fastx_toolkit
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0.0.14 cshl_fasta_nucleotides_changer RNA/DNA converter. 6926
fastx_toolkit
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0.0.14 cshl_fasta_formatter FASTA Width formatter 38903
fastx_toolkit
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0.0.14 cshl_fasta_clipping_histogram Length Distribution chart 5786
fastx_toolkit
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2.2.1 cuffquant The Cuffquant tool 17093
cufflinks
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2.2.1 cuffnorm The Cuffnorm tool 14558
cufflinks
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2.2.1 cuffmerge Galaxy wrappers for the Cuffmerge tool. 74794
cufflinks
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2.2.1 cufflinks Galaxy wrappers for the Cufflinks tool. 398335
cufflinks
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2.2.1 cuffdiff Galaxy wrappers for the Cuffdiff tool. 128374
cufflinks
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2.2.1 cuffcompare Galaxy wrappers for the Cuffcompare tool. 27088
cufflinks
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1.4.5 bacteria_tradis tradis_essentiality tradis_gene_insert_sites Bio-Tradis is a tool suite dedicated to essentiality analyses with TraDis data. Mobile genetic elements Workflows Sequence analysis 6465
biotradis
Up-to-date
UseGalaxy.or3
2.5.2 bamtools_split_mapped bamtools_split_paired bamtools_split_ref bamtools_split_tag Utility for filtering BAM files. It is based on the BAMtools suiteof tools by Derek Barnett. Sequencing Data management Sequence analysis Data handling Sequence alignment analysis 25660
bamtools
To update
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2.5.2 bamFilter Filter BAM datasets on various attributes using bamtools filter Sequencing Data management Sequence analysis Data handling Sequence alignment analysis 291365
bamtools
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2.5.2 bamtools Operate on and transform BAM datasets in various ways using bamtools Sequencing Data management Sequence analysis Data handling Sequence alignment analysis 117874
bamtools
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1.0 zerone ChIP-seq discretization and quality control 96
zerone
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1.2a.2 yahs Yet Another Hi-C scaffolding tool 1929
yahs
To update
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xpath XPath XML querying tool 237
perl-xml-xpath
To update
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2.03 winnowmap A long-read mapping tool optimized for mapping ONT and PacBio reads to repetitive reference sequences. 373
winnowmap
Up-to-date
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1.0 windowmasker_mkcounts windowmasker_ustat Identify repetitive regions using WindowMasker 1902
blast
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3.5.0 rgweblogo3 Sequence Logo generator for fasta Nucleic acid sites, features and motifs Sequence analysis Sequence cluster visualisation Sequence visualisation Sequence motif recognition 35167
weblogo
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0.1.2 simple_weather provides simple weather in text format 0
curl
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3.0.6 vsnp_add_zero_coverage vsnp_build_tables vsnp_determine_ref_from_data vsnp_get_snps vsnp_statistics The vSNP tools are critical components of several workflows that validate SNPs and produce annotatedSNP tables and corresponding phylogenetic trees. 0
pysam
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2.8.3 vsearch_alignment vsearch_chimera_detection vsearch_clustering vsearch_dereplication vsearch_masking vsearch_search vsearch_shuffling vsearch_sorting VSEARCH including searching, clustering, chimera detection, dereplication, sorting, masking and shuffling of sequences. Metagenomics Sequence analysis DNA mapping Chimera detection 76088
vsearch
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3.5.2 volcanoplot Tool to create a Volcano Plot 110713
r-ggplot2
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1.1.1 virulign A tool for codon-correct pairwise alignments, with an augmented functionality to annotate the alignment according the positions of the proteins. 0
virulign
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1.0.0 virhunter Deep Learning method for novel virus detection in sequencing data Virology Sequence classification 760
numpy
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0.7.1 virheat generates a heatmap of allele frequencies from vcf files 15
virheat
To update
UseGalaxy.eu1
1.2.0 virannot_blast2tsv virannot_otu virAnnot_rps2tsv virAnnot wrappers Metagenomics Virology Microbial ecology Sequence annotation Sequence clustering Sequence cluster visualisation 285
biopython
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1.1 viralverify Contigs prediction as viral, chromosomal, plasmidic or uncertain. 0
viralverify
Up-to-date
UseGalaxy.fr1
vg
1.23.0 vg_convert vg_deconstruct vg_view Variation graph data structures, interchange formats, alignment, genotyping, and variant calling methods 479
vg
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1.3.1 verkko Telomere-to-telomere assembly pipeline 130
verkko
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2.2.6+galaxy2 velvetoptimiser Automatically optimize Velvet assemblies Genomics Sequence assembly Optimisation and refinement Sequence assembly 21631
velvet
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velvetg velveth de novo genomic assembler specially designed for short read sequencing technologies Sequence assembly Formatting De-novo assembly 113927
velvet
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0.17.17 velocyto_cli Velocyto is a library for the analysis of RNA velocity. RNA-Seq analysis Splicing analysis 235
velocyto.py
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2.4-3 vegan_diversity vegan_fisher_alpha vegan_rarefaction an R package fo community ecologist Ecology Phylogenetics Environmental science Standardisation and normalisation Analysis 8041
r-vegan
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0.3.7 vcfanno Annotate VCF files Genetic variation Data submission, annotation and curation SNP annotation 1187
vcfanno
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1.6.21 vcf2maf vcf2maf: Convert VCF into MAF 1498
vcf2maf
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1.2.2 varvamp Variable VirusAMPlicons (varVAMP) is a tool to design primers for highly diverse viruses Virology Probes and primers PCR primer design 438
varvamp
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2.4.3 varscan_copynumber varscan_mpileup varscan_somatic VarScan is a variant caller for high-throughput sequencing data 33107
varscan
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2.0.0 mut2read mut2sscs read2mut Collection of tools for analyzing variants in duplex consensus sequencing (DCS) data 652
matplotlib
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1.8.3 vardict_java VarDict - calls SNVs and indels for tumour-normal pairs 387
python
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1.0.3 vapor Classify Influenza samples from raw short read sequence data Whole genome sequencing Mapping Sequence assembly Data retrieval De-novo assembly Read mapping 72539
vapor
Up-to-date
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valet A pipeline for detecting mis-assemblies in metagenomic assemblies. Metagenomics Sequence assembly Sequence assembly Sequence assembly visualisation 938
valet
To update
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0.2.1 usher_matutils usher UShER toolkit wrappers Phylogeny Evolutionary biology Cladistics Genotype and phenotype Phylogenomics Classification Phylogenetic tree visualisation Phylogenetic inference (from molecular sequences) 1060
usher
To update
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1.4.0 rcx_upsetplot Upset plot visualization tool using UpSetR 0
r-upsetr
To update
0.5.1 unicycler Unicycler is a hybrid assembly pipeline for bacterial genomes. Microbiology Genomics Sequencing Sequence assembly Genome assembly Aggregation 203161
unicycler
Up-to-date
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1.1.6 umi_tools_count umi_tools_dedup umi_tools_extract umi_tools_group umi_tools_whitelist UMI-tools extract - Extract UMIs from fastq NGS Sequence sites, features and motifs Quality affairs Sequencing quality control 96352
umi_tools
Up-to-date
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482 ucsc_wigtobigwig converts bedGraph (wig) files into binary bigwig Sequence analysis 8878
ucsc-wigtobigwig
Up-to-date
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482 ucsc_nettoaxt Convert net (and chain) to axt format. Sequence analysis 8
ucsc-nettoaxt
Up-to-date
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482 ucsc_netsyntenic Add synteny info to a net dataset Sequence analysis 23
ucsc-netsyntenic
Up-to-date
UseGalaxy.or1
482 ucsc_netfilter Filter out parts of net Sequence analysis 9
ucsc-netfilter
Up-to-date
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482 ucsc_chainsort Sort chains. By default sorts by score. Sequence analysis 13
ucsc-chainsort
Up-to-date
UseGalaxy.or1
482 ucsc_chainprenet Remove chains that don't have a chance of being netted Sequence analysis 13
ucsc-chainprenet
Up-to-date
UseGalaxy.or1
482 ucsc_chainnet Make alignment nets out of chains Sequence analysis 14
ucsc-chainnet
Up-to-date
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482 ucsc_chainantirepeat Remove repeated chains Sequence analysis 0
ucsc-chainantirepeat
Up-to-date
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482 ucsc_axtomaf Convert dataset from axt to MAF format. Sequence analysis 12
ucsc-axttomaf
Up-to-date
UseGalaxy.or1
482 ucsc_axtchain Chain together genome alignments Sequence analysis 11
ucsc-axtchain
Up-to-date
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482 ucsc-twobittofa twoBitToFa is a tool to convert all or part of .2bit file to FASTA Sequence analysis 1434
ucsc-twobittofa
Up-to-date
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482 ucsc_mafaddirows ucsc_mafcoverage ucsc_maffetch ucsc_mafFilter ucsc_maffrag ucsc_maffrags Utilities for working with MAF (Multiple Alignment Format) files from UCSC 0
ucsc-mafaddirows
Up-to-date
482 maftoaxt Convert dataset from MAF to axt format Sequence analysis 9
ucsc-maftoaxt
Up-to-date
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482 fatovcf Convert a FASTA alignment file to Variant Call Format (VCF) single-nucleotide diffs Sequence analysis 1351
ucsc-fatovcf
Up-to-date
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482 fasplit faSplit is a tool to split a single FASTA file into several files Sequence analysis 11964
ucsc-fasplit
Up-to-date
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482 ucsc_blat Standalone blat sequence search command line tool Sequence analysis Sequence alignment 0
ucsc-blat
Up-to-date
1.30.0 tximport Wrapper for the Bioconductor package tximport Transcriptomics Gene transcripts Workflows Pathway or network analysis Formatting RNA-Seq analysis 9474
bioconductor-tximport
To update
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0.0.2 tsne T-Distributed Stochastic Neighbor Embedding using a Barnes-Hut Implementation 684
r-rtsne
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1.1.2.5 tsebra This tool has been developed to combine BRAKER predictions. Gene expression RNA-Seq Gene transcripts Model organisms Homology-based gene prediction Alternative splicing prediction 43
tsebra
Up-to-date
UseGalaxy.eu1 UseGalaxy.fr1
0.5.5 trycycler_cluster trycycler_consensus trycycler_partition trycycler_reconcile_msa trycycler_subsample Trycycler toolkit wrappers Sequence assembly DNA Human biology Whole genome sequencing Genomics Genome assembly Sequence trimming Scaffold gap completion Sequence assembly validation 20075
trycycler
Up-to-date
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3.2.2 trinotate Trinotate is a comprehensive annotation suite designed for automatic functional annotation of de novo transcriptomes. Gene expression Transcriptomics Gene functional annotation 5478
trinotate
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2.15.1 trinity_abundance_estimates_to_matrix trinity_align_and_estimate_abundance trinity_analyze_diff_expr trinity_contig_exn50_statistic trinity_define_clusters_by_cutting_tree describe_samples trinity_filter_low_expr_transcripts trinity_gene_to_trans_map trinity_run_de_analysis trinity_samples_qccheck trinity_super_transcripts trinity trinity_stats Trinity represents a method for the efficient and robust de novo reconstruction of transcriptomes from RNA-seq datahttps://github.com/trinityrnaseq/trinityrnaseq Transcriptomics Gene expression Gene transcripts Transcriptome assembly 122927
trinity
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0.39 trimmomatic A flexible read trimming tool for Illumina NGS data 1529410
trimmomatic
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1.5.0 trimal Tool for automated alignment trimming Sequence analysis Sequencing Sequence sites, features and motifs Multiple sequence alignment 1072
trimal
Up-to-date
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transtermhp Finds rho-independent transcription terminators in bacterial genomes Transcription factors and regulatory sites Transcriptional regulatory element prediction 652
transtermhp
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3.2.3 gff_to_prot transit_gumbel transit_hmm transit_resampling transit_tn5gaps TRANSIT DNA Sequencing Mobile genetic elements Transposon prediction 5375
transit
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5.5.0 transdecoder TransDecoder finds coding regions within transcripts Genomics Gene transcripts RNA-Seq Gene expression Sequence assembly Whole genome sequencing Coding region prediction de Novo sequencing De-novo assembly 17172
transdecoder
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0.7.8 tracy_align tracy_assemble tracy_basecall tracy_decompose A suite tools for basecalling, alignment, assembly and deconvolution of Sanger chromatograms using tracy. 3649
tracy
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0.1.4 tracegroomer TraceGroomer is a solution for formatting and normalising Tracer metabolomics given file(s), to produce the .csv files which are ready for DIMet tool. 52
tracegroomer
Up-to-date
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1.0.0 tooldistillator tooldistillator_summarize ToolDistillator extract and aggregate information from different tool outputs to JSON parsable files Microbiology Bioinformatics Sequence analysis Data parsing 7899
tooldistillator
Up-to-date
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1.0.15 tn93_readreduce tn93 tn93_cluster tn93_filter Compute distances between sequences 4530
tn93
Up-to-date
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1.1 tetyper Type a specific transposable element (TE) of interest from paired-end sequencing data. 276
tetyper
Up-to-date
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2.2.3 tetoolkit_tetranscripts The TEToolkit suite improves the bioinformatic analysis of repetitive sequences, particularly transposable elements, in order to elucidate novel (and previously ignored) biological insights of their functions in development and diseases. 1246
tetranscripts
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5.5.1 tesseract Tesseract is an OCR engine with support for unicode and the ability to recognize more than 100 languages out of the box. 0
tesseract
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1.0.3 telescope_assign Single locus resolution of Transposable ELEment expression. RNA-Seq Transcriptomics Mapping Gene transcripts Sequence assembly Essential dynamics Sequence trimming RNA-Seq quantification Expression analysis Read mapping 0
telescope
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1.0.1 te_finder Transposable element insertions finder Sequencing Mobile genetic elements Workflows Evolutionary biology Genetic variation Genome indexing Variant calling PCR primer design 209
samtools
To update
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1.0.1 tbvcfreport Generate HTML report from SnpEff M.tuberculosis VCF(s) 16372
tbvcfreport
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1.2 tbl2gff3 Table to GFF3 3195
bcbiogff
To update
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0.4.0 tb_variant_filter M. tuberculosis H37Rv VCF filter 65699
tb_variant_filter
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6.6.5 tb_profiler_collate tb_profiler_profile Processes M. tuberculosis sequence data to infer strain type and identify known drug resistance markers. Antimicrobial resistance prediction 27667
tb-profiler
Up-to-date
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0.7.0 taxpasta standardise taxonomic profiles Taxonomy Metagenomics Standardisation and normalisation Aggregation Formatting Conversion 90
taxpasta
Up-to-date
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2.7.1+galaxy0 taxonomy_krona_chart Krona pie chart from taxonomic profile Metagenomics Visualisation 86851
krona
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0.3.0 taxonomy_filter_refseq Filter RefSeq by taxonomy 0
rust-ncbitaxonomy
To update
0.20.0 name2taxid profile2cami TaxonKit - A Practical and Efficient NCBI Taxonomy Toolkit Taxonomy Biotechnology Ecology Formatting Data retrieval 410
taxonkit
Up-to-date
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1.0.9 tasmanian_mismatch Analysis of positional mismatches 276
tasmanian-mismatch
Up-to-date
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1.0.2 tag_pileup_frequency Contains a tool that generates a frequency pileup of the 5' ends of aligned reads in a BAM filerelative to reference points in a BED file. 1034
openjdk
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1.2.4 table_compute Perform general-purpose table operations 257027
pandas
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1.7.1 syri Synteny and Rearrangement Identifier DNA polymorphism Sequence assembly DNA structural variation Mapping Sequencing Haplotype mapping Variant calling Genotyping Sequence assembly Read mapping 7
syri
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1.0 syndiva SynDivA was developed to analyze the diversity of synthetic libraries of a Fibronectin domain. 30
clustalo
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1.0 swiftlink Parallel MCMC Linkage Analysis 0
swiftlink
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0.6.94 structureharvester for parsing STRUCTURE outputs and for performing the Evanno method 0
structureharvester
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2.3.4 structure for using multi-locus genotype data to investigate population structure. Population genetics Genetic variation analysis 3814
structure
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2.2.3 stringtie stringtie_merge StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts. Transcriptomics RNA-Seq Transcriptome assembly RNA-Seq analysis 655188
stringtie
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2.9.10 strelka_germline strelka_somatic Strelka2 is a fast and accurate small variant caller optimizedfor analysis of germline variation in small cohorts and somaticvariation in tumor/normal sample pairs. The germline caller employs anefficient tiered haplotype model to improve accuracy and provide read-backedphasing, adaptively selecting between assembly and a faster alignment-basedhaplotyping approach at each variant locus. The germline caller also analyzesinput sequencing data using a mixture-model indel error estimation method toimprove robustness to indel noise. The somatic calling model improves on theoriginal Strelka method for liquid and late-stage tumor analysis by accountingfor possible tumor cell contamination in the normal sample. A final empiricalvariant re-scoring step using random forest models trained on various callquality features has been added to both callers to further improve precision. 2593
strelka
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3.2.2 straindesign_analyzing_model straindesign_reduce_model straindesign_simulate_deletion Toolbox to optimize biological model 0
straindesign
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0.11.0 staramr_search Scan genome contigs against the ResFinder, PlasmidFinder, and PointFinder antimicrobial resistance databases. Microbiology Public health and epidemiology Infectious disease Antimicrobial resistance prediction 51323
staramr
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0.5.4-3+galaxy1 star_fusion STAR Fusion detects fusion genes in RNA-Seq data after running RNA-STAR 4813
star-fusion
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2.55 stacks2_clonefilter stacks2_cstacks stacks2_denovomap stacks2_gstacks stacks2_kmerfilter stacks2_populations stacks2_procrad stacks2_refmap stacks2_shortreads stacks2_sstacks stacks2_tsv2bam stacks2_ustacks Stacks is a software pipeline for building loci from short-read sequences, such as RAD-seq 29267
stacks
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stacks_assembleperead stacks_clonefilter stacks_cstacks stacks_denovomap stacks_genotypes stacks_populations stacks_procrad stacks_pstacks stacks_refmap stacks_rxstacks stacks_sstacks stacks_stats stacks_ustacks Stacks is a software pipeline for building loci from short-read sequences, such as RAD-seq Mapping Population genetics Data handling 18086
stacks
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0.2.0 srst2 SRST2 Short Read Sequence Typing for Bacterial Pathogens Whole genome sequencing Public health and epidemiology Comparative genomics Multilocus sequence typing 387
samtools
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3.1.1 fasterq_dump fastq_dump sam_dump NCBI Sequence Read Archive toolkit utilities DNA Genomics Sequencing Data handling 1184364
sra-tools
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1.0.13 squirrel_phylo squirrel_qc QC and Phylogenetic analysis of MPXV Virology Phylogenetic analysis Sequencing quality control 0
squirrel
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0.1.2 spyboat Wavelet analysis for 3d-image stacks 154
spyboat
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2.1 spotyping SpoTyping allows fast and accurate in silico Mycobacterium spoligotyping from sequence reads Microbiology Sequencing Sequence composition, complexity and repeats Genetic variation Variant pattern analysis 1884
spotyping
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0.1.5 spapros_evaluation spapros_selection Select and evaluate probe sets for targeted spatial transcriptomics. Primer and probe design Visualisation 3
spapros
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2.4.9 list_spaln_tables spaln Spaln (space-efficient spliced alignment) maps and aligns a set of cDNA or protein sequences onto a whole genomic sequence. 4911
python
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4.2.0 spades_biosyntheticspades spades_coronaspades spades_metaplasmidspades metaspades spades_metaviralspades spades_plasmidspades rnaspades spades_rnaviralspades spades SPAdes is an assembly toolkit containing various assembly pipelines. It implements the following 4 stages: assembly graph construction, k-bimer adjustment, construction of paired assembly graph and contig construction. Sequence assembly Genome assembly 304417
spades
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2.2.1 spacexr_cside spacexr_rctd Cell type identification and cell type-specific differential expression in spatial transcriptomics 0
r-spacexr
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20210201 sonneityping Scripts for parsing Mykrobe predict results for Shigella sonnei. Whole genome sequencing Genotype and phenotype Genetic variation Metagenomics Antimicrobial resistance prediction Variant calling Genotyping 1
sonneityping
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2.1.7 socru Order and orientation of complete bacterial genomes 974
socru
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1.0 snpfreqplot A plotting app to visualise the SNPs across a region 6778
r-base
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snpeff_sars_cov_2 SnpEff, the COVID-19 version, is a genetic variant annotation and effect prediction toolbox DNA polymorphism Genetic variation Nucleic acid sites, features and motifs SNP detection 898538
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2.5.1 snp_sites Finds SNP sites from a multi-FASTA alignment file 11485
snp-sites
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0.8.2 snp_dists Compute pairwise SNP distance matrix from a FASTA sequence alignment 15393
snp-dists
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snippy_core snippy snippy_clean_full_aln Contains the snippy tool for characterising microbial snps Genomics Model organisms DNA polymorphism Phylogenetics Phylogenetic tree visualisation Phylogenetic tree generation Variant calling 315480
snippy
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1.6 snipit Summarise snps relative to a reference sequence Virology Base position variability plotting 1039
snipit
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2.5.2 sniffles Galaxy wrapper for sniffles DNA structural variation Sequencing Sequence analysis Structural variation detection 5140
sniffles
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2.6.4 snapatac2_clustering snapatac2_peaks_and_motif snapatac2_plotting snapatac2_preprocessing SnapATAC2 – A Python/Rust package for single-cell epigenomics analysis Epigenomics Cell biology Chromosome conformation capture Mapping Sequencing Essential dynamics Dimensionality reduction Gene expression profiling 2841
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2013_11_29 snap snap_training SNAP is a general purpose gene finding program suitable for both eukaryotic and prokaryotic genomes. DNA DNA polymorphism Genetics Gene prediction 3064
snap
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0.2.5 smudgeplot Inference of ploidy and heterozygosity structure using whole genome sequencing Sequence assembly Genetic variation Mathematics Sequence trimming Genotyping k-mer counting 1760
smudgeplot
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0.5.2 smgu_frameshift_deletions_checks Set of utilities for manipulating small viral genome data. Genomics Population genetics Workflows Virology Sequencing Read pre-processing Sequence alignment Genetic variation analysis 159
smallgenomeutilities
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0.30.2 sleuth Sleuth is a program for differential analysis of RNA-Seq data. RNA-Seq Gene expression Statistics and probability Expression data visualisation Differential gene expression analysis Gene expression profiling Statistical calculation 181
r-sleuth
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0.4.3 alleyoop slamdunk Slamdunk maps and quantifies SLAMseq reads 1528
slamdunk
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0.10.1 sinto_barcode sinto_fragments Sinto single-cell analysis tools Bioinformatics Cell biology 633
sinto
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1.7.2 sina SINA reference based multiple sequence alignment Sequencing RNA Nucleic acid structure analysis Taxonomy Sequence analysis Taxonomy Sequence alignment analysis Multiple sequence alignment Taxonomic classification Structure-based sequence alignment 3894
sina
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0.0.2 abstracts_by_pmids pmids_to_pubtator_matrix pubmed_by_queries text_to_wordmatrix A text mining framework for interactive analysis and visualization of similarities among biomedical entities. 734
r-argparse
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1.33.3 sickle A windowed adaptive trimming tool for FASTQ files using quality Data quality management Sequence trimming 31761
sickle-trim
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1.1.0 shovill Faster de novo assembly pipeline based around Spades Genomics Microbiology Sequence assembly Genome assembly 134991
shovill
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1.1.3 shorah_amplicon Reconstruct haplotypes using ShoRAH in amplicon mode Metagenomics Sequencing Genetics Haplotype mapping Variant calling 0
shorah
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0.6.0 shasta Fast de novo assembly of long read sequencing data 1810
shasta
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2.2.0 sfold Predict the probable RNA secondary structures through structure ensemble sampling 0
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5.0 seurat_create seurat_data seurat_integrate seurat_clustering seurat_preprocessing seurat_plot seurat_reduce_dimension Seurat - R toolkit for single cell genomics RNA-Seq Transcriptomics 2967
r-seurat
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0.7.5 seqwish Alignment to variation graph inducer 271
seqwish
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1.0.1 sequali Fast sequencing data quality metrics for short and long reads Data quality management Sequence analysis Sequencing quality control Statistical calculation 0
sequali
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1.5 seqtk_comp seqtk_cutN seqtk_dropse seqtk_fqchk seqtk_hety seqtk_listhet seqtk_mergefa seqtk_mergepe seqtk_mutfa seqtk_randbase seqtk_sample seqtk_seq seqtk_subseq seqtk_telo seqtk_trimfq Toolkit for processing sequences in FASTA/Q formats Data management Data handling Sequence file editing 437653
seqtk
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1.3.1 seqsero2 Salmonella serotype prediction from genome sequencing data Whole genome sequencing Sequence assembly Genomics Genome indexing Antimicrobial resistance prediction Genome alignment 13134
seqsero2
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1.3.2 seqprep Tool for merging paired-end Illumina reads and trimming adapters. Genomics Sequence assembly Sequencing Probes and primers Nucleic acid design 2742
seqprep
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2.10.1 seqkit_fx2tab seqkit_grep seqkit_head seqkit_locate seqkit_sort seqkit_stats seqkit_translate A cross-platform and ultrafast toolkit for FASTA/Q file manipulation Database management Sequence analysis DNA transcription Sequence trimming DNA translation Sequence conversion 10086
seqkit
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0.1.2 seqcomplexity Sequence complexity for raw reads 202
seqcomplexity
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2.3 seq2hla Precision HLA typing and expression from RNAseq data Transcriptomics Mapping Read mapping Genetic variation analysis 433
seq2hla
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2.1.0 semibin_bin semibin_concatenate_fasta semibin_generate_cannot_links semibin_generate_sequence_features semibin semibin_train SemiBin: Semi-supervised Metagenomic Binning Using Siamese Neural Networks Metagenomics Machine learning Microbial ecology Sequence assembly Sequence assembly Read binning 1914
semibin
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0.3.0 selenzy_wrapper Performs enzyme selection from a reaction query. 0
selenzy_wrapper
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1.3 seacr SEACR is intended to call peaks and enriched regions from sparse CUT&RUN or chromatin profiling data in which background is dominated by zeroes. 13318
seacr
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0.13.2 seaborn seaborn_pairgrid Seaborn is a Python data visualization library based on Matplotlib. 0
seaborn
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1.0.0+galaxy2 scpipe A flexible preprocessing pipeline for single-cell RNA-sequencing data Gene expression RNA-Seq Sequencing Genome annotation Validation Alignment Visualisation 1419
bioconductor-scpipe
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1.6.16 scoary Scoary calculates the assocations between all genes in the accessory genome and the traits. Genotype and phenotype Model organisms GWAS study Functional genomics Analysis 1120
scoary
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0.4.2 scikit_bio_diversity_beta_diversity scikit-bio: an open-source, BSD-licensed, python package providing data structures, algorithms, and educational resources for bioinformatics 2044
scikit-bio
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4 schicexplorer_schicadjustmatrix schicexplorer_schiccluster schicexplorer_schicclustercompartments schicexplorer_schicclusterminhash schicexplorer_schicclustersvl schicexplorer_schicconsensusmatrices schicexplorer_schiccorrectmatrices schicexplorer_schiccreatebulkmatrix schicexplorer_schicdemultiplex schicexplorer_schicinfo schicexplorer_schicmergematrixbins schicexplorer_schicmergetoscool schicexplorer_schicnormalize schicexplorer_schicplotclusterprofiles schicexplorer_schicplotconsensusmatrices schicexplorer_schicqualitycontrol scHiCExplorer: Set of programs to process, analyze and visualize scHi-C data. Workflows DNA Chromosome conformation capture ChIP-seq Epigenetics Validation Visualisation Standardisation and normalisation 1521
schicexplorer
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0.0.7 sceasy_convert Converter between difference single-cell formats Data handling 1998
r-sceasy
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1.22.0 scater_create_qcmetric_ready_sce scater_filter scater_plot_dist_scatter scater_plot_pca scater_plot_tsne Scater (Single-Cell Analysis Toolkit for gene Expression data in R) is acollection of tools for doing various analyses of single-cell RNA-seq geneexpression data, with a focus on quality control and visualization. RNA-Seq Quality affairs Molecular genetics Read pre-processing Sequencing quality control Sequence visualisation 2447
bioconductor-scater
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1.10.2 scanpy_cluster_reduce_dimension scanpy_filter scanpy_inspect scanpy_normalize scanpy_plot scanpy_remove_confounders Scanpy – Single-Cell Analysis in Python Gene expression Cell biology Genetics Single-cell sequencing Differential gene expression analysis Principal component visualisation Expression profile clustering 123392
scanpy
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0.1.13 sbml2sbol Convert SBML to SBOL format 0
sbml2sbol
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0.1 sarscov2summary sarscov2summary custom script 393
sarscov2summary
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1.0 sarscov2formatter sarscov2formatter custom script 574
sarscov2formatter
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0.2.2 sansa_annotate Sansa is a tool for structural variant annotation. 139
sansa
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0.1.26 samblaster samblaster marks duplicates and can output split and discordant alignments from SAM/BAM files DNA Sequencing Mapping Split read mapping 0
samblaster
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2.3 salsa A tool to scaffold long read assemblies with Hi-C Sequence assembly DNA binding sites Mapping Genome assembly De-novo assembly Scaffolding 1934
salsa2
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1.26.0 ruvseq Remove Unwanted Variation from RNA-Seq Data Gene expression RNA-seq Differential gene expression analysis 3737
bioconductor-ruvseq
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5.0.3 rseqc_FPKM_count rseqc_RNA_fragment_size rseqc_RPKM_saturation rseqc_bam2wig rseqc_bam_stat rseqc_clipping_profile rseqc_deletion_profile rseqc_geneBody_coverage rseqc_geneBody_coverage2 rseqc_infer_experiment rseqc_inner_distance rseqc_insertion_profile rseqc_junction_annotation rseqc_junction_saturation rseqc_mismatch_profile rseqc_read_GC rseqc_read_NVC rseqc_read_distribution rseqc_read_duplication rseqc_read_hexamer rseqc_read_quality rseqc_tin an RNA-seq quality control package Sequencing Data handling 415667
rseqc
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2.7.0 rrparser Reaction Rules Parser 0
rrparser
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5.13.1 rptools_rpextractsink rptools_rpfba rptools_rpranker rptools_rpreport rptools_rpviz Suite of tools that work on rpSBML format 0
rptools
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5.12.3 rpfba Perform FBA for the RetroPath2.0 heterologous pathways 0
rptools
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1.2.2 rpbasicdesign Extracting enzyme IDs from rpSBML files 0
rpbasicdesign
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1.5.1 rp2paths Enumerate and seperate the different pathways generated by RetroPath2.0 0
rp2paths
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3.2.1 rp2biosensor Build Sensing-Enabling Metabolic Pathways from RetroPath2.0 output 0
rp2biosensor
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3.13.0 roary Roary the pangenome pipeline DNA Genomics Mapping Genome assembly 38357
roary
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2.3.0 rna_quast rnaQuast (RNA Quality Assessment Tool) evaluates genome assemblies. Sequence assembly Transcriptomics RNA-Seq De-novo assembly Transcriptome assembly Sequence assembly validation 2416
rnaquast
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1.2.0 ribowaltz_process ribowaltz_plot Calculation of optimal P-site offsets, diagnostic analysis and visual inspection of ribosome profiling data Computational biology 194
ribowaltz
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2.7.11b rna_star rna_starsolo RNA STAR is an ultra fast universal RNA and scRNA-seq aligner and mapper RNA-Seq Transcriptomics Sequence alignment 1026347
star
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3.0.2 rgcca multi-block analysis 131
rgccacmd
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0.1.8 revoluzer_crex revoluzer_distmat revoluzer wrappers Molecular evolution Phylogeny Structural variation detection 3046
revoluzer
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1.0.2 resize_coordinate_window Contains a tool that modifies the start and stop coordinates of GFF data, expanding the coordinate windowby a specified size. 303
python
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1.4.2 cast melt Flexibly restructure and aggregate data using just the two functions melt and dcast 4179
r-reshape2
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repmatch_gff3 Contains a tool that matches corresponding peak-pair midpoints from separate datasets based onuser-defined criteria. 722
matplotlib
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2.0.5 repeatmodeler RepeatModeler - Model repetitive DNA Sequence composition, complexity and repeats Sequence composition, complexity and repeats Repeat sequence detection 19323
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4.1.5 repeatmasker_wrapper RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences. Sequence analysis Sequence composition, complexity and repeats Genome annotation 21398
repeatmasker
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red
2018.09.10 red Red (REpeat Detector) RNA Sequencing Data visualisation RNA-Seq analysis Editing 1927
red
red
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1.16.1 recentrifuge "With Recentrifuge, researchers can analyze results from taxonomic classifiers using interactive charts with emphasis on the confidence level of the classifications.In addition to contamination-subtracted samples.Recentrifuge provides shared and exclusive taxa per sample,thus enabling robust contamination removal and comparative analysis in environmental and clinical metagenomics." Metagenomics Microbial ecology Metagenomic sequencing Taxonomic classification Expression analysis Cross-assembly 2477
recentrifuge
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0.2.2 read_it_and_keep Rapid decontamination of SARS-CoV-2 sequencing reads Pathology Genomics Filtering Genome alignment 3785
read-it-and-keep
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1.0.3+galaxy1 rcorrector Rcorrector (RNA-seq error CORRECTOR) is a kmer-based error correction method for RNA-seq data. RNA RNA-Seq Sequencing Sequencing error detection 779
rcorrector
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8.2.12 raxml RAxML - A Maximum Likelihood based phylogenetic inference Phylogenetics Sequence analysis Sequence analysis Phylogenetic tree analysis 31039
raxml
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1.8.3 raven Raven is a de novo genome assembler for long uncorrected reads. Sequence assembly Whole genome sequencing Genomics De-novo assembly Genome assembly Read pre-processing 23502
raven-assembler
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2.0.0 rasusa Randomly subsample sequencing reads to a specified coverage Genomics Sequence analysis Sequence assembly Sequencing RNA-Seq Sequence assembly validation Sequencing quality control 71
rasusa
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2.3.2 rapidnj Galaxy wrapper for the RapidNJ tool Phylogeny Phylogenetic tree generation 5100
rapidnj
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2.1.0 ragtag Reference-guided scaffolding of draft genomes tool. Sequence assembly Genome assembly 6261
ragtag
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0.2.3 raceid_clustering raceid_filtnormconf raceid_inspectclusters raceid_inspecttrajectory raceid_trajectory RaceID3, StemID2, FateID - scRNA analysis Cell biology Molecular interactions, pathways and networks RNA-Seq Gene expression Expression profile clustering Expression analysis Molecular dynamics 9983
r-raceid
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2.5 quicktree neighbour-joining phylogenetic inference Phylogenetics Phylogenetic inference (from molecular sequences) 65
quicktree
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0.3 quickmerge Merge long-read and hybrid assemblies to increase contiguity Structural variation Sequence assembly DNA polymorphism Whole genome sequencing Genotype and phenotype Genome assembly Scaffolding De-novo assembly Genotyping 0
quickmerge
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3.3.1 filter_tabular query_tabular sqlite_to_tabular Loads tabular files into a SQLite DB to perform a SQL query producing a tabular output 168754
python
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0.9.0 query_impc Contains a tool to query the IMPC database. 4
requests
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5.3.0 quast Quast (Quality ASsessment Tool) evaluates genome assemblies. Sequence assembly Visualisation Sequence assembly validation 216176
quast
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2.3 qualimap_bamqc qualimap_counts qualimap_multi_bamqc qualimap_rnaseq Qualimap 2 is a platform-independent application written in Java andR that facilitates the quality control of alignment sequencing data and itsderivatives like feature counts. Data quality management Sequencing quality control 858426
qualimap
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0.1.0 qq_manhattan 16
r-qqman
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0.1.0 qiime_extract_viz Extract vizualization from QIIME artifacts 104
unzip
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qiime_align_seqs qiime_alpha_diversity qiime_alpha_rarefaction qiime_assign_taxonomy qiime_beta_diversity qiime_beta_diversity_through_plots qiime_compare_categories qiime_core_diversity qiime_count_seqs qiime_extract_barcodes qiime_filter_alignment qiime_filter_fasta qiime_filter_otus_from_otu_table qiime_filter_samples_from_otu_table qiime_filter_taxa_from_otu_table qiime_jackknifed_beta_diversity qiime_make_emperor qiime_make_otu_heatmap qiime_make_phylogeny qiime_multiple_join_paired_ends qiime_multiple_split_libraries_fastq qiime_pick_closed_reference_otus qiime_pick_open_reference_otus qiime_pick_otus qiime_pick_rep_set qiime_plot_taxa_summary qiime_split_libraries qiime_split_libraries_fastq qiime_summarize_taxa qiime_summarize_taxa_through_plots qiime_upgma_cluster qiime_validate_mapping_file QIIME to perform microbial community analysis Microbial ecology Phylogeny Metagenomics Metatranscriptomics Demultiplexing Visualisation Taxonomic classification Phylogenetic analysis Sequencing quality control 44433
qiime
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qiime_collapse_samples qiime_make_otu_table QIIME to perform microbial community analysis Microbial ecology Phylogeny Metagenomics Metatranscriptomics Demultiplexing Visualisation Taxonomic classification Phylogenetic analysis Sequencing quality control 2475
qiime
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1.0.0+galaxy1 qfilt Filter sequencing data 0
qfilt
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1.4.2 pysradb_search pysradb allows to retrieve metadata, such as run accession numbers, from SRA and ENA based on multiple criteria. Sequencing Gene transcripts Bioinformatics Deposition Data retrieval 175
pysradb
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3.8 pygenomeTracks pyGenomeTracks: Standalone program and library to plot beautiful genome browser tracks. Model organisms Imaging Workflows Visualisation Formatting 28461
pygenometracks
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5.0.2 pyega3 EGA python client uses the EGA REST API to download authorized datasets and files. 3123
pyega3
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2.5.2 pycoqc QC metrics for ONT Basecalling Sequence analysis Data quality management Sequencing Sequencing quality control Statistical calculation 27108
pycoqc
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1.2.6 purge_dups Purge haplotigs and overlaps in an assembly based on read depth Sequence assembly Genome assembly Read binning Scaffolding 22322
purge_dups
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1.0.4 pureclip PureCLIP is an HMM based peak caller specifically designed for eCLIP/iCLIP data 1559
pureclip
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1.0.3 psiclass PsiCLASS is a reference-based transcriptome assembler for single or multiple RNA-seq samples. Sequence assembly Transcriptome assembly 26
psiclass
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6.3.6 proteinortho proteinortho_clustering proteinortho_grab_proteins proteinortho_summary Proteinortho is a tool to detect orthologous proteins/genes within different species. Comparative genomics Sequence clustering Sequence analysis 4314
proteinortho
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0.1.6 prot_scriber Protein annotation of short human readable descriptions 12
prot-scriber
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1.14.6 prokka Rapid annotation of prokaryotic genomes Genomics Model organisms Virology Gene prediction Coding region prediction Genome annotation 1132458
prokka
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progressivemauve xmfa2gff3 Mauve/ProgressiveMauve Multiple Sequence Aligner 5725
progressivemauve
To update
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2.6.3 prodigal A protein-coding gene prediction software tool for bacterial and archaeal genomes Genomics Sequence analysis Genome annotation 4103
prodigal
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@TOOL_VERSION+galaxy2 prinseq PRINSEQ is a tool for easy and rapid quality control and data processing of metagenomic and metatranscriptomic datasets Transcriptomics Metagenomics Genomics Read pre-processing Sequence trimming Sequence contamination filtering 24136
prinseq
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0.0.7 pretext_graph pretext_map pretext_snapshot Process genome contacts maps processing images. 8653
pretextgraph
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0.6.2 presto_alignsets presto_assemblepairs presto_buildconsensus presto_collapseseq presto_filterseq presto_maskprimers presto_pairseq presto_parseheaders presto_parselog presto_partition prestor_abseq3 pRESTO toolkit for immune repertoire analysis. Sequencing DNA Immunology Nucleic acid sequence analysis 73477
presto
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UseGalaxy.or11
2.2.4 ppanggolin_all ppanggolin_msa ppanggolin_projection ppanggolin_rarefaction Microbial Partitioned PanGenome Metagenomics Gene and protein families Model organisms Public health and epidemiology Mapping Rarefaction Essential dynamics Sequence assembly Genome annotation 0
ppanggolin
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0.6.1a1 poretools_events poretools_extract poretools_hist poretools_nucdist poretools_occupancy poretools_qualdist poretools_qualpos poretools_squiggle poretools_stats poretools_tabular poretools_times poretools_winner poretools_yield_plot A flexible toolkit for exploring datasets generated by nanopore sequencing devices from MinION for the purposes of quality control and downstream analysis. DNA Sequencing Nucleic acid sequence analysis 73812
poretools
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porechop Porechop - Finding and removing adapters from Oxford Nanopore reads 483293
porechop
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0.6.1 polypolish "Polypolish is a tool for polishing genome assemblies with short reads.Polypolish uses SAM files where each read has been aligned to all possible locations (not just a single best location).This allows it to repair errors in repeat regions that other alignment-based polishers cannot fix." Sequence assembly Sequence composition, complexity and repeats Mapping Genome assembly Read mapping Mapping assembly Sequencing error detection 1242
polypolish
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1.90b6.21 plink Whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner. GWAS study Genetic variation analysis 1865
plink
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2.1.6 plasmidfinder "PlasmidFinder provides the detection of replicons in the WGSand assigns the plasmids under study to lineages that trace backthe information to the existing knowledge on Inc groups and suggestspossible reference plasmids for each lineage" Whole genome sequencing Sequence assembly Mapping Probes and primers Genome assembly Scaffolding Multilocus sequence typing 32622
plasmidfinder
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1.1.0 PlasFlow PlasFlow - Prediction of plasmid sequences in metagenomic contigs. Metagenomics Sequence assembly Mobile genetic elements Machine learning Sequence analysis 62172
plasflow
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0.1.1 plasclass PlasClass is a tool to classify sequences of plasmid or chromosomal origin Metagenomics Sequence assembly DNA Metagenomic sequencing Sequence classification Sequence assembly k-mer counting 0
plasclass
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0.37.3.1 pizzly Pizzly is a program for detecting gene fusions from RNA-Seq data of cancer samples. 1948
pizzly
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0.2 pipelign Multipe sequence alignment 10918
pipelign
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1.0.2 pimento_are_there_primers pimento_auto pimento_choose_primer_cutoff pimento_find_cutoffs pimento_gen_bcv pimento_std A PrIMEr infereNce TOolkit to facilitate large-scale calling of metabarcoding amplicon sequence variants. 0
mi-pimento
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1.20.1 pilon pilon is a tool for assembly improvement and variant analysis in bacteria Assembly Sequence assembly Analysis Read alignment 23352
pilon
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2.5.3 picrust2_add_descriptions picrust2_hsp picrust2_metagenome_pipeline picrust2_pathway_pipeline picrust2_pipeline picrust2_place_seqs picrust2_shuffle_predictions PICRUSt2: Phylogenetic Investigation of Communities by Reconstruction of Unobserved States Metagenomics Microbiology Phylogenetics Metagenomic sequencing Phylogenetic reconstruction Expression analysis Rarefaction Pathway analysis 5428
picrust2
To update
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1.1.1 picrust_categorize picrust_compare_biom picrust_format_tree_and_trait_table picrust_metagenome_contributions picrust_normalize_by_copy_number picrust_predict_metagenomes PICRUSt wrappers Metagenomics Microbial ecology Functional, regulatory and non-coding RNA Metagenomic sequencing Phylogenetic reconstruction Expression analysis Genome annotation DNA barcoding 3887
picrust
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0.2.0 pick_value Compose a text parameter value using text, integer and float values 9960
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3.1.1 picard_AddCommentsToBam picard_AddOrReplaceReadGroups picard_BedToIntervalList picard_CleanSam picard_CASM picard_CollectBaseDistributionByCycle picard_CollectGcBiasMetrics picard_CollectHsMetrics picard_CollectInsertSizeMetrics picard_CollectRnaSeqMetrics picard_artifact_metrics picard_CollectWgsMetrics picard_DownsampleSam picard_EstimateLibraryComplexity picard_FastqToSam picard_FilterSamReads picard_FixMateInformation picard_MarkDuplicates picard_MarkDuplicatesWithMateCigar picard_MeanQualityByCycle picard_MergeBamAlignment picard_MergeSamFiles picard_NormalizeFasta picard_QualityScoreDistribution picard_ReorderSam picard_ReplaceSamHeader picard_RevertOriginalBaseQualitiesAndAddMateCigar picard_RevertSam picard_SamToFastq picard_SortSam picard_ValidateSamFile Picard SAM/BAM manipulation tools. Sequencing Formatting 1143229
picard
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3.3.20220408 phyml PhyML is a phylogeny software based on the maximum-likelihood principle. Phylogenetics Bioinformatics Phylogenetics Phylogenetic tree generation (maximum likelihood and Bayesian methods) 3095
phyml
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1.50.0 phyloseq_add_rank_names phyloseq_from_biom phyloseq_from_dada2 phyloseq_plot_bar phyloseq_plot_ordination phyloseq_plot_richness phyloseq_tax_glom Handling and analysis of high-throughput microbiome census data Microbiology Sequence analysis Metagenomics Deposition Analysis Visualisation 2248
bioconductor-phyloseq
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1.3.2 pharokka rapid standardised annotation tool for bacteriophage genomes and metagenomes Metagenomics Sequence sites, features and motifs Workflows Functional, regulatory and non-coding RNA Genome annotation Antimicrobial resistance prediction tRNA gene prediction Formatting Sequence assembly 11358
pharokka
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1.2.0 pgx_freqplot pgx_loader pgxLoader and pgxFreqplot functions from pgxRpi 0
bioconductor-pgxrpi
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0.9.6 iuc_pear PEAR evaluates all possible paired-end read overlaps Sequence assembly Sequence merging 37315
pear
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1.0 peakzilla Peakzilla identifies sites of enrichment and transcription factor binding sites from ChIP-seq and ChIP-exo experiments. 40
python
To update
UseGalaxy.eu1
1.0.2 pe_histogram Contains a tool that produces an insert size histogram for a paired-end BAM file. 17759
openjdk
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25.07.0 pdfimages PDF image extractor. 0
poppler
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3.0.1+galaxy0 pcdl_get_anndata pcdl_get_cell_attribute pcdl_get_cell_attribute_list pcdl_get_cell_df pcdl_get_celltype_list pcdl_get_conc_attribute pcdl_get_conc_df pcdl_get_substrate_list pcdl_get_unit_dict pcdl_get_version pcdl_make_cell_vtk pcdl_make_conc_vtk pcdl_make_gif pcdl_make_graph_gml pcdl_make_movie pcdl_plot_contour pcdl_plot_scatter pcdl_plot_timeseries pcdl PhysiCell Data Loader. 0
To update
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3.5.0 bam2fastx Convert PacBio Bam File to fasta or fastq file 403
pbtk
Up-to-date
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1.17.0 pbmm2 A minimap2 SMRT wrapper for PacBio data. Mapping Pairwise sequence alignment Sorting 122
pbmm2
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2.0.2 pbgcpp Compute genomic consensus and call variants using PacBio reads mapped to a reference Mapping Variant calling 0
pbgcpp
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1.34.0 pathview Pathview is a tool set for pathway based data integration and visualization. Molecular interactions, pathways and networks Systems biology Data visualisation Pathway or network analysis Pathway or network visualisation 16877
bioconductor-pathview
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1.0.2 parse_mito_blast Filtering blast out from querying assembly against mitochondrial database. 1057
parse_mito_blast
Up-to-date
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4.3 pangolin Pangolin assigns SARS-CoV-2 genome sequences their most likely lineages under the Pango nomenclature system. Virology Tree-based sequence alignment Variant classification 19682
pangolin
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1.5.2 panaroo A Bacterial Pangenome Analysis Pipeline Workflows Sequence assembly Gene and protein families Plant biology Sequencing De-novo assembly Genome assembly Clustering 129
panaroo
Up-to-date
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1.1.3 pairtools_dedup pairtools_parse pairtools_sort pairtools_split pairtools_stats Flexible tools for Hi-C data processing 406
pairtools
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0.0.5 pacu_map pacu_snp PACU is a workflow for whole genome sequencing based phylogeny of Illumina and ONT R9/R10 data. Phylogenetics Sequence analysis Clustering 55
pacu_snp
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UseGalaxy.eu2
0.1 packaged_annotation_loader Tool to make cached genome annotation data available as a list of datasets collection 0
python
To update
2.5.5 orthofinder_onlygroups Accurate inference of orthologous gene groups made easy Phylogenetics Phylogenomics Bioinformatics Comparative genomics Sequence analysis Genome comparison Phylogenetic tree generation (from molecular sequences) Phylogenetic tree analysis Genome alignment 3759
orthofinder
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0.0.4 orfipy Galaxy wrapper for ORFIPY Computer science RNA-Seq Transcriptomics Small molecules Coding region prediction Database search Transcriptome assembly De-novo assembly 3285
orfipy
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1.3.5 optitype Precision HLA typing from NGS data 627
optitype
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v2.0.2 optdoe Optimal Design Of Experiment 0
doebase
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0.1.0+galaxy0 openalex_explorer Fetch citing papers from OpenAlex using DOI, ID and title 0
python
To update
UseGalaxy.eu1
1.45 onto_tk_get_ancestor_terms onto_tk_get_child_terms onto_tk_get_descendent_terms onto_tk_get_parent_terms onto_tk_get_parent_terms_by_relationship_type onto_tk_get_relationship_id_vs_relationship_def onto_tk_get_relationship_id_vs_relationship_name onto_tk_get_relationship_id_vs_relationship_namespace onto_tk_get_relationship_types onto_tk_get_root_terms onto_tk_get_subontology_from onto_tk_term_id_vs_term_def onto_tk_term_id_vs_term_name onto_tk_get_term_synonyms onto_tk_get_terms onto_tk_get_terms_by_relationship_type onto_tk_obo2owl onto_tk_obo2rdf onto_tk_term_id_vs_term_def ONTO-Toolkit is a collection of tools for managing ontologies. 665
perl-onto-perl
Up-to-date
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3.1.3 ont_fast5_api_compress_fast5 ont_fast5_api_fast5_subset ont_fast5_api_multi_to_single_fast5 ont_fast5_api_single_to_multi_fast5 ont_fast5_api is a simple interface to HDF5 files of the Oxford Nanopore FAST5 file format. 3090
ont-fast5-api
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0.3.1 omark Proteome quality assessment software Proteomics Sequence analysis Statistics and probability Sequence assembly validation Differential protein expression profiling 741
To update
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0.3 odgi_build odgi_viz Representing large genomic variation graphs with minimal memory overhead requires a careful encoding of the graph entities. odgi follows the dynamic GBWT in developing a byte-packed version of the graph and paths through it. 29
odgi
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0.1.2.6 ococo Variant detection of SNVs 3508
ococo
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1.2.13 obi_illumina_pairend obi_ngsfilter obi_annotate obi_clean obi_convert obi_grep obi_sort obi_stat obi_tab obi_uniq OBITools is a set of programs developed to simplify the manipulation of sequence files Sequence analysis DNA Sequencing Sequence analysis Sequence analysis 46515
obitools
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2.3.3 nugen_nudup Marks/removes PCR introduced duplicate molecules based on the molecular tagging technology used in NuGEN products. Sequencing Genomics Duplication detection Sequence analysis 0
nudup
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4.3.1 novoplasty NOVOPlasty is a de novo assembler and heteroplasmy/variance caller for short circular genomes. 12003
novoplasty
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3.5.5 nonpareil Estimate average coverage in metagenomic datasets Operation 305
nonpareil
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ngsutils_bam_filter NGSUtils is a suite of software tools for working with next-generation sequencing datasets.Starting in 2009, we (Liu Lab @ Indiana University School of Medicine) starting working withnext-generation sequencing data. We initially started doing custom coding for each project in a one-off manner.It quickly became apparent that this was an inefficient manner to work, so we started assembling smallerutilities that could be adapted into larger, more complicated, workflows. We have used them for Illumia,SOLiD, 454, Ion Torrent, and Pac Bio sequencing data. We have used them for DNA and RNA resequcing,ChIP-Seq, CLIP-Seq, and targeted resequencing (Agilent exome capture and PCR targeting).These tools are also used heavily in our in-house DNA and RNA mapping pipelines.NGSUtils is made up of 50+ programs, mainly written in Python.These are separated into modules based on the type of file that is to be analyzed. Genomics Transcriptomics Read pre-processing Sequencing quality control Variant calling Formatting Sequence contamination filtering 66759
ngsutils
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0.2.7 ngmlr CoNvex Gap-cost alignMents for Long Reads Sequencing Mapping DNA structural variation DNA mapping Sequence alignment Genetic variation analysis 1406
ngmlr
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2.7.0 nextalign nextclade Identify differences between your sequences and a reference sequence used by Nextstrain Genomics Sequence analysis Cladistics Methylation analysis Variant calling 18621
nextalign
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1.6+galaxy1 newick_display Perform operations on Newick trees Phylogeny Genomics Computer science Phylogenetic tree generation Phylogenetic tree analysis Phylogenetic tree reconstruction 64737
newick_utils
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0.0.1_update20200803 necat Error correction and de-novo assembly for ONT Nanopore reads Sequence assembly De-novo assembly 975
necat
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0.5.5 ncbi_fcs_gx FCS-GX detects contamination from foreign organisms in genome sequences using the genome cross-species aligner (GX). Sequence analysis Sequence assembly Sequence assembly validation Sequence trimming Sequence contamination filtering 6770
ncbi-fcs-gx
Up-to-date
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1.70 ncbi_eutils_ecitmatch ncbi_eutils_efetch ncbi_eutils_einfo ncbi_eutils_elink ncbi_eutils_epost ncbi_eutils_esearch ncbi_eutils_esummary NCBI Entrez E-Utilties allow fetching data from NCBI Databases 3235
python
To update
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22.4 ncbi_entrez_direct_efetch ncbi_entrez_direct_einfo ncbi_entrez_direct_esearch NCBI Entrez Direct allow fetching data from NCBI Databases 3
entrez-direct
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18.5.1 datasets_download_gene datasets_download_genome NCBI datasets downloads biological sequence data across all domains of life from NCBI. Biological databases Data handling Sequence database search Data retrieval 20804
ncbi-datasets-cli
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0.2.8 ncbi_acc_download Download sequences from GenBank/RefSeq by accession through the NCBI ENTREZ API 34900
ncbi-acc-download
Up-to-date
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0.6.11 nanopolishcomp_eventaligncollapse nanopolishcomp_freqmethcalculate NanopolishComp contains 2 modules. Eventalign_collapse collapses the raw file generated by nanopolish eventalign by kmers rather than by event. Freq_meth_calculate methylation frequency at genomic CpG sites from the output of nanopolish call-methylation. Sequence analysis Sequencing Genetic variation Methylation analysis Collapsing methods 1120
nanopolishcomp
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1.46.1 nanoplot Plotting tool for long read sequencing data and alignments Genomics Scatter plot plotting Box-Whisker plot plotting 193928
nanoplot
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1.0.0rc3.post2 nanocompore_db nanocompore_sampcomp Nanocompore compares 2 ONT nanopore direct RNA sequencing datasets from different experimental conditions expected to have a significant impact on RNA modifications. It is recommended to have at least 2 replicates per condition. For example one can use a control condition with a significantly reduced number of modifications such as a cell line for which a modification writing enzyme was knocked-down or knocked-out. Alternatively, on a smaller scale transcripts of interests could be synthesized in-vitro. Functional, regulatory and non-coding RNA RNA-Seq Gene transcripts Transcriptomics Transcription factors and regulatory sites Post-translation modification site prediction PolyA signal detection Genotyping k-mer counting 1150
nanocompore
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1.25.3 nanocomp Compare multiple runs of long read sequencing data and alignments Nucleic acids Bioinformatics Box-Whisker plot plotting Visualisation Multiple sample visualisation 0
nanocomp
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0.1.2 bicodon_counts_from_fasta codon_freq_from_bicodons find_nested_alt_orfs nAlt-ORFs: Nested Alternate Open Reading Frames (nAltORFs) 228
naltorfs
Up-to-date
UseGalaxy.or3
3.9.0 mzmine_batch mass-spectrometry data processing, with the main focus on LC-MS data Proteomics Metabolomics Proteomics experiment Small molecules Natural product identification Standardisation and normalisation Peptide database search Deisotoping Clustering Filtering Chromatographic alignment Peak detection Peptide identification Chromatogram visualisation Mass spectrum visualisation Structure visualisation Plotting Heat map generation 11
mzmine
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UseGalaxy.eu1
0.10.0 mykrobe_predict Antibiotic resistance predictions Whole genome sequencing Genotype and phenotype Probes and primers Genetic variation Metagenomics Antimicrobial resistance prediction Variant calling Genotyping Sequence trimming 0
mykrobe
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0.1.6 cluster_analyze_embed_muon mudata_import_export plot_muon preprocess_muon muon is a Python framework for multimodal omics analysis Cell biology Single-cell sequencing Gene expression Epigenetics Multiomics 0
muon
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4.0.0 mummer_delta_filter mummer_dnadiff mummer_mummer mummer_mummerplot mummer_nucmer mummer_show_coords Mummer4 Tools Sequence analysis Human genetics Multiple sequence alignment 65097
mummer4
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1.27 multiqc MultiQC aggregates results from bioinformatics analyses across many samples into a single report Sequencing Bioinformatics Sequence analysis Genomics Validation Sequencing quality control 498453
multiqc
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1.12.0 multigsea GSEA-based pathway enrichment analysis for multi-omics data Metabolomics Molecular interactions, pathways and networks Proteomics Transcriptomics Small molecules Gene-set enrichment analysis Aggregation Pathway analysis 159
bioconductor-multigsea
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0.74.0 multigps Analyzes collections of multi-condition ChIP-seq data. 886
fonts-conda-ecosystem
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0.1.2 msaboot A multiple sequences alignment bootstrapping tool. 2169
msaboot
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1.0 mothur_align_check mothur_align_seqs mothur_amova mothur_anosim mothur_bin_seqs mothur_biom_info mothur_chimera_bellerophon mothur_chimera_ccode mothur_chimera_check mothur_chimera_perseus mothur_chimera_pintail mothur_chimera_slayer mothur_chimera_uchime mothur_chimera_vsearch mothur_chop_seqs mothur_classify_otu mothur_classify_seqs mothur_classify_tree mothur_clearcut mothur_cluster_classic mothur_cluster_fragments mothur_cluster_split mothur_cluster mothur_collect_shared mothur_collect_single mothur_consensus_seqs mothur_cooccurrence mothur_corr_axes mothur_count_groups mothur_count_seqs mothur_create_database mothur_degap_seqs mothur_deunique_seqs mothur_deunique_tree mothur_dist_seqs mothur_dist_shared mothur_fastq_info mothur_filter_seqs mothur_filter_shared mothur_get_communitytype mothur_get_coremicrobiome mothur_get_dists mothur_get_group mothur_get_groups mothur_get_label mothur_get_lineage mothur_get_mimarkspackage mothur_get_otulabels mothur_get_otulist mothur_get_oturep mothur_get_otus mothur_get_rabund mothur_get_relabund mothur_get_sabund mothur_get_seqs mothur_get_sharedseqs mothur_heatmap_bin mothur_heatmap_sim mothur_homova mothur_indicator mothur_lefse mothur_libshuff mothur_list_otulabels mothur_list_seqs mothur_make_biom mothur_make_contigs mothur_make_design mothur_make_fastq mothur_make_group mothur_make_lefse mothur_make_lookup mothur_make_shared mothur_make_sra mothur_mantel mothur_merge_count mothur_merge_files mothur_merge_groups mothur_merge_sfffiles mothur_merge_taxsummary mothur_metastats mothur_mimarks_attributes mothur_nmds mothur_normalize_shared mothur_otu_association mothur_otu_hierarchy mothur_pairwise_seqs mothur_parse_list mothur_parsimony mothur_pca mothur_pcoa mothur_pcr_seqs mothur_phylo_diversity mothur_phylotype mothur_pre_cluster mothur_primer_design mothur_rarefaction_shared mothur_rarefaction_single mothur_remove_dists mothur_remove_groups mothur_remove_lineage mothur_remove_otulabels mothur_remove_otus mothur_remove_rare mothur_remove_seqs mothur_rename_seqs mothur_reverse_seqs mothur_screen_seqs mothur_sens_spec mothur_seq_error mothur_sffinfo mothur_shhh_flows mothur_shhh_seqs mothur_sort_seqs mothur_split_abund mothur_split_groups mothur_sub_sample mothur_summary_qual mothur_summary_seqs mothur_summary_shared mothur_summary_single mothur_summary_tax mothur_taxonomy_to_krona mothur_tree_shared mothur_trim_flows mothur_trim_seqs mothur_unifrac_unweighted mothur_unifrac_weighted mothur_unique_seqs mothur_venn Mothur wrappers Microbial ecology Taxonomy Sequence analysis Phylogeny DNA barcoding Sequencing quality control Sequence clustering Taxonomic classification Visualisation Sequence read processing Phylogenetic analysis 1262671
mothur
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0.3.11 mosdepth fast and flexible BAM/CRAM depth calculation 21679
mosdepth
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1.3.4.6 moabs MOABS for differential methylation analysis on Bisulfite sequencing data. 349
moabs
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1.16.0 mmuphin MMUPHin is an R package implementing meta-analysis methods for microbial community profiles 0
bioconductor-mmuphin
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17-b804f mmseqs2_easy_linclust_clustering mmseqs2_taxonomy_assignment MMseqs2 is an ultra fast and sensitive sequence search and clustering suite Metagenomics Sequence analysis Proteins Nucleic acids Gene and protein families Taxonomy Sequence similarity search Sequence alignment Sequence clustering Taxonomic classification 0
mmseqs2
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2.22.0 mlst mlst_list Scan contig files against PubMLST typing schemes Immunoproteins and antigens Multilocus sequence typing 42341
mlst
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1.1.7 mitos mitos2 de-novo annotation of metazoan mitochondrial genomes Zoology Whole genome sequencing Genome annotation 322857
mitos
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1.9.1 mitobim assemble mitochondrial genomes 1687
mitobim
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1.1 mirnature Computational detection of canonical microRNAs 22
mirnature
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0.3.0.1 mirmachine Tool to detect miRNA in genome sequences 7
mirmachine
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0.18 miniprot miniprot_index Align a protein sequence against a genome with affine gap penalty, splicing and frameshift. Sequence sites, features and motifs Sequence analysis Sequence alignment Protein sequence analysis 5362
miniprot
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2.28 minimap2 A fast pairwise aligner for genomic and spliced nucleotide sequences Mapping Pairwise sequence alignment 555047
minimap2
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0.3_r179 miniasm Miniasm - Ultrafast de novo assembly for long noisy reads (though having no consensus step) Genomics Sequence assembly De-novo assembly 24708
miniasm
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3.2.6 minia Short-read assembler based on a de Bruijn graph Sequence assembly Genome assembly 7460
minia
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1.0.3 migmap mapper for full-length T- and B-cell repertoire sequencing Immunoproteins, genes and antigens Sequence analysis Sequence analysis Read mapping 2684
migmap
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1.3.3 microsatbed Select microsatellites for a bed file 1617
python
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1.0.2 micro_decon An R package for removing contamination from metabarcoding (e.g., microbiome) datasets post-sequencing 0
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0.10.4 mg_toolkit_bulk_download mg_toolkit_original_metadata Metagenomics toolkit enables scientists to download all of the sample metadata for a given study or sequence to a single csv file. Metagenomics Data retrieval 13
mg-toolkit
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1.3.0 metawrapmg_binning A flexible pipeline for genome-resolved metagenomic data analysis Whole genome sequencing Metagenomic sequencing Metagenomics Read binning Sequence assembly Genome annotation Sequence trimming Demultiplexing 922
metawrap-mg
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0.1.5 metasbt_index metasbt_profile Microbial genomes characterization with Sequence Bloom Trees 0
sed
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4.1.1 customize_metaphlan_database extract_metaphlan_database merge_metaphlan_tables metaphlan MetaPhlAn for Metagenomic Phylogenetic Analysis Metagenomics Phylogenomics Taxonomic classification Taxonomic classification 37088
metaphlan
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1.16.0-0.0.1 metagenomeseq_normalizaton metagenomeSeq Normalization Metagenomics Sequencing Sequence visualisation Statistical calculation 1288
bioconductor-metagenomeseq
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7.bba0d80 metaeuk_easy_predict MetaEuk is a modular toolkit designed for large-scale gene discovery andannotation in eukaryotic metagenomic contigs. Metaeuk combines the fast andsensitive homology search capabilities of MMseqs2 with a dynamic programmingprocedure to recover optimal exons sets. It reduces redundancies in multiplediscoveries of the same gene and resolves conflicting gene predictions onthe same strand. Metagenomics Gene and protein families Homology-based gene prediction 496
metaeuk
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1.0.5 metabuli_classify Classifying metagenomes by jointly analysing both DNA and amino acid (AA) sequences Taxonomy Taxonomic classification 0
metabuli
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2.17 metabat2_jgi_summarize_bam_contig_depths metabat2 MetaBAT2 (Metagenome Binning based on Abundance and Tetranucleotide frequency) is an automated metagenome binningsoftware that integrates empirical probabilistic distances of genome abundance and tetranucleotide frequency. Metagenomics Sequence assembly Metagenomic sequencing Read binning Sequence assembly Genome annotation 12254
metabat2
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1.3 meryl_arithmetic_kmers meryl_count_kmers meryl_filter_kmers meryl_groups_kmers meryl_histogram_kmers meryl_print meryl_trio_mode Meryl a k-mer counter. Whole genome sequencing Genomics Sequence analysis Sequencing k-mer counting 211
merqury
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1.1.1 merquryfk_asmplot merquryfk_cnplot merquryfk_hapmaker merquryfk_happlot merquryfk_merquryfk FastK based version of Merqury 0
merquryfk
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1.3 merqury merquryplot Merqury is a tool for evaluating genomes assemblies based of k-mer operations. Sequence assembly Whole genome sequencing Plant biology Genome assembly k-mer counting Scaffolding Phasing De-novo assembly 6560
merqury
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1.1.2 merlin Pedigree Analysis package GWAS study Mapping Haplotype mapping Genetic mapping 0
merlin
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0.8.5 meningotype Assign sequence type to N. meningitidis genome assemblies Microbiology Genotype and phenotype Genotyping Multilocus sequence typing 0
meningotype
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4.11.2 meme_chip Performs motif discovery, motif enrichment analysis and clustering on large nucleotide datasets. 15133
graphicsmagick
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5.5.8 meme_dreme meme_fimo meme_meme meme_psp_gen meme_streme The MEME Suite allows the biologist to discover novel motifs in collections of unaligned nucleotideor protein sequences, and to perform a wide variety of other motif-based analyses. Sequence sites, features and motifs ChIP-seq RNA immunoprecipitation Epigenetics Small molecules Sequence motif discovery Sequence motif recognition Sequence motif comparison Transcriptional regulatory element prediction 50605
meme
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6.21.7 megan_blast2lca megan_blast2rma megan_daa2info megan_daa2rma megan_daa_meganizer megan_read_extractor megan_sam2rma MEGAN Community Edition - Interactive exploration and analysis of large-scale microbiome sequencing data. MEGAN is a tool for studying the taxonomic content of a set of DNA reads, typically collected in a metagenomics project.In a preprocessing step, a sequence alignment of all reads against a suitable database of reference DNA or proteinsequences must be performed to produce an input file for the program. MEGAN is suitable for DNA reads (metagenomedata), RNA reads (metatranscriptome data), peptide sequences (metaproteomics data) and, using a suitable synonymsfile that maps SILVA ids to taxon ids, for 16S rRNA data (amplicon sequencing). Sequence analysis Sequence analysis Taxonomic classification 4619
megan
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1.1.3 megahit_contig2fastg A subprogram within the Megahit toolkit for converting contigs to assembly graphs (fastg) Metagenomics Sequencing Ecology Sequence assembly Genome assembly 927
megahit
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1.2.9 megahit An ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph. Metagenomics Sequencing Ecology Sequence assembly Genome assembly 44056
megahit
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1.7.2 medaka_consensus medaka_consensus_pipeline medaka_snp medaka_variant Sequence correction provided by ONT Research Sequence assembly Machine learning Base-calling Variant calling Sequence assembly 199240
medaka
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mcl
22.282 mcl The Markov Cluster Algorithm, a cluster algorithm for graphs Molecular interactions, pathways and networks Clustering Network analysis Gene regulatory network analysis 153
mcl
mcl
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maxbin2 clusters metagenomic contigs into bins Metagenomics Sequence assembly Microbiology Sequence assembly 7691
maxbin2
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1.49.3 masigpro Identify significantly differential expression profiles in time-course microarray experiments Gene expression Molecular genetics Microarray experiment RNA-Seq Regression analysis 1186
coreutils
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3.1.3 mashmap Fast local alignment boundaries 2291
mashmap
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2.3 mash_screen mash_sketch Fast genome and metagenome distance estimation using MinHash Genomics Metagenomics Statistics and probability Sequence analysis DNA mutation Sequence distance matrix generation 12505
mash
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2.1.1b mapseq fast and accurate sequence read classification tool designed to assign taxonomy and OTU classifications to ribosomal RNA sequences. Functional, regulatory and non-coding RNA Sequence analysis Sequence sites, features and motifs k-mer counting 9229
perl
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1.0.0 maplot Generate MA plots for visualizing data distributions using Plotly or Matplotlib. 0
plotly
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0.2.0 map_param_value Map a parameter value to another value 7042
To update
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2.2.3 map_damage Tracks and quantifies specific ancient DNA damage patterns for authentication. DNA Sequencing Sequencing quality control Statistical calculation 0
mapdamage2
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0.5.3 malt_run Aligns an input sequence (DNA or proteins) against an index representing a collection of reference DNA or protein sequences. 25
malt
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2.31.11 maker maker_map_ids MAKER is a portable and easily configurable genome annotation pipeline.Its purpose is to allow smaller eukaryotic and prokaryotic genome projects to independently annotate their genomes and to create genome databases. Genomics DNA Sequence analysis Genome annotation 21746
maker
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0.5.9.2 mageck_count mageck_gsea mageck_mle mageck_pathway mageck_test Model-based Analysis of Genome-wide CRISPR-Cas9 Knockout (MAGeCK) is a computational tool to identifyimportant genes from the recent genome-scale CRISPR-Cas9 knockout screens technology. Genetics Genetic variation Genomics Genetic variation analysis 28661
mageck
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1.0.2+galaxy0 maf_stats1 MAF Coverage statistics 2501
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2.2.9.1 macs2_bdgbroadcall macs2_bdgcmp macs2_bdgdiff macs2_bdgpeakcall macs2_callpeak macs2_filterdup macs2_predictd macs2_randsample macs2_refinepeak MACS - Model-based Analysis of ChIP-Seq ChIP-seq Molecular interactions, pathways and networks Transcription factors and regulatory sites Peak calling Enrichment analysis Gene regulatory network analysis 365381
macs2
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1.18.0 maaslin2 MaAsLin2 is comprehensive R package for efficiently determining multivariable association between microbial meta'omic features and clinical metadata. Metagenomics Statistics and probability Filtering Statistical calculation Standardisation and normalisation Visualisation 3109
bioconductor-maaslin2
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2.1.0 m6anet m6anet to detect m6A RNA modifications from nanopore data RNA-Seq Transcriptomics RNA Machine learning Quantification Imputation Gene expression profiling 44
m6anet
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0.3.1 lumpy_prep lumpy_sv LUMPY - a general probabilistic framework for structural variant discovery 2121
lumpy-sv
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20 lorikeet_spoligotype Tools for M. tuberculosis DNA fingerprinting (spoligotyping) Genotype and phenotype Sequence analysis Genotyping 903
lorikeet
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2.1.5 lofreq_alnqual lofreq_call lofreq_filter lofreq_indelqual lofreq_viterbi LoFreq is a fast and sensitive variant-caller for inferring SNVs and indelsfrom next-generation sequencing data. It makes full use of base-call qualitiesand other sources of errors inherent in sequencing (e.g. mapping or base/indelalignment uncertainty), which are usually ignored by other methods or onlyused for filtering. 4855707
lofreq
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2.0.1 links Scaffold genome assemblies with long reads. Sequence assembly Mapping Sequencing Scaffolding Genome assembly Read mapping Read pre-processing Sequence trimming 1225
links
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1.6.0 lineagespot Identification of SARS-CoV-2 related metagenomic mutations based on a single (or a list of) variant(s) file(s) Metagenomics Gene transcripts Evolutionary biology Sequencing Genetic variation Variant calling 39
r-base
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3.58.1 limma_voom Perform RNA-Seq differential expression analysis using limma voom pipeline Molecular biology Genetics RNA-Seq analysis 92039
bioconductor-limma
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0.1.2 length_and_gc_content Gets gene length and gc content from a fasta and a GTF file 7657
r-optparse
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0.5.1 legsta Performs in silico Legionella pneumophila sequence based typing. Public health and epidemiology Sequence analysis 103
legsta
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1.0.2 lcrgenie Ligase Chain Reaction Genie 0
lcr_genie
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1.04.22 lastz_wrapper_2 lastz_d_wrapper Galaxy wrappers for the Lastz and Lastz_d Genomics Sequence alignment Read mapping 325060
lastz
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1205 last_al last_db last_split last_train last_maf_convert LAST finds similar regions between sequences. Genomics Comparative genomics Sequence alignment 383
last
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1.0.1 krocus Predict MLST directly from uncorrected long reads Public health and epidemiology Multilocus sequence typing k-mer counting 0
krocus
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1.2.1 krakentools_alpha_diversity krakentools_beta_diversity krakentools_combine_kreports krakentools_extract_kraken_reads krakentools_kreport2krona krakentools_kreport2mpa KrakenTools is a suite of scripts to be used alongside the Kraken Taxonomy Metagenomics Visualisation Aggregation 139895
krakentools
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0.0.3 kraken_taxonomy_report Kraken taxonomy report Metagenomics Taxonomy Visualisation Classification 11014
biopython
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1.2.0 kraken_biom Create BIOM-format tables (http://biom-format.org) from Kraken output (http://ccb.jhu.edu/software/kraken/) Metagenomics Taxonomy Genome annotation Taxonomic classification 4437
kraken-biom
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1.3.0 kofamscan Gene function annotation tool based on KEGG Orthology and hidden Markov model Genomics Structure analysis Sequence analysis Gene functional annotation 1646
kofamscan
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1.0.1 kmer2stats A tool for creating data files for statistics based on kmers 0
kmer2stats
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kma
1.5.1 kma_map Map with KMA 1
kma
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2.3.2 kleborate Screen genome assemblies of Klebsiella pneumoniae and the Klebsiella pneumoniae species complex (KpSC) Public health and epidemiology Metagenomics Population genomics Sequence assembly Whole genome sequencing Multilocus sequence typing Genome assembly Virulence prediction 650
kleborate
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2.2.7 king Kinship-based INference for Gwas 8
king
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3.0.0a3 khmer_abundance_distribution_single khmer_abundance_distribution khmer_count_median khmer_partition khmer_extract_partitions khmer_filter_abundance khmer_filter_below_abundance_cutoff khmer_normalize_by_median In-memory nucleotide sequence k-mer counting, filtering, graph traversal and more Sequence assembly Standardisation and normalisation De-novo assembly 5499
khmer
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1.0.2 kc-align Kc-Align custom tool Mapping Multiple sequence alignment 8688
kcalign
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0.48.0 kallisto_pseudo kallisto_quant kallisto is a program for quantifying abundances of transcripts from RNA-Seqdata, or more generally of target sequences using high-throughput sequencingreads. It is based on the novel idea of pseudoalignment for rapidlydetermining the compatibility of reads with targets, without the need foralignment. Transcriptomics RNA-Seq Gene expression Gene expression profiling 124410
kallisto
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1.10.1 kaiju_addtaxonnames kaiju_mergeoutputs kaiju_kaiju kaiju_kaiju2krona kaiju_kaiju2table taxonomic classification of high-throughput sequencing reads Metagenomics Taxonomic classification 0
kaiju
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20201223 jvarkit_wgscoverageplotter Jvarkit : Java utilities for Bioinformatics 21926
jvarkit-wgscoverageplotter
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jq
1.0 jq JQ is a lightweight and flexible command-line JSON processor 3059
jq
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1.0 join_files_by_id This tool will join datasets according to a column with identifier 0
r-data.table
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jellyfish Jellyfish is a tool for fast, memory-efficient counting of k-mers in DNA Sequence analysis Genomics k-mer counting 4689
kmer-jellyfish
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0.8.4 jcvi_gff_stats Compute statistics from a genome annotation in GFF3 format (using JCVI Python utilities) 7543
jcvi
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1.16.11 jbrowse_to_standalone jbrowse JBrowse Genome Browser integrated as a Galaxy Tool Genomics Genome visualisation 64507
jbrowse
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1.0.11 jasminesv Merge structural variants across samples 94
jasminesv
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1.0.0 iwtomics_loadandplot iwtomics_plotwithscale iwtomics_testandplot Interval-Wise Testing for Omics Data Statistics and probability Differential gene expression analysis Differentially-methylated region identification Peak calling Genome annotation Comparison 1396
bioconductor-iwtomics
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1.4.4 ivar_consensus ivar_filtervariants ivar_removereads ivar_trim ivar_variants iVar is a computational package that contains functions broadly useful for viral amplicon-based sequencing Virology Primer removal 1508647
ivar
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1.20.0 isoformswitchanalyzer Statistical identification of isoform switching from RNA-seq derived quantification of novel and/or annotated full-length isoforms. Computational biology Gene transcripts Sequence comparison Sequence analysis 4323
bioconductor-isoformswitchanalyzer
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1.7.3 isescan "ISEScan is a pipeline to identify IS (Insertion Sequence) elements in genome and metagenomebased on profile hidden Markov models constructed from manually curated IS elements." Genomics DNA structural variation Sequence analysis Genetic variation Structural variation detection 69744
isescan
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1.2.0 irma Iterative Refinement Meta-Assembler (IRMA) is a tool to construct assembly of highly variable RNA viruses. Mapping assembly 7548
irma
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1.0.5 irissv Refine insertion sequences 29
samtools
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2.4.0 iqtree Efficient phylogenomic software by maximum likelihood Phylogenetics Phylogenetic analysis Sequence analysis 79001
iqtree
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0.1.0+galaxy0 ipfp_norm Normalisation algorithm used to adjust matrices iteratively to satisfy specific row and column sum constraints while preserving the data structure. 0
numpy
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0.6.5 intervene_pairwise intervene_upset Create pairwise and upset plots Computational biology Sequence comparison Sequence visualisation 6418
intervene
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1.0.1+galaxy1 Interval2Maf1 Extract MAF blocks given a set of intervals Sequence analysis 19740
bx-python
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5.59-91.0 interproscan Interproscan queries the interpro database and provides annotations. Gene and protein families Sequence analysis Sequence motif recognition Protein feature detection 84530
interproscan
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0.0.1 galaxy_intermine_exchange InterMine Exporter 263
coreutils
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2.0.5 integron_finder "IntegronFinder identify integrons with high accuracy and sensitivity.It searches for attC sites using covariance models, for integron-integrases using HMM profiles, and for other features (promoters, attI site) using pattern matching" Functional genomics Mobile genetic elements Molecular biology Sequence analysis Nucleic acid feature detection Sequence motif recognition Protein feature detection Genome annotation 72347
integron_finder
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1.5.3 instrain_compare instrain_profile InStrain is a tool for analysis of co-occurring genome populations from metagenomes Mapping Metagenomics SNP detection Genome comparison 106
instrain
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1.22.0 infercnv Infer Copy Number Variation from Single-Cell RNA-Seq Data Heat map generation Expression analysis RNA-Seq analysis Copy number variation detection Clustering 29
bioconductor-infercnv
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2.15.2 iedb_api Get epitope binding predictions from IEDB-API 1590
python
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0.45 idr_download_by_ids Image Data Resource downloading tool 639
omero-py
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idr
2.0.3 idr Galaxy wrappers for the IDR package from Nathan Boleu 4931
idr
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idba_hybrid idba_tran idba_ud Wrappers for the idba assembler variants. Sequence assembly Sequence assembly 2938
idba
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1.3.3 icescreen identification of ICEs and IMEs in Bacillota genomes. Mobile genetic elements Sequence sites, features and motifs Genomics Molecular interactions, pathways and networks Structural variation Database search Protein feature detection 0
icescreen
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1.0.3 hypo Super Fast & Accurate Polisher for Long Read Genome Assemblies Sequence assembly Genomics Optimisation and refinement Genome assembly 505
hypo
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2.5.47 hyphy_absrel hyphy_annotate hyphy_bgm hyphy_busted hyphy_cfel hyphy_conv hyphy_fade hyphy_fel hyphy_fubar hyphy_gard hyphy_meme hyphy_prime hyphy_relax hyphy_slac hyphy_sm19 hyphy_strike_ambigs hyphy_summary Hypothesis Testing using Phylogenies Phylogeny Small molecules Molecular interactions, pathways and networks Statistical calculation 20949
hyphy
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2.1.6 hybpiper Analyse targeted sequence capture data Phylogenetics Plant biology Gene transcripts Sequence assembly Phylogenomics Sequence trimming Sequence assembly Read mapping 1778
hybpiper
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3.9 humann humann_barplot humann_join_tables humann_reduce_table humann_regroup_table humann_rename_table humann_renorm_table humann_split_stratified_table humann_split_table humann_unpack_pathways HUMAnN for functionally profiling metagenomes and metatranscriptomes at species-level resolution Metagenomics Phylogenomics Species frequency estimation Taxonomic classification Phylogenetic analysis 36509
humann
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2.0.9 htseq_count Count aligned reads (SAM/BAM) that overlap genomic features (GFF) Sequence analysis Nucleic acid sequence analysis 587449
htseq
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4.11 homer_annotatePeaks homer_findMotifs homer_findMotifsGenome homer_gtf_to_annotations homer_scanMotifGenomeWide HOMER (Hypergeometric Optimization of Motif EnRichment) is a suite of tools for Motif Discovery and next-gen sequencing analysis. Sequence motif discovery 10287
homer
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3.4 hmmer_alimask hmmer_hmmalign hmmer_hmmbuild hmmer_hmmconvert hmmer_hmmemit hmmer_hmmfetch hmmer_hmmscan hmmer_hmmsearch hmmer_jackhmmer hmmer_nhmmer hmmer_nhmmscan hmmer_phmmer HMMER is used for searching sequence databases for homologs of proteinsequences, and for making protein sequence alignments. It implementsmethods using probabilistic models called profile hidden Markov models(profile HMMs). Sequence analysis Sequence sites, features and motifs Gene and protein families Formatting Multiple sequence alignment Sequence profile generation Format validation Conversion Sequence generation Data retrieval Statistical calculation Database search Formatting Database search Database search Probabilistic sequence generation Statistical calculation Statistical calculation Sequence database search Formatting Sequence database search Database search Sequence database search 43031
hmmer
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1.3.1 hivclustering Infers transmission networks from pairwise distances inferred by tn93 0
python-hivclustering
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2.2.1 hisat2 HISAT2 is a fast and sensitive spliced alignment program. RNA-seq Sequence alignment 1504469
hisat2
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0.3.1 hifiasm_meta A hifiasm fork for metagenome assembly using Hifi reads. Sequence assembly Metagenomics Sequence assembly 457
hifiasm_meta
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0.25.0 hifiasm A fast haplotype-resolved de novo assembler 6697
hifiasm
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3.2.4 hicstuff_pipeline A toolkit to generate and manipulate Hi-C matrices 0
hicstuff
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3.7.6 hicexplorer_chicaggregatestatistic hicexplorer_chicdifferentialtest hicexplorer_chicexportdata hicexplorer_chicplotviewpoint hicexplorer_chicqualitycontrol hicexplorer_chicsignificantinteractions hicexplorer_chicviewpoint hicexplorer_chicviewpointbackgroundmodel hicexplorer_hicadjustmatrix hicexplorer_hicaggregatecontacts hicexplorer_hicaverageregions hicexplorer_hicbuildmatrix hicexplorer_hicbuildmatrixmicroc hicexplorer_hiccomparematrices hicexplorer_hiccompartmentspolarization hicexplorer_hicconvertformat hicexplorer_hiccorrectmatrix hicexplorer_hiccorrelate hicexplorer_hicdetectloops hicexplorer_hicdifferentialtad hicexplorer_hicfindrestrictionsites hicexplorer_hicfindtads hicexplorer_hichyperoptDetectLoops hicexplorer_hicinfo hicexplorer_hicinterintratad hicexplorer_hicmergedomains hicexplorer_hicmergeloops hicexplorer_hicmergematrixbins hicexplorer_hicnormalize hicexplorer_hicpca hicexplorer_hicplotaverageregions hicexplorer_hicplotdistvscounts hicexplorer_hicplotmatrix hicexplorer_hicplotsvl hicexplorer_hicplotviewpoint hicexplorer_hicquickqc hicexplorer_hicsummatrices hicexplorer_hictransform hicexplorer_hicvalidatelocations HiCExplorer: Set of programs to process, analyze and visualize Hi-C data. 75887
hicexplorer
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0.1.0 hgvsparser Parsing and building variant descriptor strings compliant with the HGVS standard 6353
r-base
To update
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1.0 heinz_bum heinz heinz_scoring heinz_visualization An algorithm for identification of the optimal scoring subnetwork. Genetics Gene expression Molecular interactions, pathways and networks Pathway or network analysis 3831
bioconductor-bionet
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3.2.0 ggplot2_heatmap2 heatmap.2 function from the R gplots package 143397
r-gplots
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0.3.14 som.py A tool to perform comparisons only based on chromosome, position, and allele identity for comparison of somatic callsets. Genomics DNA polymorphism Variant calling Sequence analysis Genotyping 0
hap.py
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1.3.8 hapog Hapo-G - Haplotype-Aware Polishing of Genomes Sequence assembly Genomics Genome assembly Optimisation and refinement 1003
hapog
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1.3.4 hapcut2 Robust and accurate haplotype assembly for diverse sequencing technologies Haplotype mapping Variant classification 123
hapcut2
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2.6.1 bio_hansel Heidelberg and Enteritidis SNP Elucidation Whole genome sequencing DNA polymorphism Genotype and phenotype Infectious disease Agricultural science Genotyping SNP detection Genome assembly 737
bio_hansel
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1.1.4 hamronize_summarize hamronize_tool Convert AMR gene detection tool output to hAMRonization specification format. Public health and epidemiology Microbiology Bioinformatics Data handling Antimicrobial resistance prediction Parsing 9491
hamronization
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0.1.0 halfdeep HalfDeep: Automated detection of intervals covered at half depth by sequenced reads. 48
halfdeep
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0.1.0 gwastools_manhattan_plot GWAS study Deposition Analysis Annotation 21
bioconductor-gwastools
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0.1 gvcftools_extract_variants gvcftools is a set of utilities to help create and analyze Genome VCF (gVCF) files.gVCF are VCF 4.1 files which follow a set of conventions for representing all sitesin the genome, further described at https://sites.google.com/site/gvcftools/home/about-gvcf. 0
gvcftools
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3.2.1 gubbins Gubbins - bacterial recombination detection Phylogeny Genotype and phenotype Whole genome sequencing Genotyping Phylogenetic inference Ancestral reconstruction 10253
gubbins
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357 gtftobed12 Convert GTF files to BED12 format Sequence analysis 21804
ucsc-gtftogenepred
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2.4.1 gtdbtk_classify_wf GTDB-Tk is a software tool kit for assigning objective taxonomic classifications to bacterial and archaeal genomesbased on the Genome Database Taxonomy GTDB. It is designed to work with recent advances that allow hundreds orthousands of metagenome-assembled genomes (MAGs) to be obtained directly from environmental samples. It can alsobe applied to isolate and single-cell genomes. Metagenomics Taxonomy Phylogenetics Database management Proteins Genome alignment Taxonomic classification Sequence assembly Query and retrieval 2418
gtdbtk
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0.1.9 gtdb_to_taxdump Convert GTDB taxonomy to NCBI taxdump format Computational biology Data handling Mapping Generation 449
gtdb_to_taxdump
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1.1.2 groot GROOT is a tool to type Antibiotic Resistance Genes (ARGs) in metagenomic samples Metagenomics Microbiology Genomics Antimicrobial resistance prediction 32
groot
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graphlan graphlan_annotate GraPhlAn is a software tool for producing high-quality circular representations of taxonomic and phylogenetic trees Metagenomics Phylogenetics Phylogenomics Cladistics Phylogenetic inference Phylogenetic tree visualisation Phylogenetic tree editing Taxonomic classification 14929
graphlan
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2.4 graphembed Compute a 2D embedding of a data matrix given supervised class information 208
graph_embed
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@TOOL_VERSION@+galaxy11 gprofiler_convert gprofiler_gost gprofiler_orth gprofiler_random gprofiler_snpense functional enrichment analysis of gene lists, convertion between various types of namespaces, translation gene identifiers between organisms and more 12462
r-gprofiler2
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1.50.0 goseq goseq does selection-unbiased testing for category enrichment amongst differentially expressed (DE) genes for RNA-seq data RNA-Seq Gene functional annotation 58501
bioconductor-goseq
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2.0.1 goenrichment goslimmer Performs GO Enrichment analysis. Transcriptomics Gene-set enrichment analysis 16687
goenrichment
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3.02 glimmer_acgt_content glimmer_build_icm glimmer_extract glimmer_gbk_to_orf glimmer_glimmer_to_gff glimmer_long_orfs glimmer_knowledge_based glimmer_not_knowledge_based Glimmer makes gene predictions. Sequence analysis Sequence analysis Genetic variation analysis 4543
glimmer
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1.0 emc-ggupset Create Upset Plots with ggupset 0
r-ggupset
To update
3.5.1 ggplot2_barplot ggplot2_boxplot ggplot2_heatmap ggplot2_pca ggplot2_histogram ggplot2_point ggplot2_violin ggplot2 is a system for declaratively creating graphics, based on The Grammar of Graphics.You provide the data, tell ggplot2 how to map variables to aesthetics, what graphical primitives to use,and it takes care of the details. Data visualisation Visualisation 69020
r-ggplot2
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0.12.7 gffread gffread filters and/or converts GFF3/GTF2 records Nucleic acids Sequence analysis Sequence annotation 46498
gffread
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0.12.10 gffcompare Galaxy wrappers for Geo Pertea's GffCompare package. Nucleic acids Sequence analysis Sequence annotation 14587
gffcompare
Up-to-date
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1.2 gff3.rebase Rebase a GFF against a parent GFF (e.g. an original genome) 1532
bcbiogff
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0.1.2 gfa_to_fa gfa_to_fa - Converting GFA format to Fasta format 18620
To update
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1.7.7.1 get_annotated_regions_from_gb get_organelle_from_reads GetOrganelle - This toolkit assembles organelle genomes from genomic skimming data. Cell biology Sequence assembly Whole genome sequencing Plant biology Model organisms De-novo assembly Genome assembly Mapping assembly Mapping Sequence trimming 3823
getorganelle
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0.5.9.2 get_hrun Annotate indel variants with homopolymer context 9
pyfaidx
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1.1.1 geopandas_table2geojson GeoPandas is an open source project to make working with geospatial data easier. 0
geopandas
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0.5+galaxy2 genrich Genrich is a peak-caller for genomic enrichment assays (e.g. ChIP-seq, ATAC-seq). 7256
genrich
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1.2.0 genomic_super_signature Interpretation of RNAseq experiments through robust, efficient comparison to public databases RNA-Seq Transcriptomics Microbial ecology Genotype and phenotype Microarray experiment Gene-set enrichment analysis Essential dynamics Deposition Principal component visualisation Dimensionality reduction 55
bioconductor-genomicsupersignature
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2.0.1 genomescope Analyze unassembled short reads 8540
genomescope2
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genetrack Contains a tool that separately identifies peaks on the forward "+” (W) and reverse “-” (C) strand. 670
numpy
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UseGalaxy.or1
4.7.1+galaxy1 gene_iobio_display_generation_iframe Gene.iobio is an interactive tool for variant and trio analysis. 245
To update
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3.0.0 genehunter_modscore Maximised LOD score pedigree analysis utility 0
ghm
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1.0.1+galaxy0 GeneBed_Maf_Fasta2 Stitch gene blocks given a set of coding exon intervals 2909
To update
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0.20.1 gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_db_info gemini_@BINARY@ gemini_@BINARY@ gemini_inheritance gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ gemini_@BINARY@ GEMINI: a flexible framework for exploring genome variation Sequence analysis Sequence analysis Genetic variation analysis 11577
gemini
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0.29.1 gem_check_memote gem_escher_visualization gem_extract_exchange gem_flux_distribution gem_flux_variability_analysis gem_knockout gem_phenotype_phase_plane Tools for analyzing genome-scale metabolic models (GEMs) using COBRApy and related libraries. 0
cobra
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1.2 gecko Ungapped genome comparison 1753
gecko
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1.0.0 data_source_gdcwebapp GDCWebApp automatically filter, extract, and convert genomic data from the Genomic Data Commons portal to BED format 0
python
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4.1.7.0 gatk4_mutect2 A Galaxy wrapper for Mutect2 from GATK 13833
gatk4
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2.2 gamma_s gamma Gene Allele Mutation Microbial Assessment 0
GAMMA
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1.8.17 funannotate_annotate funannotate_clean funannotate_compare funannotate_predict funannotate_sort Funannotate is a genome prediction, annotation, and comparison software package. Genomics Genome annotation 20216
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1.0.2 fsd fsd_beforevsafter fsd_regions td Tool that plots a histogram of sizes of read families 602
matplotlib
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UseGalaxy.or4
2.0.0 freyja_aggregate_plot freyja_boot freyja_demix freyja_variants lineage abundances estimation Metagenomics RNA-Seq quantification 24846
freyja
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11.6 control_freec Control-FREEC is a tool for detection of copy-number changes and allelic imbalances (including LOH) using deep-sequencing data originally developed by the Bioinformatics Laboratory of Institut Curie (Paris). It automatically computes, normalizes, segments copy number and beta allele frequency (BAF) profiles, then calls copy number alterations and LOH. DNA structural variation Oncology Human genetics Data mining Copy number estimation Variant calling Genome alignment 1528
gawk
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1.3.10 freebayes bamleftalign Galaxy Freebayes Bayesian genetic variant detector tool Genomics Genetic variation Rare diseases Variant calling Statistical calculation 479485
freebayes
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fraggenescan Tool for finding (fragmented) genes in short read Genetics Sequence analysis Gene prediction 2671
fraggenescan
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1.2.11 flash Fast Length Adjustment of SHort reads Sequencing Sequence assembly Read pre-processing Sequence merging Sequence assembly 43194
flash
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1.5 flair_collapse flair_correct FLAIR (Full-Length Alternative Isoform analysis of RNA) for the correction, isoform definition, and alternative splicing analysis of noisy reads. 2009
flair
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0.3.0 filtlong Filtlong - Filtering long reads by quality Filtering Sequencing quality control 111004
filtlong
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1.8.0+galaxy1 fgsea Perform gene set testing using fgsea Genetics Gene-set enrichment analysis 31468
bioconductor-fgsea
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r193 fermi2 fermikit_variants FermiKit is a de novo assembly based variant calling pipeline for deep Illumina resequencing data. 0
fermi2
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0.2.1 feelnc Galaxy wrapper for FEELnc RNA-seq Functional, regulatory and non-coding RNA Annotation Classification 2881
feelnc
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2.1.1 featurecounts featureCounts counts the number of reads aligned to defined masked regions in a reference genome RNA-Seq Read summarisation RNA-Seq quantification 1806783
subread
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2.1.10 fasttree FastTree infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences - GVL Phylogenetics Sequence analysis Phylogenetic tree generation (from molecular sequences) Phylogenetic tree generation (maximum likelihood and Bayesian methods) 109499
fasttree
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1.0.0 fastspar fastspar_pvalues fastspar_reduce Tool for rapid and scalable correlation estimation for compositional data. Metagenomics Microbial ecology 0
fastspar
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0.3.1+galaxy0 fastqe FASTQE Sequence analysis Sequencing Sequencing quality control 21008
fastqe
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0.74+galaxy1 fastqc Read QC reports using FastQC Sequencing Data quality management Sequence analysis Sequence composition calculation Sequencing quality control Statistical calculation 6372191
fastqc
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3.0.1 fastq_dl Download FASTQ files from ENA. 148
fastq-dl
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0.4.1 fastplong Fastplong is used for ultrafast preprocessing and quality control for long reads (Nanopore, PacBio, Cyclone, etc.). 0
fastplong
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1.0.1 fastp Fast all-in-one preprocessing for FASTQ files Sequence analysis Probes and primers Sequencing quality control Sequence contamination filtering 1778285
fastp
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1.1.0 fastk_fastk fastk_histex fastk_logex FastK: A K-mer counter (for HQ assembly data sets) Genomics Sequence analysis k-mer counting Sequence analysis 168
fastk
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1.3 fastani Fast alignment-free computation of whole-genome Average Nucleotide Identity Microbiology Genetic variation Genome alignment Sequence similarity search 26914
fastani
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2.0 fasta-stats Display summary statistics for a fasta file. 106138
numpy
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1.0.1 fasta_nucleotide_color_plot Contains a tool that produces a graphical representation of FASTA data with each nucleotide represented by a selected color. 1240
openjdk
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0.1 fargene fARGene (Fragmented Antibiotic Resistance Gene iENntifiEr ) Metagenomics Microbiology Public health and epidemiology Antimicrobial resistance Antimicrobial resistance prediction 1901
fargene
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1.2.4 falco A high throughput sequence QC analysis tool Workflows Mapping Imaging Sequencing quality control Visualisation Read mapping 6198
falco
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0.5.8 fairy_cov fairy_sketch Fast approximate contig coverage for metagenomic binning Metagenomics Read binning Sequence assembly validation 13
fairy
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3.0.3+galaxy3 Extract genomic DNA 1 Contains a tool that extracts genomic DNA using coordinates from ASSEMBLED genomes and UNassembled genomes. 274193
bx-python
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0.20 export2graphlan export2graphlan is a conversion software tool for producing both annotation and tree file for GraPhlAn Taxonomy Metabolomics Biomarkers Conversion 7678
export2graphlan
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2.4.0 exonerate Exonerate is a generic tool for pairwise sequence comparison. Sequence analysis Sequence sites, features and motifs Molecular interactions, pathways and networks Pairwise sequence alignment Protein threading Genome alignment 3882
exonerate
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1.1.0 exomedepth ExomeDepth: Calls copy number variants (CNVs) from targeted sequence data Exome sequencing Gene transcripts Mapping Sequencing Genetic variation Rare diseases Sequence analysis Variant calling Genotyping Copy number estimation 3638
r-exomedepth
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2.1.0 evidencemodeler EVidenceModeler (EVM) combines ab intio genetic predictions with protein and transcript alignments in weighted consensus genetic structures. Gene expression Gene structure Gene prediction 9
evidencemodeler
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0.6.7 eukrep Classification of Eukaryotic and Prokaryotic sequences from metagenomic datasets Metagenomics Nucleic acid sequence analysis 0
eukrep
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3.1.3 ete_treeviewer A toolkit for the analysis and visualization of trees. Phylogenetics Phylogenetic analysis Phylogenetic tree editing 0
ete
curl
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0.3.2 episcanpy_build_matrix episcanpy_cluster_embed episcanpy_preprocess EpiScanpy – Epigenomics single cell analysis in python Epigenomics Cell biology DNA Enrichment analysis Imputation 1689
episcanpy
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114.2 ensembl_vep Ensembl VEP: Annotate VCFs with variant effect predictions 3475
ensembl-vep
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enasearch_retrieve_analysis_report enasearch_retrieve_data enasearch_retrieve_run_report enasearch_retrieve_taxons enasearch_search_data A Python library for interacting with ENA's API 2361
enasearch
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8.1.1 ena_webin_cli Submits a genome assembly to the European Nucleotide Archive (ENA) using the Webin-CLI Submission tool. 0
ena-webin-cli
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0.9.0 ena_upload Submits experimental data and respective metadata to the European Nucleotide Archive (ENA). 1909
ena-upload-cli
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5.0.0 EMBOSS: antigenic1 EMBOSS: backtranseq2 EMBOSS: banana3 EMBOSS: biosed4 EMBOSS: btwisted5 EMBOSS: cai6 EMBOSS: cai_custom6 EMBOSS: chaos7 EMBOSS: charge8 EMBOSS: checktrans9 EMBOSS: chips10 EMBOSS: cirdna11 EMBOSS: codcmp12 EMBOSS: coderet13 EMBOSS: compseq14 EMBOSS: cpgplot15 EMBOSS: cpgreport16 EMBOSS: cusp17 EMBOSS: cutseq18 EMBOSS: dan19 EMBOSS: degapseq20 EMBOSS: descseq21 EMBOSS: diffseq22 EMBOSS: digest23 EMBOSS: dotmatcher24 EMBOSS: dotpath25 EMBOSS: dottup26 EMBOSS: dreg27 EMBOSS: einverted28 EMBOSS: epestfind29 EMBOSS: equicktandem31 EMBOSS: est2genome32 EMBOSS: etandem33 EMBOSS: extractfeat34 EMBOSS: extractseq35 EMBOSS: freak36 EMBOSS: fuzznuc37 EMBOSS: fuzzpro38 EMBOSS: fuzztran39 EMBOSS: garnier40 EMBOSS: geecee41 EMBOSS: getorf42 EMBOSS: helixturnhelix43 EMBOSS: hmoment44 EMBOSS: iep45 EMBOSS: infoseq46 EMBOSS: isochore47 EMBOSS: lindna48 EMBOSS: marscan49 EMBOSS: maskfeat50 EMBOSS: maskseq51 EMBOSS: matcher52 EMBOSS: megamerger53 EMBOSS: merger54 EMBOSS: msbar55 EMBOSS: needle56 EMBOSS: newcpgreport57 EMBOSS: newcpgseek58 EMBOSS: newseq59 EMBOSS: noreturn60 EMBOSS: notseq61 EMBOSS: nthseq62 EMBOSS: octanol63 EMBOSS: oddcomp64 EMBOSS: palindrome65 EMBOSS: pasteseq66 EMBOSS: patmatdb67 EMBOSS: pepcoil68 EMBOSS: pepinfo69 EMBOSS: pepnet70 EMBOSS: pepstats71 EMBOSS: pepwheel72 EMBOSS: pepwindow73 EMBOSS: pepwindowall74 EMBOSS: plotcon75 EMBOSS: plotorf76 EMBOSS: polydot77 EMBOSS: preg78 EMBOSS: prettyplot79 EMBOSS: prettyseq80 EMBOSS: primersearch81 EMBOSS: revseq82 EMBOSS: seqmatchall83 EMBOSS: seqret84 EMBOSS: showfeat85 EMBOSS: shuffleseq87 EMBOSS: sigcleave88 EMBOSS: sirna89 EMBOSS: sixpack90 EMBOSS: skipseq91 EMBOSS: splitter92 EMBOSS: supermatcher95 EMBOSS: syco96 EMBOSS: tcode97 EMBOSS: textsearch98 EMBOSS: tmap99 EMBOSS: tranalign100 EMBOSS: transeq101 EMBOSS: trimest102 EMBOSS: trimseq103 EMBOSS: twofeat104 EMBOSS: union105 EMBOSS: vectorstrip106 EMBOSS: water107 EMBOSS: wobble108 EMBOSS: wordcount109 EMBOSS: wordmatch110 Galaxy wrappers for EMBOSS version 5.0.0 tools Molecular biology Sequence analysis Biology Sequence analysis Local alignment Sequence alignment analysis Global alignment Sequence alignment 601921
emboss
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6.6.0 emboss_needle emboss_needleall Galaxy wrappers for EMBOSS6 tools Molecular biology Sequence analysis Biology Sequence analysis Local alignment Sequence alignment analysis Global alignment Sequence alignment 2
emboss
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1.20.0 egsea This tool implements the Ensemble of Gene Set Enrichment Analyses (EGSEA) method for gene set testing Systems biology Gene set testing 10922
bioconductor-egsea
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3.36.0 edger Perform RNA-Seq differential expression analysis using edgeR pipeline Genetics RNA-Seq ChIP-seq Differential gene expression analysis 93817
bioconductor-edger
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0.1.1 ebi_search_rest_results Tools to query and download data from several EMBL-EBI databases 1880
six
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0.1.2 drug2cell Collection of utility functions for gene group activity evaluation in scanpy. 0
drug2cell
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1.10.0 dropletutils DropletUtils - Utilities for handling droplet-based single-cell RNA-seq data Gene expression RNA-seq Sequencing Transcriptomics Loading Community profiling 11501
bioconductor-dropletutils
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3.6.2 drep_compare drep_dereplicate dRep compares and dereplicates genome sets Metagenomics Genomics Sequence analysis Genome comparison 1572
drep
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1.5.0 dram_annotate dram_distill dram_merge_annotations dram_neighborhoods dram_strainer DRAM for distilling microbial metabolism to automate the curation of microbiome function Metagenomics Biological databases Molecular genetics Gene functional annotation 7707
dram
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7.5.2 dos2unix dos2unix convert text files with DOS or Mac line breaks to Unix line breaks and vice versa. 0
dos2unix
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1.0.2 dnaweaver Given a SBOL input, calculate assembly parts for Gibson or Golden Gate. 0
dnaweaver_synbiocad
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3.1.0 dnabot DNA assembly using BASIC on OpenTrons 0
dnabot
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disco DISCO is a overlap-layout-consensus (OLC) metagenome assembler Structure determination Protein sequence analysis 1876
disco
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0.2.4 dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ dimet_@EXECUTABLE@ DIMet is a bioinformatics pipeline for differential analysis of isotopic targeted labeling data. 0
dimet
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1.1.3 diffdock Diffusion Steps, Twists, and Turns for Molecular Docking. 0
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3.12.0 diffbind Diffbind provides functions for processing ChIP-Seq data. ChIP-seq Differential binding analysis 30194
bioconductor-diffbind
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2.1.13 bg_diamond bg_diamond_makedb bg_diamond_view DIAMOND is a new alignment tool for aligning short DNA sequencing reads to a protein reference database such as NCBI-NR. Sequence analysis Proteins Sequence alignment analysis 161526
diamond
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1.48.0 dexseq dexseq_count plotdexseq Inference of differential exon usage in RNA-Seq RNA-Seq Enrichment analysis Exonic splicing enhancer prediction 51988
bioconductor-dexseq
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2.11.40.8 deseq2 Differential gene expression analysis based on the negative binomial distribution RNA-Seq Differential gene expression analysis RNA-Seq analysis 407449
bioconductor-deseq2
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0.9.1 delly_call delly_classify delly_cnv delly_filter delly_lr delly_merge Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome. DNA structural variation Sequencing Pathology Genomics Genetic variation Bioinformatics Population genomics Rare diseases Indel detection Structural variation detection Variant calling Genotyping Genetic variation analysis 1823
delly
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1.1.0+galaxy1 deg_annotate Annotate DESeq2/DEXSeq output tables RNA-Seq analysis Gene functional annotation 67834
bedtools
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1.5.0 deepvariant DeepVariant is a deep learning-based variant caller 8283
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1.2.5 deepsig Predictor of signal peptides in proteins based on deep learning 182
deepsig
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1.4 deepmicro Representation learning and classification framework Microbial ecology Machine learning Pathology Public health and epidemiology Allergy, clinical immunology and immunotherapeutics Essential dynamics Splitting Community profiling 559
deepmicro
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1.0.4 deeparg_predict deeparg_short_reads A deep learning based approach to predict Antibiotic Resistance Genes (ARGs) from metagenomes Microbiology Antimicrobial resistance prediction Antimicrobial resistance prediction 0
deeparg
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1.0.0 decontaminator Deep Learning method for novel virus detection in sequencing data Metagenomics Filtering 136
numpy
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1.22.0 decontam Removes decontamination features (ASVs/OTUs) using control samples Metagenomics Microbial ecology Sequencing Classification 1
bioconductor-decontam
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1.9 datamash_ops datamash_reverse datamash_transpose GNU Datamash is a command-line program which performs basicnumeric,textual and statistical operations on input textual data files.It is designed to be portable and reliable, and aid researchersto easily automate analysis pipelines, without writing code or even short scripts.License: GPL Version 3 (or later).These tool wrappers were originally writen by Assaf Gordon. 979675
datamash
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1.0.0 data_source_iris_tcga IRIS-TCGA Data source tool 0
python
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1.1.7 Fasta_to_Contig2Bin das_tool DAS Tool for genome resolved metagenomics Metagenomics Read binning 5527
das_tool
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1.34.0 dada2_assignTaxonomyAddspecies dada2_dada dada2_filterAndTrim dada2_learnErrors dada2_makeSequenceTable dada2_mergePairs dada2_plotComplexity dada2_plotQualityProfile dada2_primerCheck dada2_removeBimeraDenovo dada2_seqCounts DADA2 wrappers Sequencing Genetic variation Microbial ecology Metagenomics Variant calling DNA barcoding 379190
bioconductor-dada2
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1.1.1 cwpair2 Contains a tool that takes a list of called peaks on both strands and produces a list of matched pairsand a list of unmatched orphans. 281
matplotlib
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2.1.2 cutesv Long-read sequencing enables the comprehensive discovery of structural variations (SVs). However, it is still non-trivial to achieve high sensitivity and performance simultaneously due to the complex SV characteristics implied by noisy long reads. Therefore, we propose cuteSV, a sensitive, fast and scalable long-read-based SV detection approach. cuteSV uses tailored methods to collect the signatures of various types of SVs and employs a clustering-and-refinement method to analyze the signatures to implement sensitive SV detection. Benchmarks on real Pacific Biosciences (PacBio) and Oxford Nanopore Technology (ONT) datasets demonstrate that cuteSV has better yields and scalability than state-of-the-art tools. DNA structural variation Sequencing Computer science Split read mapping Genotyping Structural variation detection 424
cutesv
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5.1 cutadapt Flexible tool to remove adapter sequences (and quality trim) high throughput sequencing reads (fasta/fastq). Genomics Probes and primers Sequencing Sequence trimming Primer removal Read pre-processing 817890
cutadapt
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0.7.3 crossmap_bam crossmap_bed crossmap_bw crossmap_gff crossmap_region crossmap_vcf crossmap_wig CrossMap converts genome coordinates or annotation files between genome assemblies 7755
crossmap
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0.3 crosscontamination_barcode_filter Barcode contamination discovery tool Filtering Sequence contamination filtering Sequencing quality control RNA-Seq analysis 553
r-ggplot2
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1+galaxy0 crispr_studio CRISPR Studio is a program developed to facilitate and accelerate CRISPR array visualization. Sequence analysis Genomics Data visualisation Visualisation 2090
crispr_studio
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1.1.0 cramino A tool for quick quality assessment of cram and bam files, intended for long read sequencing. 0
cramino
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0.7.0 coverm_contig coverm_genome CoverM genome and contig wrappers Metagenomics Sequence analysis Local alignment 1917
coverm
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0.0.4 CoverageReport2 Generate Detailed Coverage Report from BAM file 0
perl-number-format
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1.0.1 cosg Marker gene identification for single-cell sequencing data using COSG. Bioinformatics Nucleic acid sequence analysis 0
cosg
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1.1.3 coreprofiler_allele_calling CoreProfiler, a tool for cgMLST allele calling from bacterial genome assemblies Microbiology Bioinformatics Phylogenetics Multilocus sequence typing 0
coreprofiler
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1.1.0 concoct concoct_coverage_table concoct_cut_up_fasta concoct_extract_fasta_bins concoct_merge_cut_up_clustering CONCOCT (Clustering cONtigs with COverage and ComposiTion) does unsupervised binning of metagenomic contigs byusing nucleotide composition - kmer frequencies - and coverage data for multiple samples. CONCOCT can accurately(up to species level) bin metagenomic contigs. Metagenomics Sequence clustering Read binning 8370
concoct
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0.1.0 compress_file Compress files. 25921
gzip
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0.1.1 compose_text_param Compose a text parameter value using text, integer and float values 60897
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0.2.6 compleasm Compleasm: a faster and more accurate reimplementation of BUSCO Sequence assembly Genomics Transcriptomics Sequence analysis Sequence assembly validation 995
compleasm
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1.0.4 comebin Binning of metagenomic contigs using COntrastive Multi-viEw representation learning 0
comebin
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1.0 column_remove_by_header Remove columns by header 17627
python
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0.0.1 column_order_header_sort Sort Column Order by heading 6596
python
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2.1 Add_a_column1 Compute an expression on every row 4769937
python
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0.0.2 collection_element_identifiers Extract element identifiers of a collection 21953
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0.0.3 collection_column_join Column Join on Collections 61363
coreutils
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24.7.14 commet discosnp_rad discosnp_pp kissplice lordec mapsembler2 takeabreak Colib'read tools are all dedicated to the analysis of NGS datasets without the need of any reference genome 1626
commet
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1.5.5 colabfold_alphafold colabfold_msa Protein prediction based on AlphaFold2 Protein folds and structural domains Protein folding, stability and design Structure prediction Sequence sites, features and motifs Metagenomics Database search Protein structure prediction Fold recognition 9177
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0.9.3 cooc_mutbamscan cooc_pubmut cooc_tabmut co-occurrence of mutations on amplicons Genetic variation 2779
cojac
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4.9 codeml Detects positive selection Phylogenetics Sequence analysis Probabilistic sequence generation Phylogenetic tree generation (maximum likelihood and Bayesian methods) Phylogenetic tree analysis 62370
paml
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0.9.12 cnvkit_access cnvkit_antitarget cnvkit_autobin cnvkit_batch cnvkit_export_bed cnvkit_breaks cnvkit_call cnvkit_export_cdt cnvkit_coverage cnvkit_diagram cnvkit_fix cnvkit_genemetrics cnvkit_heatmap cnvkit_export_jtv cnvkit_export_nexus_basic cnvkit_export_nexus_ogt cnvkit_reference cnvkit_scatter cnvkit_export_seg cnvkit_segment cnvkit_segmetrics cnvkit_sex cnvkit_target cnvkit_theta cnvkit_export_vcf detecting copy number variants and alterations genome-wide from high-throughput sequencing DNA structural variation Variant calling 1130
cnvkit
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2.0.0 cnv_vcf2json cnv-vcf2json Converts structural variants VCF file to JSON. 13
cnv-vcf2json
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1.0.2 cnv_phenopacket cnv-phenopacket Converts TSV metadata file to JSON. 7
cnv-phenopacket
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1.1.1 clustering_from_distmat Distance matrix-based hierarchical clustering using SciPy 123
python
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2.1 clustalw ClustalW multiple sequence alignment program for DNA or proteins Phylogeny Sequence analysis Multiple sequence alignment 195886
clustalw
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1.0.10 clair3 Symphonizing pileup and full-alignment for high-performance long-read variant calling Molecular genetics Variant calling 5081
clair3
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1.4.4 cite_seq_count Count CMO/HTO Transcriptomics Immunoproteins and antigens RNA-Seq quantification 174
cite-seq-count
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0.69.8 circos_aln_to_links circos_binlinks circos_bundlelinks circos circos_gc_skew circos_resample circos_wiggle_to_scatter circos_wiggle_to_stacked circos_tableviewer circos_interval_to_text circos_interval_to_tile Build Circos Plots in Galaxy Sequence visualisation 91641
circos
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2.3.8 circexplorer2 Comprehensive and integrative circular RNA analysis toolset. RNA splicing Gene transcripts Literature and language 806
circexplorer2
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1.1.4 cialign Tool to clean, visualise and analyse a multiple sequence alignment 0
cialign
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1.5.a chromeister ultra-fast pairwise genome comparisons 13108
chromeister
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0.10.0 chopper Filtering and trimming of fastq files with long read sequencing such as PacBio or ONT. 0
chopper
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1.0.9.post1 chopin2 Domain-Agnostic Supervised Learning with Hyperdimensional Computing 17
chopin2
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1.4.3 chira_collapse chira_extract chira_map chira_merge chira_quantify Chimeric Read Annotator for RNA-RNA interactome data RNA Molecular interactions, pathways and networks Functional, regulatory and non-coding RNA 42860
chira
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chewbbaca_allelecall chewbbaca_allelecallevaluator chewbbaca_createschema chewbbaca_downloadschema chewbbaca_extractcgmlst chewbbaca_joinprofiles chewbbaca_nsstats chewbbaca_prepexternalschema BSR-Based Allele Calling Algorithm 1302
chewbbaca
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0.7 cherri_eval cherri_train Computational Help Evaluating RNA-RNA interactions Molecular interactions, pathways and networks Structure analysis Machine learning 207
cherri
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1.0.2 checkm2 Rapid assessment of genome bin quality using machine learning Genomics Phylogenomics Phylogenetics Taxonomy Metagenomics Data quality management Sequence assembly validation Validation Sequence composition calculation Sequencing quality control Statistical calculation 0
checkm2
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1.2.4 checkm_analyze checkm_lineage_set checkm_lineage_wf checkm_plot checkm_qa checkm_taxon_set checkm_taxonomy_wf checkm_tetra checkm_tree checkm_tree_qa Assess the quality of microbial genomes recovered from isolates, single cells, and metagenomes Genomics Phylogenomics Phylogenetics Taxonomy Metagenomics Data quality management Sequence assembly validation Validation Sequence composition calculation Sequencing quality control Statistical calculation 11964
checkm-genome
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1.0.1 charts Enables advanced visualization options in Galaxy Charts 19379
r-getopt
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1.30.0 cemitool Gene co-expression network analysis tool Gene expression Transcriptomics Microarray experiment Enrichment analysis Pathway or network analysis 806
bioconductor-cemitool
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4.8.1 cd_hit Cluster or compare biological sequence datasets Sequencing Sequence clustering 13733
cd-hit
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5.2.3 cat_add_names cat_bins cat_contigs cat_prepare cat_summarise Contig Annotation Tool (CAT) Metagenomics Metagenomic sequencing Taxonomy Sequence assembly Taxonomic classification Sequence assembly Coding region prediction 18894
cat
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2.0.7 biobox_add_taxid cami_amber cami_amber_add cami_amber_convert Evaluation package for the comparative assessment of genome reconstructions and taxonomic assignments Metagenomics Read binning 8385
cami-amber
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0.1.0 calculate_numeric_param Calculate a numeric parameter value using integer and float values. 1724
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1.0.0 calculate_contrast_threshold Calculates a contrast threshold from the CDT file generated by ``tag_pileup_frequency``. The calculated values are then used to set a uniform contrast for all the heatmaps generated downstream. 0
numpy
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2.7.1 cactus_cactus cactus_export Cactus is a reference-free whole-genome multiple alignment program Genomics Sequence analysis Phylogeny Sequence assembly Mapping Phylogenetics Multiple sequence alignment Genome alignment 2834
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0.2.9 bwameth Fast and accurate alignment of BS-seq reads 21361
bwameth
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2.3 bwa_mem2_idx bwa_mem2 Bwa-mem2 is the next version of the bwa-mem algorithm in bwa. Mapping Sequence alignment 152689
bwa-mem2
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bwa
0.7.19 bwa_mem bwa Wrapper for bwa mem, aln, sampe, and samse Mapping Genome indexing Sequence alignment Read mapping Sequence alignment Generation Sequence alignment Generation Sequence alignment Sequence alignment 1858218
bwa
bwa
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5.8.0 busco BUSCO assess genome and annotation completeness Sequence assembly Genomics Transcriptomics Sequence analysis Sequence assembly validation 209510
busco
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1.0.2 brew3r_r Extend 3' end of a GTF using another GTF as a template Transcriptomics Genomics Genome annotation 12
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0.35.5 breseq Predicts mutations in microbial genomes Sequencing Sequence analysis DNA mutation Polymorphism detection 4203
breseq
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3.1 est_abundance Bayesian Reestimation of Abundance with KrakEN Metagenomics Microbial ecology Statistical calculation 104329
bracken
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2.5.3 bowtie2 Bowtie2: Fast and sensitive read alignment Mapping Genomics Mapping Read mapping 1520871
bowtie2
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1.1 blastxml_to_gapped_gff3 BlastXML to gapped GFF3 1122
bcbiogff
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1.7.0 magicblast Maps large next-generation RNA or DNA sequencing runs against a whole genome or transcriptome 6951
magicblast
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2.3.3 biscot Bionano scaffolding correction tool 3
biscot
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1.1 bp_genbank2gff3 Converts GenBank format files to GFF3 Genomics Software engineering Data management Data handling Service invocation 28460
perl-bioperl
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2.1.15 biom_add_metadata biom_convert biom_from_uc biom_normalize_table biom_subset_table biom_summarize_table The biom-format package provides a command line interface and Python API for working with BIOM files. Laboratory information management Sequence analysis Formatting 22711
biom-format
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0.1.0 fasta_regex_finder Miscellanea of scripts for bioinformatics 2692
python
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0.21.9 bioext_bam2msa bioext_bealign A suite of Galaxy tools designed around the BioExt extension to BioPython. Align sequences, merge duplicate sequences into one, and more! 49510
python-bioext
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1.4.3 bin_refiner Reconciles the outputs of different binning programs with the aim to improve the quality of genome bins,especially with respect to contamination levels. Metagenomics Sequence assembly Microbial ecology Read binning Sequence clustering 161
binning_refiner
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1.1.2 binette Binning refinement tool Metagenomics Read binning 0
binette
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0.2.4 bigwig_outlier_bed pybigtools and numpy code to find continuous runs above a high or below a low quantile cutpoint in bigwig files 1564
python
To update
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1.1.9 bigscape Construct sequence similarity networks of BGCs and groups them into GCF Phylogeny Microbial ecology Mapping Metabolomics Bioinformatics Gene and protein families Clustering Global alignment Fold recognition 1196
bigscape
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0.2.3 berokka Berokka is used to trim, circularise, orient & filter long read bacterial genome assemblies. 1024
berokka
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1.0 bellerophon Filter mapped reads where the mapping spans a junction, retaining the 5-prime read. 3799
bellerophon
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0.0.2 bellavista_prepare Open-Source Visualization for Imaging-Based Spatial Transcriptomics 0
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2.31.1 bedtools_annotatebed bedtools_bamtobed bedtools_bed12tobed6 bedtools_bedtobam bedtools_bedtoigv bedtools_bedpetobam bedtools_closestbed bedtools_clusterbed bedtools_complementbed bedtools_coveragebed bedtools_expandbed bedtools_fisher bedtools_flankbed bedtools_genomecoveragebed bedtools_getfastabed bedtools_groupbybed bedtools_intersectbed bedtools_jaccard bedtools_links bedtools_makewindowsbed bedtools_map bedtools_maskfastabed bedtools_mergebed bedtools_multicovtbed bedtools_multiintersectbed bedtools_nucbed bedtools_overlapbed bedtools_randombed bedtools_reldistbed bedtools_shufflebed bedtools_slopbed bedtools_sortbed bedtools_spacingbed bedtools_subtractbed bedtools_tagbed bedtools_unionbedgraph bedtools_windowbed bedtools is a powerful toolset for genome arithmetic Genomics Mapping 1782914
bedtools
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2.4.42 bedops-sort-bed BEDOPS: high-performance genomic feature operations 457
bedops
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5.4_29Oct24.c8e beagle Beagle is a program for phasing and imputing missing genotypes. 137
beagle
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2.0.0 beacon2_csv2xlsx beacon2_pxf2bff beacon2_vcf2bff beacon2-ri-tools are part of the ELIXIR-CRG Beacon v2 Reference Implementation (B2RI). Genetic variation Population genetics Data security Rare diseases Service discovery Database search Genetic variation analysis 52
beacon2-ri-tools
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2.2.4 beacon2_analyses beacon2_biosamples beacon2_bracket beacon2_cnv beacon2_cohorts beacon2_datasets beacon2_gene beacon2_import beacon2_individuals beacon2_range beacon2_runs beacon2_sequence Beacon Import uploads local genetic data to the server, while Beacon Query searches for genetic information such as genes, sequences, and variants. Genetic variation Population genetics Data security Rare diseases Service discovery Database search Genetic variation analysis 51
beacon2-import
Up-to-date
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0.2.2 bctools_convert_to_binary_barcode bctools_extract_crosslinked_nucleotides bctools_extract_alignment_ends bctools_extract_barcodes bctools_merge_pcr_duplicates bctools_remove_tail bctools_remove_spurious_events bctools is a set of tools for handling barcodes and UMIs in NGS data.bctools can be used to merge PCR duplicates according to unique molecular barcodes (UMIs),to extract barcodes from arbitrary positions relative to the read starts,to clean up readthroughs into UMIs with paired-end sequencing andhandles binary barcodes as used with uvCLAP and FLASH.License: Apache License 2.0 3130
bctools
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1.15.1 bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@_from_vcf bcftools_@EXECUTABLE@_to_vcf bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_plugin_@PLUGIN_ID@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@_list_samples bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ bcftools_@EXECUTABLE@ BCFtools toolkit wrappers Genetic variation DNA polymorphism GWAS study Genotyping experiment Data handling Variant calling 0
bcftools
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39.08 bbtools_bbduk bbtools_bbmap bbtools_bbmerge bbtools_bbnorm bbtools_callvariants bbtools_tadpole BBTools is a suite of fast, multithreaded bioinformatics tools designed for analysis of DNA and RNA sequence data.BBTools can handle common sequencing file formats such as fastq, fasta, sam, scarf, fasta+qual, compressed or raw,with autodetection of quality encoding and interleaving. It is written in Java and works on any platform supportingJava, including Linux, MacOS, and Microsoft Windows and Linux; there are no dependencies other than Java (version7 or higher). Program descriptions and options are shown when running the shell scripts with no parameters. Sequencing RNA splicing Whole genome sequencing Phylogenetics Metagenomics RNA-Seq RNA-Seq analysis Sequence trimming Read mapping Sequence contamination filtering Read binning Sequence alignment 26010
bbmap
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0.1 bbgtobigwig Make a coverage bigwig from bam, bed or gff, optionally with a chromosome length file. Sequence analysis 1082
ucsc-bedgraphtobigwig
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2.1 BayeScan Detecting natural selection from population-based genetic data Genetics Evolutionary biology Statistics and probability DNA polymorphism Statistical inference 104
bayescan
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0.0.11 bax2bam BAX to BAM converter 420
bax2bam
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1.2.0 basil Breakpoint detection, including large insertions 806
anise_basil
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1.2.2 barrnap Contains the Barrnap tool for finding ribosomal RNAs in FASTA sequences. Genomics Model organisms Model organisms Gene prediction 16098
barrnap
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1.1.3 baredsc_1d baredsc_2d baredsc_combine_1d baredsc_combine_2d baredSC is a tool that uses a Monte-Carlo Markov Chain to estimate a confidence interval on the probability density function (PDF) of expression of one or two genes from single-cell RNA-seq data. RNA-Seq Cytometry Transcriptomics Gene transcripts Statistics and probability Data retrieval Expression correlation analysis Differential gene expression profiling 315
baredsc
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0.18.4.0 barcode_splitter A utility to split sequence files using multiple sets of barcodes 0
barcode_splitter
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2022.09 bandage_image bandage_info Bandage - A Bioinformatics Application for Navigating De novo Assembly Graphs Easily Genomics Sequence assembly Sequence assembly visualisation 151833
bandage_ng
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bamutil_clip_overlap bamutil_diff bamUtil is a repository that contains several programs that perform operations on SAM/BAM files. 436
bamutil
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1.0.1 bam_to_scidx Contains a tool that converts a BAM file to an ScIdx file. 919
openjdk
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1.9.4 bakta "Bakta is a tool for the rapid & standardized annotation of bacterial genomes and plasmids from both isolates and MAGs.It provides dbxref-rich and sORF-including annotations in machine-readable JSON & bioinformatics standard file formats for automatic downstream analysis." Genomics Sequence analysis Bioinformatics Genome annotation 39052
bakta
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3.0.5+galaxy0 b2btools_single_sequence This software suite provides structural predictions for protein sequences made by Bio2Byte group.About Bio2Byte: We investigate how the dynamics, conformational states, and available experimental data of proteins relate to their amino acid sequence.Underlying physical and chemical principles are computationally unraveled through data integration, analysis, and machine learning, so connecting themto biological events and improving our understanding of the way proteins work. Protein disorder prediction Protein secondary structure prediction Protein feature detection 372
b2btools
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0.6.2 autobigs-cli Automated MLST typing from PubMLST and InstitutPasteur. 0
autobigs-cli
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3.5.0 augustus augustus_training AUGUSTUS is a program that predicts genes in eukaryotic genomic sequences. Gene transcripts Gene and protein families Gene prediction Ab-initio gene prediction Homology-based gene prediction Homology-based gene prediction Operation 45840
augustus
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5.7.8 astral Tool for estimating an unrooted species tree given a set of unrooted gene trees 151
astral-tree
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17.02 assembly_stats Assembly metric visualisations to facilitate rapid assessment and comparison of assembly quality. 26
rjchallis-assembly-stats
Up-to-date
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1.7.3 artic_guppyplex artic_minion The artic pipeline is designed to help run the artic bioinformatics protocols;for example the nCoV-2019 novel coronavirus protocol.Features include: read filtering, primer trimming, amplicon coverage normalisation,variant calling and consensus building Genomics Sequence alignment 12443
artic
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art
2014.11.03.0 art_454 art_illumina art_solid Simulator for Illumina, 454, and SOLiD sequencing data Bioinformatics Conversion 259
art
art
To update
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2.5.1 arriba arriba_draw_fusions arriba_get_filters Arriba detects fusion genes in RNA-Seq data after running RNA-STAR 4316
arriba
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1.0.0 argnorm argNorm is a tool to normalize antibiotic resistance genes (ARGs) by mapping them to the antibiotic resistance ontology (ARO) created by the CARD database Gene functional annotation 76
argnorm
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3.18.0 annotatemyids annotateMyIDs: get annotation for a set of IDs using the Bioconductor annotation packages Annotation 113317
bioconductor-org.hs.eg.db
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1.3.2 anndata2ri Convert between Anndata and SingCellExperiment objects Data handling 0
anndata2ri
To update
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0.10.9 anndata_export anndata_import anndata_inspect anndata_manipulate modify_loom Import, Export, Inspect and Manipulate Anndata and Loom objects 77315
anndata
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1.4.0 ancombc Performs analysis of compositions of microbiomes with bias correction. Microbial ecology Metagenomics Taxonomy DNA barcoding 37
bioconductor-ancombc
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3.12.8 amrfinderplus "AMRFinderPlus is designed to find acquired antimicrobial resistance genes and point mutations in protein and/or assembled nucleotide sequences.It can also search "plus", stress, heat, and biocide resistance and virulence factors for some organisms. Microbiology Public health and epidemiology Infectious disease Antimicrobial resistance prediction 19178
ncbi-amrfinderplus
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2.8.9 ampvis2_alpha_diversity ampvis2_boxplot ampvis2_core ampvis2_export_fasta ampvis2_export_otu ampvis2_frequency ampvis2_heatmap ampvis2_load ampvis2_merge_ampvis2 ampvis2_mergereplicates ampvis2_octave ampvis2_ordinate ampvis2_otu_network ampvis2_rankabundance ampvis2_rarecurve ampvis2_setmetadata ampvis2_subset_samples ampvis2_subset_taxa ampvis2_timeseries ampvis2_venn ampvis2 Biodiversity Analysis Visualisation 2712
To update
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2.0.1 ampligone AmpliGone is a tool which accurately finds and removes primer sequences from NGS reads in an amplicon experiment. 0
AmpliGone
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1.14.0 amplican AmpliCan is an analysis tool for genome editing. PCR experiment Statistics and probability Alignment Standardisation and normalisation 84
bioconductor-amplican
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2 allegro Linkage and haplotype analysis from deCODE Sequence analysis Transcription factors and regulatory sites DNA Sequence motif discovery 0
allegro
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1.26.0 aldex2 Performs analysis Of differential abundance taking sample variation into account Gene expression Statistics and probability Statistical inference 299
bioconductor-aldex2
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0.16.0 aegean_canongff3 aegean_gaeval aegean_locuspocus aegean_parseval AEGeAn toolkit wrappers Sequence analysis Gene structure Sequence annotation 2619
aegean
Up-to-date
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0.2.0 addName Add input name as column on an existing tabular file 121270
python
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2.3.4 adapter_removal Removes residual adapter sequences from single-end (SE) or paired-end (PE) FASTQ reads. Sequence trimming Sequence merging Primer removal 517
adapterremoval
Up-to-date
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2.3.10 abyss-pe Assembly By Short Sequences - a de novo, parallel, paired-end sequence assembler Sequence assembly Genome assembly De-novo assembly Scaffolding 9601
abyss
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1.0.19 abritamr A pipeline for running AMRfinderPlus and collating results into functional classes Microbiology Public health and epidemiology Infectious disease Antimicrobial resistance Antimicrobial resistance prediction 1663
abritamr
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1.0.1 abricate abricate_list abricate_summary Mass screening of contigs for antiobiotic resistance genes Genomics Microbiology Antimicrobial resistance prediction 1566054
abricate
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0.1.0 trimns TrimNs is used to trim and remove fake cut sites from bionano hybrid scaffold data in the VGP pipeline 48
trimns_vgp
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0.1.2 venn_list Draw Venn Diagram (PDF) from lists, FASTA files, etc 24966
galaxy_sequence_utils
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0.0.15 seq_select_by_id Select sequences by ID 4227
biopython
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0.0.10 seq_rename Rename sequences with ID mapping from a tabular file 0
galaxy_sequence_utils
To update
UseGalaxy.no1
0.0.18 seq_primer_clip Trim off 5' or 3' primers 0
galaxy_sequence_utils
To update
0.0.5 seq_length Compute sequence length (from FASTA, QUAL, FASTQ, SFF, etc) 0
biopython
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0.0.8 seq_filter_by_mapping Filter sequencing reads using SAM/BAM mapping files 4832
biopython
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0.2.9 seq_filter_by_id Filter sequences by ID 77309
biopython
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0.0.5 seq_composition Sequence composition 2162
biopython
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0.0.6 samtools_idxstats BAM mapping statistics (using samtools idxstats) 201323
samtools
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0.0.3 samtools_depth Coverage depth via samtools 18978
samtools
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0.0.5 samtools_depad Re-align a SAM/BAM file with a padded reference (using samtools depad) 0
samtools
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0.2.6 sample_seqs Sub-sample sequences files (e.g. to reduce coverage) 7307
biopython
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0.0.13 promoter2 Psortb rxlr_motifs signalp3 tmhmm2 wolf_psort TMHMM, SignalP, Promoter, RXLR motifs, WoLF PSORT and PSORTb 13659
promoter
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0.0.10 predictnls Python reimplementation of predictNLS for Galaxy 0
To update
0.0.11 nlstradamus Find nuclear localization signals (NLSs) in protein sequences 0
NLStradamus
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0.0.8 mummerplot_wrapper Draw dotplots using mummer, mucmer, or promer with mummerplot 2052
ghostscript
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0.2.3 get_orfs_or_cdss Search nucleotide sequences for open reading frames (ORFs), or coding sequences (CDSs) 2684
biopython
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0.1.5 fastq_paired_unpaired Divide FASTQ file into paired and unpaired reads 0
galaxy_sequence_utils
To update
0.0.5 fastq_pair_names Extract FASTQ paired read names 0
galaxy_sequence_utils
To update
0.0.7 fastq_filter_by_id Filter FASTQ sequences by ID (DEPRECATED) 0
galaxy_sequence_utils
To update
0.0.7 fasta_filter_by_id Filter FASTA sequences by ID (DEPRECATED) 0
galaxy_sequence_utils
To update
0.0.21 effectiveT3 Find bacterial type III effectors in protein sequences Sequence analysis Sequence classification 0
effectiveT3
To update
0.1.0 coverage_stats BAM coverage statistics using samtools idxstats and depth 0
samtools
To update
0.0.6 count_roi_variants Count sequence variants in region of interest in BAM file 0
samtools
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0.1.0 clinod NoD: a Nucleolar localization sequence detector for eukaryotic and viral proteins Sequence analysis Nucleic acid sequence analysis 559
clinod
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0.0.7 clc_assembler clc_mapper Galaxy wrapper for the CLC Assembly Cell suite from CLCBio 0
samtools
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0.0.3 chromosome_diagram Chromosome Diagrams using Biopython 0
biopython
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0.0.10 align_back_trans Thread nucleotides onto a protein alignment (back-translation) 588
biopython
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2.5 wtdbg WTDBG is a fuzzy Bruijn graph (FBG) approach to long noisy reads assembly. Sequence assembly Sequencing Genome assembly De-novo assembly 1968
wtdbg
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1.9.4 wordcloud A little word cloud generator in Python. 12
wordcloud
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3.4.2 whisperx Transcribe audio or video files to text using the OpenAI Whisper and speaker diarization using pyannote audio 0
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20231117 whisper Transcribe audio or video files to text using the OpenAI Whisper. 234
To update
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vt
0.2 vt_@BINARY@ vt_@BINARY@ A tool set for short variant discovery in genetic sequence data. 0
vt
To update
1.1.0 vrhyme Tool for dereplication and binning virus genomes from metagenomes. Metagenomics Microbial ecology Model organisms Machine learning Sequence assembly Scaffolding Read binning Read mapping Sequence trimming 0
vrhyme
Up-to-date
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vpt
1.3.0 vpt_extract vpt_segment Vizgen Post-processing Tool 0
To update
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0.7 uniprot UniProt ID mapping and sequence retrieval 9659
requests
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0.6.10 trim_galore Trim Galore adaptive quality and adapter trimmer Sequence analysis Sequence trimming Primer removal Read pre-processing 738950
trim-galore
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0.0.5 create_tool_recommendation_model Create model to recommend tools 522
python
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1.0.3 tiara Tool for identification of eukaryotic sequences in the metagenomic datasets. Sequencing Genomics DNA polymorphism DNA structural variation Genome comparison Data retrieval Variant calling Genome visualisation Structural variation detection 296
tiara
To update
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1.0.3 tgsgapcloser TGS-GapCloser uses error-prone long reads or preassembled contigs to fill N-gap in the genome assembly. Sequencing Sequence assembly Phylogeny Transcription factors and regulatory sites Mapping Genome assembly Read mapping Scaffolding Localised reassembly 552
tgsgapcloser
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9.5 tp_awk_tool tp_cat tp_cut_tool tp_easyjoin_tool tp_find_and_replace tp_grep_tool tp_head_tool tp_multijoin_tool nl tp_text_file_with_recurring_lines tp_replace_in_column tp_replace_in_line tp_sed_tool tp_sort_header_tool tp_sort_rows tp_uniq_tool tp_tac tp_tail_tool tp_unfold_column_tool tp_sorted_uniq High performance text processing tools using the GNU coreutils, sed, awk and friends. 5378481
coreutils
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0.5.2 split_file_to_collection Split tabular, MGF, FASTA, or FASTQ files to a dataset collection. 34449
python
To update
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0.6 tp_split_on_column Split a file on a specific column. 9569
gawk
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1.0.1 join_files_on_column_fuzzy Join two files on a common column, allowing a certain difference. 3939
python
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0.2 bg_column_arrange_by_header Column arrange by header name 11739
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0.1.0 add_line_to_file Adds a text line to the beginning or end of a file. 20235
coreutils
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4.76+galaxy0 tapscan_classify Search for transcription associated proteins (TAPs) 38
hmmer
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2.0.9 tabpfn Tabular data prediction using TabPFN using Pytorch. 73
tabpfn
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0.8.1 sylph_profile sylph_query sylph - fast and precise species-level metagenomic profiling with ANIs Metagenomics Taxonomic classification 0
sylph
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0.12.04 stress_ng stress test a computer system in various selectable ways 62
stress-ng
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0.3 bg_statistical_hypothesis_testing Tool for computing statistical tests. 365
numpy
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0.5.0 rbc_splitfasta Split a multi-sequence fasta file into files containing single sequences 6146
biopython
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1.0.11.0 sklearn_mlxtend_association_rules sklearn_clf_metrics sklearn_discriminant_classifier sklearn_ensemble sklearn_estimator_attributes sklearn_feature_selection sklearn_fitted_model_eval sklearn_generalized_linear keras_batch_models keras_model_builder keras_model_config keras_train_and_eval sklearn_label_encoder sklearn_lightgbm ml_visualization_ex model_prediction sklearn_model_validation sklearn_nn_classifier sklearn_numeric_clustering sklearn_pairwise_metrics sklearn_pca sklearn_build_pipeline sklearn_data_preprocess sklearn_regression_metrics sklearn_sample_generator sklearn_searchcv sklearn_model_fit scipy_sparse stacking_ensemble_models sklearn_svm_classifier sklearn_to_categorical sklearn_train_test_eval sklearn_train_test_split Machine Learning tool suite from Scikit-learn 162587
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0.2.0.4 segemehl segemehl - short read mapping with gaps 1308
segemehl
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0.0.1 sed_stream_editor Manipulate your data with the sed command line tool. 2284
sed
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1.0.1 sambamba_flagstat sambamba_markdup sambamba_merge sambamba_sort Sambamba: process your BAM data faster! 2714
sambamba
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1.10.1 alevin salmon salmonquantmerge Salmon is a wicked-fast program to produce a highly-accurate, transcript-level quantification estimates from RNA-seq and single-cell data. RNA-Seq Gene expression Transcriptomics Sequence composition calculation RNA-Seq quantification Gene expression analysis 235077
salmon
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0.10.1.1 sailfish Sailfish is a tool for transcript quantification from RNA-seq data 23247
bzip2
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2.2.10 viennarna_kinfold viennarna_kinwalker viennarna_rna2dfold viennarna_rnaaliduplex viennarna_rnaalifold viennarna_rnacofold viennarna_rnadistance viennarna_rnaduplex viennarna_rnaeval viennarna_rnafold viennarna_rnaheat viennarna_rnainverse viennarna_rnalalifold viennarna_rnalfold viennarna_rnapaln viennarna_rnadpdist viennarna_rnapkplex viennarna_rnaplex viennarna_rnaplfold viennarna_rnaplot viennarna_rnasnoop viennarna_rnasubopt viennarna_rnaup ViennaRNA - Prediction and comparison of RNA secondary structures 8297
viennarna
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0.6 aragorn_trna trnascan Aragorn predicts tRNA and tmRNA in nucleotide sequences. 8253
aragorn
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1.7 targetfinder Plant small RNA target prediction tool 2212
targetfinder
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1.0.7 sshmm ssHMM is an RNA sequence-structure motif finder for RNA-binding protein data, such as CLIP-Seq data 227
sshmm
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4.3.6 bg_sortmerna SortMeRNA is a software designed to rapidly filter ribosomal RNA fragments from metatransriptomic data produced by next-generation sequencers. Metatranscriptomics Metagenomics Sequence similarity search Sequence comparison Sequence alignment analysis 32066
sortmerna
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1.0.5 selectsequencesfrommsa SelectSequences - selects representative entries from a multiple sequence alignment in clustal format 473
selectsequencesfrommsa
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2.1.1 rnaz rnaz_annotate rnaz_cluster rnaz_randomize_aln rnaz_select_seqs rnaz_window RNAz is a program for predicting structurally conserved and thermodynamically stable RNA secondary structures in multiple sequence alignments. 43319
rnaz
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1.2.0 rnasnp RNAsnp Efficient detection of local RNA secondary structure changes induced by SNPs 95
rnasnp
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1.3.6 RNAlien RNAlien unsupervized RNA family model construction 33
rnalien
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1.2.0 infer_rnaformer RNAformer: RNA secondary structure prediction 76
rnaformer
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0.1.1 rbc_rnacommender RNAcommender is a tool for genome-wide recommendation of RNA-protein interactions. 1082
sam
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0.3.2 rbc_rnacode Analyze the protein coding potential in MSA 1363
rnacode
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2.2.1.0 rbc_rnabob Fast pattern searching for RNA structural motifs 198
rnabob
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3.3.0 RNAshapes Compute secondary structures of RNA 258
@EXECUTABLE@
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1.3.1a ribotaper_create_annotation ribotaper_create_metaplots ribotaper_ribosome_profiling A method for defining traslated ORFs using Ribosome Profiling data. Functional genomics Gene expression profiling 740
ribotaper
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1.0.0 remurna remuRNA - Measurement of Single Nucleotide Polymorphism induced Changes of RNA Conformation 66
remurna
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1.1 reago Reago is tool to assembly 16S ribosomal RNA recovery from metagenomic data. Sequence assembly RNA Metagenomics Microbiology Sequence assembly 1
reago
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1.5.4 rcas RCAS (RNA Centric Annotation System) for functional analysis of transcriptome-wide regions detected by high-throughput experiments 1271
bioconductor-rcas
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0.8.1 rbpbench Evaluate CLIP-seq and other genomic region data using a comprehensive collection of RBP binding motifs RNA Protein interactions RNA immunoprecipitation Bioinformatics Sequence analysis 109
rbpbench
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0.1 meta_rna Identification of ribosomal RNA genes in metagenomic fragments. 0
hmmsearch3.0
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0.1.0 pipmir A method to identify novel plant miRNA. 312
pipmir
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1.5 paralyzer A method to generate a high resolution map of interaction sites between RNA-binding proteins and their targets. 356
paralyzer
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1.0 nastiseq A method to identify cis-NATs using ssRNA-seq 42
r-nastiseq
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mqc
1.9 mqc Ribosome profiling mapping quality control tool 76
mqc
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mea
0.6.4.1 mea Maximum expected accuracy prediction 86
mea
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2.0.1 locarna_exparnap locarna_multiple locarna_pairwise locarna_pairwise_p locarna_reliability_profile LocARNA - A suite for multiple alignment and folding of RNAs 358
locarna
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Kinwalker splits the folding process into a series of events where each event can either be a folding event or a transcription event. 0
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3.4.1 intarna Efficient RNA-RNA interaction prediction incorporating accessibility and seeding of interaction sites. 7713
intarna
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INFO-RNA is a service for the design of RNA sequences that fold into a given pseudo-knot free RNA secondary structure. 0
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1.1.5 infernal_cmalign infernal_cmbuild infernal_cmpress infernal_cmscan infernal_cmsearch infernal_cmstat Infernal ("INFERence of RNA ALignment") is for searching DNA sequence databases for RNA structure and sequence similarities. Sequence sites, features and motifs Structural genomics Nucleic acid feature detection 116069
infernal
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0.1.0+galaxy0 htseq_clip htseq-clip is a toolset for the analysis of eCLIP/iCLIP datasets 106
htseq-clip
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1.1.7+galaxy2 graphprot_predict_profile GraphProt models binding preferences of RNA-binding proteins. 496
graphprot
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1.0.1 exparna ExpaRNA is a fast, motif-based comparison and alignment tool for RNA molecules. 0
exparna
Up-to-date
1.3.1 dotknot DotKnot is a heuristic method for pseudoknot prediction in a given RNA sequence 88
vienna_rna
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5.7.a rnastructure_dot2ct Dot-Bracket to Connect Table (CT) 0
rnastructure
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1.0 dorina_search data source for RNA interactions in post-transcriptional regulation 1639
To update
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0.1.0+galaxy0 dewseq DEWSeq is a sliding window based peak caller for eCLIP/iCLIP data 96
python
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2.1.1 coprarna Target prediction for prokaryotic trans-acting small RNAs 0
coprarna
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1.0 compalignp Compute fractional identity between trusted alignment and test alignment 222
compalignp
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2.0.4.0 cofold Cofold predicts RNA secondary structures that takes co-transcriptional folding into account. 361
cofold
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cmv
1.0.8 cmcv cmv hmmcv hmmv cmv is a collection of tools for the visualisation of Hidden Markov Models and RNA-family models. 114
cmv
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0.08+galaxy2 cmsearch_deoverlap removes lower scoring overlaps from cmsearch results. Biology Medicine Comparison Alignment 2982
perl
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1.1.1 blockclust BlockClust detects transcripts with similar processing patterns. 2288
blockclust
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0.1.2 AREsite2_REST AREsite2 REST Interface 76
python
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1.1 antarna antaRNA uses ant colony optimization to solve the inverse folding problem in RNA research . 306
antarna
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0.1.0 pubchem_rest_tool This tool fetches data from pubchem via the PubChem REST API. 0
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0.2 replace_column_with_key_value_file A tool to replace all column entries of a file given by values of a key-value file. 626596
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0.1.2 repeatmasker_wrapper RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences. 21398
RepeatMasker
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1.5.0 racon Consensus module for raw de novo DNA assembly of long uncorrected reads. Whole genome sequencing Sequence assembly Genome assembly Mapping assembly 53784
racon
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2022.11.1+galaxy0 qiime2_dbotu_q2 q2-dbotu is a Qiime 2 plugin for performing OTU clustering Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 0
To update
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1.1.0.1 proteomics_improviser Visualisation of PepXML files 0
To update
0.2.0 bg_protein_properties Calculation of various properties from given protein sequences 684
biopython
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0.9 eden_protease_prediction This tool can learn the cleavage specificity of a given class of proteases. 160
eden
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0.1 plotly_regression_performance_plots performance plots for regression problems 1698
python
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0.2 plotly_parallel_coordinates_plot parallel coordinates plot produced with plotly 2002
python
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0.4 plotly_ml_performance_plots performance plots for machine learning problems 3661
galaxy-ml
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0.0.11 bg_platypus efficient and accurate variant-detection in high-throughput sequencing data 0
platypus
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1.2.1.0 piranha Piranha is a peak-caller for CLIP- and RIP-Seq data 2094
piranha
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pharmcat Pharmacogenomics Clinical Annotation Tool 432
To update
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pg_dump pg_import pg_query tool suite for dealing with Postgresql databases from Galaxy's history 0
postgresql
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1.6 pfamscan Search a FASTA sequence against a library of Pfam HMM. Sequence analysis Protein sequence analysis 2047
pfam_scan
Up-to-date
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5.11.0 stats_perf_tool suitable for boolean classification problems 0
perf
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0.2.0+galaxy1 peakachu PEAKachu is a peak-caller for CLIP- and RIP-Seq data 3490
peakachu
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0.1 pandas_rolling_window Rolling window calculations 350
numpy
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2.1.0 AccurateMassSearch AdditiveSeries BaselineFilter CVInspector CompNovo CompNovoCID ConsensusID ConsensusMapNormalizer ConvertTSVToTraML ConvertTraMLToTSV DTAExtractor DeMeanderize Decharger DecoyDatabase Digestor DigestorMotif EICExtractor ERPairFinder ExternalCalibration FFEval FalseDiscoveryRate FeatureFinderCentroided FeatureFinderIdentification FeatureFinderIsotopeWavelet FeatureFinderMRM FeatureFinderMetabo FeatureFinderMultiplex FeatureFinderSuperHirn FeatureLinkerLabeled FeatureLinkerUnlabeled FeatureLinkerUnlabeledQT FidoAdapter FileConverter FileFilter FileInfo FileMerger FuzzyDiff HighResPrecursorMassCorrector IDConflictResolver IDDecoyProbability IDExtractor IDFileConverter IDFilter IDMapper IDMassAccuracy IDMerger IDPosteriorErrorProbability IDRTCalibration IDRipper IDScoreSwitcher IDSplitter ITRAQAnalyzer InclusionExclusionListCreator InspectAdapter InternalCalibration IsobaricAnalyzer LabeledEval LowMemPeakPickerHiRes LowMemPeakPickerHiRes_RandomAccess LuciphorAdapter MRMMapper MRMPairFinder MRMTransitionGroupPicker MSGFPlusAdapter MSSimulator MapAlignmentEvaluation MapNormalizer MapRTTransformer MapStatistics MascotAdapter MascotAdapterOnline MassCalculator MassTraceExtractor MetaProSIP MetaboliteSpectralMatcher MultiplexResolver MzMLSplitter MzTabExporter NoiseFilterGaussian NoiseFilterSGolay OpenSwathAnalyzer OpenSwathAssayGenerator OpenSwathChromatogramExtractor OpenSwathConfidenceScoring OpenSwathDIAPreScoring OpenSwathDecoyGenerator OpenSwathFeatureXMLToTSV OpenSwathFileSplitter OpenSwathMzMLFileCacher OpenSwathRTNormalizer OpenSwathRewriteToFeatureXML OpenSwathWorkflow PTModel PTPredict PeakPickerHiRes PeakPickerIterative PeakPickerWavelet PepNovoAdapter PeptideIndexer PhosphoScoring PrecursorIonSelector PrecursorMassCorrector ProteinInference ProteinQuantifier ProteinResolver QCCalculator QCEmbedder QCExporter QCExtractor QCImporter QCMerger QCShrinker RNPxl RNPxlXICFilter RTEvaluation RTModel RTPredict SemanticValidator SequenceCoverageCalculator SimpleSearchEngine SpecLibCreator SpectraFilterBernNorm SpectraFilterMarkerMower SpectraFilterNLargest SpectraFilterNormalizer SpectraFilterParentPeakMower SpectraFilterScaler SpectraFilterSqrtMower SpectraFilterThresholdMower SpectraFilterWindowMower SpectraMerger SvmTheoreticalSpectrumGeneratorTrainer TICCalculator TMTAnalyzer TOFCalibration TextExporter TopPerc TransformationEvaluation XMLValidator XTandemAdapter OpenMS in version 2.1. 114319
openms
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0.9 numeric_clustering Clustering tool for numberic values 488
anaconda
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3.0 Nucleosome Prediction of Nucleosomes Positions on the Genome Structural genomics Nucleic acid sites, features and motifs Prediction and recognition Nucleosome position prediction Sequence analysis 865
nucleosome_prediction
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2.5.0 nextdenovo String graph-based de novo assembler for long reads Sequencing Sequence assembly De-novo assembly Genome assembly 543
nextdenovo
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1.6.0 netboxr netboxr enables automated discovery of biological process modules by network analysis 13
bioconductor-netboxr
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0.14.0 nanopolish_eventalign nanopolish_methylation nanopolish_polya nanopolish_variants Nanopolish software package for signal-level analysis of Oxford Nanopore sequencing data. 12419
nanopolish
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0.1.1 music_construct_eset music_inspect_eset music_manipulate_eset music_compare music_deconvolution Multi-subject Single Cell deconvolution (MuSiC) 6251
music-deconvolution
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3.1.0 mereg_mOTUs_tables motus_profiler Tool for profiling the abundance of microbial taxa. Metagenomics Taxonomic classification 76
motus
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0.2 bg_mol2gspan converter 0
openbabel
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3.2.3 mitohifi Assembly mitogenomes from Pacbio HiFi read. 2551
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0.2.0 minipolish Polishing miniasm assemblies Sequence assembly Sequencing Localised reassembly Read depth analysis 251
minipolish
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0.2.0 minced MinCED - Mining CRISPRs in Environmental Datasets 1972
minced
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1.2.0 mi_clip Identification of binding sites in CLIP-Seq data. 0
Rscript
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1.2 mgnify_seqprep A modifiied vesion of SeqPrep. Made for use with the MGnify pipelines. Genomics Sequence assembly Sequencing Probes and primers Nucleic acid design 1254
To update
UseGalaxy.or1
0.2.6.1 metilene Differential DNA methylation calling 5981
metilene
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0.99.2 methylkit A method for DNA methylation analysis and annotation from high-throughput bisulfite sequencing. 7
bioconductor-methylkit
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0.5.2 pileometh A tool for processing bisulfite sequencing alignments 28578
methyldackel
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0.1.1 methtools_calling r_correlation_matrix methtools_destrand methtools_dmr methtools_filter methtools_plot smooth_running_window methtools_tiling tools for methylation analysis 5461
methtools
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0.9 mavedb_importer data source for MaveDB 10
To update
UseGalaxy.eu1
0.1.1 markitdown Convert documents to Markdown using markitdown 0
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UseGalaxy.eu1
7.526 rbc_mafft_add rbc_mafft Multiple alignment program for amino acid or nucleotide sequences Sequence analysis Multiple sequence alignment 345522
mafft
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1.101.0 llm_hub LiteLLM - Call all LLM APIs using the OpenAI format. 0
python
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1.0 lighter Lighter is a kmer-based error correction method for whole genome sequencing data Sequencing Whole genome sequencing DNA Genomics k-mer counting Sequence read processing Sequencing quality control Sequencing error detection 180
lighter
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1.0.5.0 bg_labels remaps and annotates alignments 0
labels
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0.0.1 run_jupyter_job Run jupyter notebook script in Galaxy 33
To update
2.17.0 jbrowse2 JBrowse2 Genome Browser integrated as a Galaxy Tool Mapping Structural variation Genomics Gene structure Sequence assembly Genome visualisation Structure visualisation Pathway visualisation 2924
jbrowse2
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1.1.3 itsx ITSx is an open source software utility to extract the highly variable ITS1 and ITS2 subregions from ITS sequences. Functional, regulatory and non-coding RNA Microbiology Sequence feature detection 2235
itsx
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Interproscan queries the interpro database and provides annotations. 0
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0.1.6 instagraal Large genome reassembly based on Hi-C data Sequence assembly Mapping Metagenomics Statistics and probability DNA binding sites Genome assembly Mapping assembly Genetic mapping Scaffolding 159
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8.3.0 json2yolosegment yolo_predict yolo_training tools for building yolo workflows. 0
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1.6.1 woundhealing_scratch_assay Tool to automate quantification of wound healing in high-throughput microscopy scratch assays 31
fiji-morpholibj
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7.1.2-2 imagemagick_image_compare imagemagick_image_convert imagemagick_image_montage Contains tools based on ImageMagick 0
imagemagick
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20240614 imagej2_adjust_threshold_binary imagej2_analyze_particles_binary imagej2_analyze_skeleton imagej2_binary_to_edm imagej2_bunwarpj_adapt_transform imagej2_bunwarpj_align imagej2_bunwarpj_compare_elastic imagej2_bunwarpj_compare_elastic_raw imagej2_bunwarpj_compare_raw imagej2_bunwarpj_compose_elastic imagej2_bunwarpj_compose_raw imagej2_bunwarpj_compose_raw_elastic imagej2_bunwarpj_convert_to_raw imagej2_bunwarpj_elastic_transform imagej2_bunwarpj_raw_transform imagej2_create_image imagej2_crop imagej2_enhance_contrast imagej2_filter imagej2_find_edges imagej2_find_maxima imagej2_make_binary imagej2_math imagej2_noise imagej2_shadows imagej2_sharpen imagej2_skeletonize3d imagej2_smooth imagej2_watershed_binary ImageJ2 is a new version of ImageJ for the next generation of multidimensionalimage data, with a focus on scientific imaging. Imaging Image analysis Image annotation Visualisation 1768
imagej2
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1.3.45 graphicsmagick_image_compare graphicsmagick_image_convert graphicsmagick_image_montage Contains tools based on GraphicsMagick 2806
graphicsmagick
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0.2.0 bia_download Tool to query ftp links for study from bioimage archive 13
wget
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0.1 illumina_methylation_analyser Methylation analyzer for Illumina 450k DNA emthylation microarrays 0
Rscript
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Software for motif discovery and next generation sequencing analysis. 0
To update
0.9.2 hicup2juicer hicup_deduplicator hicup_digester hicup_filter hicup_hicup hicup_mapper hicup_truncater The HiCUP-Pipeline from the Bioinformatics Babraham Institute. 1786
To update
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2.0.2 hictk Convert cooler to juicebox_hic 51
hictk
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0.99 hclust2 Plots heatmaps 0
hclust2
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0.5.2 graphmap_align graphmap_overlap Mapper for long, error-prone reads. Gene transcripts RNA-Seq RNA splicing Sequence trimming EST assembly Read mapping 7528
graphmap
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0.1 graphclust GraphClust can be used for structural clustering of RNA sequences. 6
GraphClust
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0.1.0 graph_converter Convert between different graph formats 0
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1.3.0 rbc_gotohscan Find subsequences in db 72
gotohscan
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GlimmerHMM is a new gene finder based on a Generalized Hidden Markov Model (GHMM) 0
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1.3.11 gfastats Tool for generating sequence statistics and simultaneous genome assembly file manipulation. Computational biology Data handling 26115
gfastats
Up-to-date
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0.2.0 format_metaphlan2_output Format MetaPhlAn2 output to extract abundance at different taxonomic levels Taxonomy Metagenomics Formatting 6878
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1.0.0+galaxy1 format_cd_hit_output Format CD-hit output to rename representative sequences with cluster name and/or extract distribution inside clusters given a mapping file 244
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1.0.0 footprint Find transcription factor footprints 57
footprint
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2.9.6 flye Assembly of long and error-prone reads. Sequence assembly Metagenomics Whole genome sequencing Genomics Genome assembly De-novo assembly Mapping assembly Cross-assembly 76300
flye
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2024 black_forest_labs_flux Using the black forest labs FLUX.1 models to generate image based on user input. 99
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0.2.20 flexynesis flexynesis_cbioportal_import flexynesis_plot flexynesis_utils This is a deep-learning based multi-omics bulk sequencing data integration suite with a focus on (pre-)clinical endpoint prediction. 13
flexynesis
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0.3 bg_find_subsequences 4400
biopython
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0.4 bg_uniq This tool returns all unique lines from a tab-separated file. 9247
python
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0.1.0 ffmpeg_converter A complete, cross-platform solution to record, convert and stream audio and video. 0
ffmpeg
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0.25.1 fastq_info FASTQ info allows to validate single or paired fastq files 23549
fastq_utils
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@VERSION_STRING@ epicseg_segment EpiCSeg is a tool for conducting chromatin segmentation. 255
epicseg
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edta The EDTA package was designed to filter out false discoveries in raw TE candidates and generate a high-quality non-redundant TE library for whole-genome TE annotations. Workflows Mobile genetic elements Plant biology Transcription factors and regulatory sites Model organisms De-novo assembly Deisotoping Genome annotation 4601
edta
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24.10.15 make_ear A tool to compile assembly reports and stastics from assembly pipeline 83
reportlab
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Diffbind provides functions for processing ChIP-Seq data. 0
To update
3.10 diff GNU diff tool that calculates the differences between two files. 441
diffutils
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1.2.0 crispr_recognition_tool CRISPR Recognition Tool 4491
crisper_recognition_tool
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3.0.5 cpat Coding-potential assessment tool using an alignment-free logistic regression model. 699
cpat
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0.2.0 compare_humann2_output Compare outputs of HUMAnN2 for several samples and extract similar and specific information Metagenomics Gene and protein families Comparison 332
To update
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0.3.0 combine_metaphlan_humann Combine MetaPhlAn2 and HUMAnN2 outputs to relate genus/species abundances and gene families/pathways abundances Metagenomics Molecular interactions, pathways and networks Aggregation 643
python
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2.7.1 cleanlab_issue_handler CleanLab is a package to find various types of issues in a dataset. 0
cleanlab
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1.1.9.0 circexplorer A combined strategy to identify circular RNAs (circRNAs and ciRNAs) 526
circexplorer
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1.32.0 chipseeker A tool for ChIP peak annotation and visualization 63025
bioconductor-chipseeker
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2024 chatgpt_openai_api Using the OpenAI GPT models to generate text based on user input. 546
python
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4.2.8 cp_cellprofiler4 cellProfiler4 wrapper 55
To update
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cp_cellprofiler cp_color_to_gray cp_convert_objects_to_image cp_display_data_on_image cp_enhance_or_suppress_features cp_export_to_spreadsheet cp_gray_to_color cp_identify_primary_objects cp_image_math cp_mask_image cp_measure_granularity cp_measure_image_area_occupied cp_measure_image_intensity cp_measure_image_quality cp_measure_object_intensity cp_measure_object_size_shape cp_measure_texture cp_overlay_outlines cp_relate_objects cp_save_images cp_common cp_tile cp_track_objects cellProfiler wrapper Imaging Microarray experiment Genotype and phenotype Quantification Image analysis Parsing 11862
cellprofiler
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3.1.0 cellpose Cellpose is an anatomical segmentation algorithm 22
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2.3 canu Canu is a hierarchical assembly pipeline designed for high-noise single-molecule sequencing (such as the PacBio RS II/Sequel or Oxford Nanopore MinION). Genomics De-novo assembly 19904
canu
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0.1.2 blockbuster Blockbuster detects blocks of overlapping reads using a gaussian-distribution approach. 3384
blockbuster
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4.0.7 blobtoolkit Identification and isolation non-target data in draft and publicly available genome assemblies. Sequence assembly Model organisms Workflows Phylogenomics Zoology Biodiversity Genome assembly Scaffolding Visualisation Data deposition Data parsing 2663
To update
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0.22.1 bismark_pretty_report bismark_bowtie2 bismark_deduplicate bismark_methylation_extractor A tool to map bisulfite converted sequence reads and determine cytosine methylation states 17626
bismark
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3.7.0 bionano_scaffold Bionano Solve is a set of tools for analyzing Bionano data 1435
To update
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1.1 biomodels_biomd0000001066 biomodels_biomd0000001076 Wrappers for tools to bring BioModels AI models into Galaxy. 113
To update
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2.4.1 bioimage_inference Load model from BioImage.IO and make inferences Machine learning Computer science 59
python
pytorch
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0.1.0 bigwig_to_bedgraph Convert from bigWig to bedGraph format 7955
ucsc_tools
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0.1.0 barcode_collapse Paired End randomer aware duplicate removal algorithm 0
pysam
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1.1 bamhash Hash BAM and FASTQ files to verify data integrity 188
bamhash
Up-to-date
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0.1.6 atactk_trim_adapters Trim adapters from paired-end HTS reads. 291
atactk
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6.1.1 antismash Antismash allows the genome-wide identification, annotation and analysis of secondary metabolite biosynthesis gene clusters Molecular interactions, pathways and networks Gene and protein families Sequence clustering Gene prediction Differential gene expression analysis 40761
antismash
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1.4.0 agat GTF/GFF analysis toolkit Genomics Data handling Genome annotation 6371
agat
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0.4 structure_to_gspan Convert RNA structure to GSPAN graphs 3074
graphclust-wrappers
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0.5 preproc Preprocessing input for GraphClust 1921
graphclust-wrappers
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0.4 preMloc This tool prepares files for locarna step. 2140
graphclust-wrappers
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0.4 motifFinderPlot Plotting results for GraphClust 71
seaborn
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9.2.3.1 NSPDK_candidateClust nspdk_sparse Produces an explicit sparse feature encoding and copmutes global feature index and returns top dense sets. 62905
graphclust-wrappers
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0.4 locarna_best_subtree MLocARNA computes a multiple sequence-structure alignment of RNA sequences. 50825
graphclust-wrappers
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0.4 gspan Second step of GraphClust 161
graphclust-wrappers
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0.5 graphclust_glob_report_no_align Redundant GraphClust clusters are merged and instances that belong to multiple clusters are assigned unambiguously. 108
graphclust-wrappers
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0.5 glob_report Post-processing. Redundant clusters are merged and instances that belong to multiple clusters are assigned unambiguously. For every pair of clusters, the relative overlap (i.e. the fraction of instances that occur in both clusters) is computed and clusters are merged if the overlap exceeds 50%. instances that occur in both clusters) is computed and clusters are merged if the overlap exceeds 50%. 2131
graphclust-wrappers
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0.4 cmFinder Determines consensus motives for sequences. 50693
graphclust-wrappers
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0.1 graphclust_align_cluster Align predicted clusters of glob_report_no_align step with locarna and conservation analysis and visualizations. 3101
graphclust-wrappers
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0.6.0 graphclust_aggregate_alignments Aggregate and filter alignment metrics of individual clusters, like the output of graphclust_align_cluster. 120
graphclust-wrappers
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1.4.1 10x_bamtofastq Converts 10x Genomics BAM to FASTQ 367
10x_bamtofastq
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0.1 vcftools_subset Select samples from a VCF dataset 286
tabix
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0.1 vcftools_slice Subset VCF dataset by genomic regions 8748
echo
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0.1.11 vcftools_merge Merge multiple VCF datasets into a single dataset 1738
tabix
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0.1.1 vcftools_isec Intersect multiple VCF datasets 1071
tabix
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0.1.11 vcftools_consensus Apply VCF variants to a fasta file to create consensus sequence 0
samtools
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0.1 vcftools_compare Compare VCF files to get overlap and uniqueness statistics 653
tabix
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0.1 vcftools_annotate Annotate VCF using custom/user-defined annotations 4583
echo
To update
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1.0.0 t2t_report Summarize taxonomy 8154
taxonomy
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1.0.0 Draw_phylogram Draw phylogeny Phylogenomics Phylogenetic tree visualisation 8430
taxonomy
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1.0.0 poisson2test Poisson two-sample test 1072
taxonomy
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1.0.1 lca1 Find lowest diagnostic rank 6273
taxonomy
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1.2+galaxy0 Kraken2Tax Convert Kraken output to Galaxy taxonomy data. 68046
gawk
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1.1.1 Fetch Taxonomic Ranks Fetch taxonomic representation Taxonomy Database search ID mapping 14747
taxonomy
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1.0.0 find_diag_hits Find diagnostic hits 1857
taxonomy
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1.0.1 hgv_snpFreq snpFreq significant SNPs in case-control data 980
R
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1.0.0 hgv_hilbertvis HVIS visualization of genomic data with the Hilbert curve 265
R
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1.0.0 hgv_funDo FunDO human genes associated with disease terms 1794
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1.0.0 tables_arithmetic_operations Arithmetic Operations on tables 2310
perl
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0.1 subtract_query1 Subtract Whole Dataset from another dataset 43295
bx-python
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1.0.0 gops_subtract_1 Subtract the intervals of two datasets 775082
bx-python
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1.0.0 gops_merge_1 Merge the overlapping intervals of a dataset 697093
bx-python
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1.0.0 gops_join_1 Join the intervals of two datasets side-by-side 848340
bx-python
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1.0.0 gops_intersect_1 Intersect the intervals of two datasets 1142164
bx-python
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1.0.0 get_flanks1 Get flanks returns flanking region/s for every gene 568957
bx-python
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4.0.1 flanking_features_1 Fetch closest non-overlapping feature for every interval 35163
bx-python
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1.0.0 gops_coverage_1 Coverage of a set of intervals on second set of intervals 46481
bx-python
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1.0.1 gops_concat_1 Concatenate two bed files 683959
bx-python
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1.0.0 gops_complement_1 Complement intervals of a dataset 5536
bx-python
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1.0.0 gops_cluster_1 Cluster the intervals of a dataset 32992
bx-python
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1.0.0 gops_basecoverage_1 Base Coverage of all intervals 46501
bx-python
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1.0.2 XY_Plot_1 Plotting tool for multiple series and graph types 25190
r-base
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1.0.1 winSplitter Make windows 3974
bx-python
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1.0.1 wtavg Assign weighted-average of the values of features overlapping an interval 2308
galaxy-ops
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1.0.0 vcf_intersect Generate the intersection of two VCF files 482
To update
1.0.0 vcf_filter Filter a VCF file 1146
To update
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1.0.0 vcf_extract Extract reads from a specified region 569
To update
1.0.0 vcf_annotate Annotate a VCF file (dbSNP, hapmap) 342
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1.0.0 vcf2pgSnp VCF to pgSnp 2966
To update
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2.4.2 varscan VarScan wrapper 66251
varscan
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1.0.1 build_ucsc_custom_track_1 Build custom track for UCSC genome browser 19391
python
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0.0.1 trimmer Trim leading or trailing characters. 118310
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0.1 tophat_fusion_post Wrapper for Tophat-Fusion post step 1183
blast+
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2.1.1 tophat2 Tophat - fast splice junction mapper for RNA-Seq reads 388052
bowtie2
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1.5.0 tophat Tophat for Illumina 66525
samtools
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1.1.1 tab2fasta Tabular-to-FASTA 627706
python
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0.2 table_annovar Annotate a VCF file using ANNOVAR annotations to produce a tabular file that can be filtered 64533
annovar
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1.0.1 t_test_two_samples T Test for Two Samples 2659
R
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1.0.1 substitutions1 Fetch substitutions from pairwise alignments 901
bx-python
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UseGalaxy.or1
1.0.0 subRate1 Estimate substitution rates for non-coding regions 4015
To update
1.0.0 split_paired_reads Split paired end reads 397
To update
1.1 peakcalling_sicer Statistical approach for the Identification of ChIP-Enriched Regions 10212
SICER
Up-to-date
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1.0.0 Show tail1 Select lines from the end of a file. 28184
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1.0.0 Show beginning1 Select lines from the beginning of a file. 181555
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1.0.0 trim_reads Select high quality segments 6877
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1.0.2 quality_score_distribution Build base quality distribution 3523
fontconfig
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1.0.0 hist_high_quality_score Histogram of high quality score reads 0
rpy
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1.0.3 scatterplot_rpy Scatterplot of two numeric columns 11290
numpy
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1.0.1 sam_bw_filter Filter SAM on bitwise flag values 76717
python
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1.0.2 sam2interval Convert SAM to interval. 20365
python
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1.0.0 rmapq_wrapper RMAPQ for Solexa Short Reads Alignment with Quality Scores 0
rmap
To update
1.0.0 rmap_wrapper RMAP for Solexa Short Reads Alignment 0
rmap
To update
1.0.0 Remove beginning1 Remove lines from the beginning of a file. 353254
To update
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1.0.0 rcve1 Compute RCVE 193
R
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1.0.1 qualityFilter Filter nucleotides based on quality scores 724
bx-python
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1.0.2 pca1 Principal Component Analysis 18278
rpy
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1.0.1 plot_for_lda_output1 Draw ROC plot on "Perform LDA" output 1138
R
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1.0.2 pileup_parser Filter pileup on coverage and SNPs 59527
perl
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1.0.3 pileup_interval Pileup-to-Interval condenses pileup format into ranges of bases 9393
bx-python
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1.0.0 pgSnp2gd_snp Convert from pgSnp to gd_snp 0
To update
1.0.0 Pearson_and_apos_Correlation1 Pearson and apos Correlation between any two numeric columns 2
To update
1.0.0 partialRsq Compute partial R square 142
R
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1.0.0 mutate_snp_codon_1 Mutate Codons with SNPs 472
To update
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1.0.0 multispecies_orthologous_microsats Extract orthologous microsatellites 0
bx-sputnik
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0.0.1 maximal_information_based_nonparametric_exploration Maximal Information-based Nonparametric Exploration 75
MINE
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1.1.0 microsats_mutability1 Estimate microsatellite mutability by specified attributes 315
bx-python
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1.0.0 microsats_align1 Extract Orthologous Microsatellites from pair-wise alignments 978
sputnik
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1.0.0 microsatellite_birthdeath Identify microsatellite births and deaths 0
To update
1.0.3 mergeCols1 Merge columns together. 171104
python
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1.0.1 megablast_xml_parser Parse blast XML output 4377
python
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1.0.0 mapToUCSC Format mapping data as UCSC custom track 0
To update
1.0.0 cpgFilter Mask CpG/non-CpG sites from MAF file 356
bx-python
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1.0.1 LogisticRegression Perform Logistic Regression with vif 173
numpy
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1.0.1 LinearRegression1 Perform Linear Regression 1131
R
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1.0.1 lda_analy1 Perform Linear Discriminant Analysis 1755
R
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1.1.1 lastz_paired_reads_wrapper Galaxy wrapper for the Lastz alignment tool on paired reads 19
lastz
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1.0.0 kpca1 Kernel Principal Component Analysis 883
rpy
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1.0.0 kcca1 Kernel Canonical Correlation Analysis 422
rpy
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1.0.3 indels_3way Fetch Indels from 3-way alignments 314
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1.0.5 histogram_rpy Histogram of a numeric column 55379
rpy2
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1.0.3 hisat HISAT is a fast and sensitive spliced alignment program. 228
hisat
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2.0.1 gmaj_1 GMAJ Multiple Alignment Viewer 1008
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1.0.0 getIndels_2way Fetch Indels from pairwise alignments 237
numpy
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1.0.0 indelRates_3way Estimate Indel Rates for 3-way alignments 291
bx-python
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1.0.0 generate_matrix_for_pca_and_lda1 Generate a Matrix for using PC and LDA 1419
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0.1 filter_combined_via_tracking Filter Combined Transcripts 664
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2.0.0 featureCoverage1 Feature coverage 36100
bx-python
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1.0.0 fastqsolexa_to_fasta_qual FASTQSOLEXA-to-FASTA-QUAL extracts sequences and quality scores from FASTQSOLEXA data 8
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1.1.5 fastq_quality_trimmer FASTQ Quality Trimmer by sliding window 111169
galaxy_sequence_utils
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1.1.1 fasta2tab FASTA-to-Tabular converter 330253
python
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1.2 fasta_filter_by_length Filter sequences by length 172303
python
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0.0.1 fasta_concatenate0 Concatenate FASTA alignment by species 63569
bx-python
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1.0.4 fasta_compute_length Compute sequence length 69533
python
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1.1.1 express Quantify the abundances of a set of target sequences from sampled subsequences 4425
eXpress
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1.0.2 dwt_var1 Wavelet variance using Discrete Wavelet Transfoms 290
r-bitops
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1.0.1 compute_p-values_max_variances_feature_occurrences_in_one_dataset_using_discrete_wavelet_transfom Compute P-values and Max Variances for Feature Occurrences 153
r-waveslim
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1.0.1 compute_p-values_second_moments_feature_occurrences_between_two_datasets_using_discrete_wavelet_transfom Compute P-values and Second Moments for Feature Occurrences 144
r-waveslim
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1.0.1 compute_p-values_correlation_coefficients_featureA_featureB_occurrences_between_two_datasets_using_discrete_wavelet_transfom Compute P-values and Correlation Coefficients for Occurrences of Two Set of Features 145
r-waveslim
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1.0.1 compute_p-values_correlation_coefficients_feature_occurrences_between_two_datasets_using_discrete_wavelet_transfom Compute P-values and Correlation Coefficients for Feature Occurrences 162
r-waveslim
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1.0.0 draw_stacked_barplots Draw Stacked Bar Plots for different categories and different criteria 469
R
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1.0.0 dividePgSnp Separate pgSnp alleles into columns 212
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0.1 dgidb_annotate Annotates a tabular file with information from the Drug-Gene Interaction Database (http://dgidb.genome.wustl.edu/) 373
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1.0.0 delete_overlapping_indels Delete Overlapping Indels from a chromosome indels file 40
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1.0.2 Cut1 Select columns from a dataset. 3047543
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1.0.1 cummerbund_to_cuffdiff Regenerate the tabular files generated by cuffdiff from a cummeRbund SQLite database. 3899
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2.16.0 cummeRbund Wrapper for the Bioconductor cummeRbund library 20572
fonts-conda-ecosystem
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1.0.0 ctdBatch_1 CTD analysis of chemicals, diseases, or genes 666
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0.2 count_gff_features Count GFF Features 2351
galaxy-ops
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1.0.0 cor2 Correlation for numeric columns 6747
rpy
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1.0.0 color2nuc Convert Color Space to Nucleotides 0
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1.0.1 Convert characters1 Convert delimiters to tab. 204876
python
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1.0.0 Condense characters1 Condense consecutive characters. 2413
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1.0.1 compute_q_values Compute q-values based on multiple simultaneous tests p-values 35
R
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1.0.0 compute_motifs_frequency Compute Motif Frequencies in indel flanking regions. 442
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1.0.0 compute_motif_frequencies_for_all_motifs Compute Motif Frequencies For All Motifs, motif by motif. 474
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1.0.1 ChangeCase Convert column case. 33846
perl
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0.0.1 cd_hit_dup simple tool for removing duplicates from sequencing reads 7789
cd-hit-auxtools
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0.0.2 peakcalling_ccat Control-based ChIP-seq Analysis Tool 179
ccat
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1.0.0 categorize_elements_satisfying_criteria Categorize Elements satisfying criteria. 249
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1.0.0 cca1 Canonical Correlation Analysis 582
R
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1.2.0 bowtie_wrapper Galaxy wrappers for the Bowtie short read mapping tools. 248551
bowtie
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1.0.0 blat2wig Coverage of the Reads in wiggle format 0
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1.0.0 generate_coverage_report Polymorphism of the Reads 0
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1.0.0 BestSubsetsRegression1 Perform Best-subsets Regression 260
numpy
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1.0.1 addValue Add a value as a new column. 689289
perl
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0
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2025.7.0+dist.h44bd78f6 qiime2_core__tools__export qiime2_core__tools__import qiime2_core__tools__import_fastq Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 95748
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2025.7.0+q2galaxy.2025.7.0 qiime2__vsearch__cluster_features_closed_reference qiime2__vsearch__cluster_features_de_novo qiime2__vsearch__cluster_features_open_reference qiime2__vsearch__dereplicate_sequences qiime2__vsearch__fastq_stats qiime2__vsearch__merge_pairs qiime2__vsearch__uchime_denovo qiime2__vsearch__uchime_ref Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 451
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0.0.1.dev0+q2galaxy.2025.7.0 qiime2__vizard__boxplot qiime2__vizard__heatmap qiime2__vizard__lineplot qiime2__vizard__scatterplot_2d Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 3
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2025.7.0+q2galaxy.2025.7.0 qiime2__taxa__barplot qiime2__taxa__collapse qiime2__taxa__filter_seqs qiime2__taxa__filter_table Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 2528
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2025.7.0+q2galaxy.2025.7.0 qiime2__stats__alpha_group_significance qiime2__stats__collate_stats qiime2__stats__facet_across qiime2__stats__facet_within qiime2__stats__mann_whitney_u qiime2__stats__mann_whitney_u_facet qiime2__stats__plot_rainclouds qiime2__stats__prep_alpha_distribution qiime2__stats__wilcoxon_srt qiime2__stats__wilcoxon_srt_facet Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 0
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2025.7.0+q2galaxy.2025.7.0 qiime2__sample_classifier__classify_samples qiime2__sample_classifier__classify_samples_from_dist qiime2__sample_classifier__classify_samples_ncv qiime2__sample_classifier__confusion_matrix qiime2__sample_classifier__fit_classifier qiime2__sample_classifier__fit_regressor qiime2__sample_classifier__heatmap qiime2__sample_classifier__metatable qiime2__sample_classifier__predict_classification qiime2__sample_classifier__predict_regression qiime2__sample_classifier__regress_samples qiime2__sample_classifier__regress_samples_ncv qiime2__sample_classifier__scatterplot qiime2__sample_classifier__split_table qiime2__sample_classifier__summarize Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 64
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2025.7.0+q2galaxy.2025.7.0 qiime2__rescript__cull_seqs qiime2__rescript__degap_seqs qiime2__rescript__dereplicate qiime2__rescript__edit_taxonomy qiime2__rescript__evaluate_classifications qiime2__rescript__evaluate_cross_validate qiime2__rescript__evaluate_fit_classifier qiime2__rescript__evaluate_seqs qiime2__rescript__evaluate_taxonomy qiime2__rescript__extract_seq_segments qiime2__rescript__filter_seqs_length qiime2__rescript__filter_seqs_length_by_taxon qiime2__rescript__filter_taxa qiime2__rescript__get_bv_brc_genome_features qiime2__rescript__get_bv_brc_genomes qiime2__rescript__get_bv_brc_metadata qiime2__rescript__get_gtdb_data qiime2__rescript__get_midori2_data qiime2__rescript__get_ncbi_data qiime2__rescript__get_ncbi_data_protein qiime2__rescript__get_ncbi_genomes qiime2__rescript__get_pr2_data qiime2__rescript__get_silva_data qiime2__rescript__get_unite_data qiime2__rescript__merge_taxa qiime2__rescript__orient_reads qiime2__rescript__orient_seqs qiime2__rescript__parse_silva_taxonomy qiime2__rescript__reverse_transcribe qiime2__rescript__subsample_fasta qiime2__rescript__trim_alignment Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 7
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UseGalaxy.eu3
2025.7.0+q2galaxy.2025.7.0 qiime2__quality_filter__q_score Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 147
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UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
2025.7.0+q2galaxy.2025.7.0 qiime2__quality_control__bowtie2_build qiime2__quality_control__decontam_identify qiime2__quality_control__decontam_identify_batches qiime2__quality_control__decontam_score_viz qiime2__quality_control__evaluate_composition qiime2__quality_control__evaluate_seqs qiime2__quality_control__evaluate_taxonomy qiime2__quality_control__exclude_seqs qiime2__quality_control__filter_reads Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 104
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UseGalaxy.cz6 UseGalaxy.eu6 UseGalaxy.fr6 UseGalaxy.or6
2025.7.0+q2galaxy.2025.7.0 qiime2__phylogeny__align_to_tree_mafft_fasttree qiime2__phylogeny__align_to_tree_mafft_iqtree qiime2__phylogeny__align_to_tree_mafft_raxml qiime2__phylogeny__fasttree qiime2__phylogeny__filter_table qiime2__phylogeny__filter_tree qiime2__phylogeny__iqtree qiime2__phylogeny__iqtree_ultrafast_bootstrap qiime2__phylogeny__midpoint_root qiime2__phylogeny__raxml qiime2__phylogeny__raxml_rapid_bootstrap qiime2__phylogeny__robinson_foulds Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 1068
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UseGalaxy.cz12 UseGalaxy.eu12 UseGalaxy.fr12 UseGalaxy.or12
2025.7.0+q2galaxy.2025.7.0 qiime2__metadata__distance_matrix qiime2__metadata__merge qiime2__metadata__shuffle_groups qiime2__metadata__tabulate Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 2512
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2025.7.0+q2galaxy.2025.7.0 qiime2__longitudinal__anova qiime2__longitudinal__feature_volatility qiime2__longitudinal__first_differences qiime2__longitudinal__first_distances qiime2__longitudinal__linear_mixed_effects qiime2__longitudinal__maturity_index qiime2__longitudinal__nmit qiime2__longitudinal__pairwise_differences qiime2__longitudinal__pairwise_distances qiime2__longitudinal__plot_feature_volatility qiime2__longitudinal__volatility Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 209
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2025.7.0+q2galaxy.2025.7.0 qiime2__fragment_insertion__classify_otus_experimental qiime2__fragment_insertion__filter_features qiime2__fragment_insertion__sepp Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 104
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UseGalaxy.cz3 UseGalaxy.eu3 UseGalaxy.fr3 UseGalaxy.or3
2025.7.0+q2galaxy.2025.7.0 qiime2__feature_table__core_features qiime2__feature_table__filter_features qiime2__feature_table__filter_features_conditionally qiime2__feature_table__filter_samples qiime2__feature_table__filter_seqs qiime2__feature_table__group qiime2__feature_table__heatmap qiime2__feature_table__merge qiime2__feature_table__merge_seqs qiime2__feature_table__merge_taxa qiime2__feature_table__normalize qiime2__feature_table__presence_absence qiime2__feature_table__rarefy qiime2__feature_table__relative_frequency qiime2__feature_table__rename_ids qiime2__feature_table__split qiime2__feature_table__subsample_ids qiime2__feature_table__summarize qiime2__feature_table__summarize_plus qiime2__feature_table__tabulate_feature_frequencies qiime2__feature_table__tabulate_sample_frequencies qiime2__feature_table__tabulate_seqs qiime2__feature_table__transpose Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 5627
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UseGalaxy.cz17 UseGalaxy.eu17 UseGalaxy.fr17 UseGalaxy.or17
2025.7.0+q2galaxy.2025.7.0 qiime2__feature_classifier__blast qiime2__feature_classifier__classify_consensus_blast qiime2__feature_classifier__classify_consensus_vsearch qiime2__feature_classifier__classify_hybrid_vsearch_sklearn qiime2__feature_classifier__classify_sklearn qiime2__feature_classifier__extract_reads qiime2__feature_classifier__find_consensus_annotation qiime2__feature_classifier__fit_classifier_naive_bayes qiime2__feature_classifier__fit_classifier_sklearn qiime2__feature_classifier__makeblastdb qiime2__feature_classifier__vsearch_global Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 3350
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UseGalaxy.cz10 UseGalaxy.eu10 UseGalaxy.fr10 UseGalaxy.or10
2025.7.0+q2galaxy.2025.7.0 qiime2__emperor__biplot qiime2__emperor__plot qiime2__emperor__procrustes_plot Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 380
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UseGalaxy.cz3 UseGalaxy.eu3 UseGalaxy.fr3 UseGalaxy.or3
2025.7.0+q2galaxy.2025.7.0 qiime2__diversity_lib__alpha_passthrough qiime2__diversity_lib__beta_passthrough qiime2__diversity_lib__beta_phylogenetic_meta_passthrough qiime2__diversity_lib__beta_phylogenetic_passthrough qiime2__diversity_lib__bray_curtis qiime2__diversity_lib__faith_pd qiime2__diversity_lib__jaccard qiime2__diversity_lib__observed_features qiime2__diversity_lib__pielou_evenness qiime2__diversity_lib__shannon_entropy qiime2__diversity_lib__unweighted_unifrac qiime2__diversity_lib__weighted_unifrac Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 2095
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UseGalaxy.cz12 UseGalaxy.eu12 UseGalaxy.fr12 UseGalaxy.or12
2025.7.0+q2galaxy.2025.7.0 qiime2__diversity__adonis qiime2__diversity__alpha qiime2__diversity__alpha_correlation qiime2__diversity__alpha_group_significance qiime2__diversity__alpha_phylogenetic qiime2__diversity__alpha_rarefaction qiime2__diversity__beta qiime2__diversity__beta_correlation qiime2__diversity__beta_group_significance qiime2__diversity__beta_phylogenetic qiime2__diversity__beta_rarefaction qiime2__diversity__bioenv qiime2__diversity__core_metrics qiime2__diversity__core_metrics_phylogenetic qiime2__diversity__filter_alpha_diversity qiime2__diversity__filter_distance_matrix qiime2__diversity__mantel qiime2__diversity__partial_procrustes qiime2__diversity__pcoa qiime2__diversity__pcoa_biplot qiime2__diversity__procrustes_analysis qiime2__diversity__tsne qiime2__diversity__umap Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 3866
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UseGalaxy.cz21 UseGalaxy.eu22 UseGalaxy.fr21 UseGalaxy.or21
2025.7.0+q2galaxy.2025.7.0 qiime2__demux__emp_paired qiime2__demux__emp_single qiime2__demux__filter_samples qiime2__demux__partition_samples_paired qiime2__demux__partition_samples_single qiime2__demux__subsample_paired qiime2__demux__subsample_single qiime2__demux__summarize qiime2__demux__tabulate_read_counts Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 2279
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UseGalaxy.cz6 UseGalaxy.eu6 UseGalaxy.fr6 UseGalaxy.or6
2025.7.0+q2galaxy.2025.7.0 qiime2__deblur__denoise_16S qiime2__deblur__denoise_other qiime2__deblur__visualize_stats Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 337
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UseGalaxy.cz3 UseGalaxy.eu3 UseGalaxy.fr3 UseGalaxy.or3
2025.7.0+q2galaxy.2025.7.0 qiime2__dada2__denoise_ccs qiime2__dada2__denoise_paired qiime2__dada2__denoise_pyro qiime2__dada2__denoise_single Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 2540
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UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.fr4 UseGalaxy.or4
2025.7.0+q2galaxy.2025.7.0 qiime2__cutadapt__demux_paired qiime2__cutadapt__demux_single qiime2__cutadapt__trim_paired qiime2__cutadapt__trim_single Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 570
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UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.fr4 UseGalaxy.or4
2025.7.0+q2galaxy.2025.7.0 qiime2__composition__add_pseudocount qiime2__composition__ancom qiime2__composition__ancombc qiime2__composition__ancombc2 qiime2__composition__ancombc2_visualizer qiime2__composition__da_barplot qiime2__composition__tabulate Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 822
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UseGalaxy.cz4 UseGalaxy.eu4 UseGalaxy.fr2 UseGalaxy.or4
2025.7.0+q2galaxy.2025.7.0 qiime2__alignment__mafft qiime2__alignment__mafft_add qiime2__alignment__mask Microbial ecology Metatranscriptomics Metagenomics Demultiplexing Visualisation Taxonomic classification 576
To update
UseGalaxy.cz3 UseGalaxy.eu3 UseGalaxy.fr3 UseGalaxy.or3
0.1.2.7 segalign A Scalable GPU System for Pairwise Whole Genome Alignments based on LASTZ's seed-filter-extend paradigm. 379
segalign-galaxy
Up-to-date
UseGalaxy.or1
0.0.7 rdeval rdeval_report rdeval is a General purpose, multithreaded read analysis and manipulation tool. 0
rdeval
Up-to-date
UseGalaxy.or2
0.5.0 ncbi_fcs_adaptor FCS-adaptor detects adaptor and vector contamination in genome sequences. 2155
To update
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0.4.1 ncbi_egapx Eukaryotic Genome Annotation Pipeline - External (EGAPx) 515
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0.1.2.7 kegalign A Scalable GPU System for Pairwise Whole Genome Alignments based on LASTZ's seed-filter-extend paradigm. 138
kegalign-full
Up-to-date
UseGalaxy.or1
1.04.22 batched_lastz Galaxy wrapper for the batching Lastz runs 226
lastz
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0.2-2 ip_wsi_extract_top_view WSI Extract Top View 38
scikit-image
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0.22.0 voronoi_tessellation Compute Voronoi tesselation Imaging Software engineering Literature and language Image analysis Image annotation Visualisation Data handling 61
scikit-image
scikit-image
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0.5-2 ip_visceral_evaluatesegmentation Visceral Project - Evaluate Segmentation Tool 25
visceral-evaluatesegmentation
evaluatesegmentation-tool
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6.0 unzip Unzip file 10418
unzip
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0.2.0 ip_superdsm Globally optimal segmentation method based on superadditivity and deformable shape models for cell nuclei in fluorescence microscopy images Image analysis 26
superdsm
superdsm
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0.1 ip_spot_detection_2d Spot detection in 2D image sequence Imaging Bioinformatics Image analysis 79
giatools
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0.2-3 ip_split_labelmap Split Labelmaps Imaging Bioinformatics Image analysis 51
scikit-image
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2.2.3 ip_split_image Split image along axes 0
numpy
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0.3-4 ip_slice_image Slice image Imaging Bioinformatics Image analysis 127
scikit-image
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1.4 ip_segmetrics Image segmentation and object detection performance measures Image analysis 10
segmetrics
segmetrics
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0.18.3 ip_scale_image Scale image Imaging Software engineering Literature and language Image analysis Image annotation Visualisation Data handling 521
scikit-image
scikit-image
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UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
2023.11.12 rfove Perform segmentation region-based fitting of overlapping ellipses Cell biology Biomedical science Imaging Image analysis 15
To update
UseGalaxy.eu1
1.26.4 repeat_channels Convert single-channel to multi-channel image Imaging Bioinformatics Image analysis 14
numpy
To update
UseGalaxy.eu1
0.1.1 ip_projective_transformation_points Projective transformation of ROIs defined by pixel (point) coordinates Imaging Bioinformatics Image analysis 21445
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.1.2 ip_projective_transformation Projective transformation Imaging Bioinformatics Image analysis 86
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.0.3-2 ip_points_association_nn Association of points in consecutive frames Imaging Bioinformatics Image analysis 46
numpy
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.4.1 ip_points_to_label Points to label image Imaging Bioinformatics Image analysis 54
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.8.1 plantseg Tool for cell instance aware segmentation in densely packed 3D volumetric images Plant biology Bioimaging Light microscopy Machine learning Electron microscopy Network analysis Quantification Microscope image visualisation 0
plant-seg
To update
UseGalaxy.eu1
0.2-2 ip_permutate_axis Permutates axes Imaging Bioinformatics Image analysis 42
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.0.4 ip_overlay_images Overlay two images Imaging Bioinformatics Image analysis 340
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
0.2.0.4 orientationpy Compute image orientation 0
orientationpy
orientationj
Up-to-date
UseGalaxy.eu1
1.12.0 morphological_operations Apply morphological operations to images 0
scipy
scipy
To update
UseGalaxy.eu1
0.3-2 ip_merge_neighbours_in_label Merge Neighbours in Label Image Imaging Bioinformatics Image analysis 25
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.7-2 ip_mahotas_features Compute image features using mahotas. 44
mahotas
mahotas-feature-computation
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.1.0-2 ip_landmark_registration Landmark Registration Imaging Bioinformatics Image analysis 936
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.2-2 ip_labelimage_to_points Label Image to Points Imaging Bioinformatics Image analysis 38
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.26.4 label_to_binary Convert label map to binary image Imaging Bioinformatics Image analysis 0
numpy
To update
UseGalaxy.eu1
0.1-2 imagecoordinates_flipaxis Flip coordinate axes Imaging Bioinformatics Image analysis 21850
pandas
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.0.3-2 ip_image_registration Intensity-based Image Registration Imaging Bioinformatics Image analysis 16
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1
1.26.4 image_math Process images using arithmetic expressions 74
numpy
To update
UseGalaxy.eu1 UseGalaxy.or1
5.7.1 ip_imageinfo Extracts image metadata 847
bftools
python-bioformats
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.3-2 ip_detection_viz Detection Visualization Imaging Bioinformatics Image analysis 49
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.0.3-2 ip_curve_fitting Polynomial curve fitting to data points Imaging Bioinformatics Image analysis 29
numpy
To update
UseGalaxy.cz1 UseGalaxy.eu1
0.4.1 ip_crop_image Crop image 0
giatools
Up-to-date
UseGalaxy.eu1
0.0.5-2 ip_count_objects Count Objects Imaging Bioinformatics Image analysis 503
scikit-image
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.0.4-2 ip_coordinates_of_roi Coordinates of ROI Imaging Bioinformatics Image analysis 16547
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.3-1 ip_concat_channels Concatenate images Imaging Bioinformatics Image analysis 84
scikit-image
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
3.2.1 colorize_labels Colorize label map 62
networkx
To update
UseGalaxy.eu1
0.9 ip_color_deconvolution Color-deconvolution methods Imaging Bioinformatics Image analysis 45
scikit-image
To update
UseGalaxy.eu1 UseGalaxy.no1
0.7.0 bf2raw Convert image to OME-Zarr 62
To update
UseGalaxy.eu1 UseGalaxy.fr1
0.1-2 ip_binaryimage_to_points Binary Image to Points Imaging Bioinformatics Image analysis 29
numpy
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.6 ip_binary_to_labelimage Binary 2 label image Imaging Bioinformatics Image analysis 1689
giatools
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
6.7.0 ip_convertimage Convert image 2118
bftools
python-bioformats
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.24.0 background_removal Background removal filters using scikit-image 30
scikit-image
To update
UseGalaxy.eu1
0.4.0 ip_anisotropic_diffusion Anisotropic image diffusion 41
medpy
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.12.0 ip_filter_standard 2d simple filter 6612
scipy
scipy
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.18.1 ip_histogram_equalization 2d histogram equalization Imaging Software engineering Literature and language Image analysis Image annotation Visualisation Data handling 1071
scikit-image
scikit-image
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.0.1-4 ip_2d_filter_segmentation_by_features filter segmentation by rules Imaging Bioinformatics Image analysis 7015
scikit-image
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.18.1 ip_2d_feature_extraction 2D feature extraction Imaging Software engineering Literature and language Image analysis Image annotation Visualisation Data handling 14027
scikit-image
scikit-image
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.25.0 ip_threshold Automatic thresholding Imaging Software engineering Literature and language Image analysis Image annotation Visualisation Data handling 7277
scikit-image
scikit-image
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.98.2 w4mjoinpn Join positive- and negative-mode W4M datasets 178
coreutils
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.98.19 w4mclassfilter Filter W4M data by values or metadata 4517
r-base
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.98.18 w4mcorcov OPLS-DA Contrasts of Univariate Results 386
r-base
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
analysis_add_analysis analysis_get_analyses analysis_load_blast analysis_load_fasta analysis_load_gff3 analysis_load_go analysis_load_interpro analysis_sync db_index db_populate_mviews entity_publish expression_add_biomaterial expression_add_expression expression_delete_biomaterials expression_get_biomaterials expression_sync_biomaterials feature_delete_orphans feature_sync organism_add_organism organism_get_organisms organism_sync phylogeny_sync Galaxy tools allowing to load data into a remote Tripal server.Tripal is a toolkit for construction of online biological (genetics, genomics, breeding, etc), community database,and is a member of the GMOD family of tools. Tripal provides by default integration with the GMOD Chado database schema and Drupal, a popular Content Management Systems (CMS).https://github.com/galaxy-genome-annotation/python-tripal 0
python-tripal
To update
2.3.8 repeatexplorer_clustering Tool for annotation of repeats from unassembled shotgun reads. 225
To update
UseGalaxy.eu1
jbrowse_to_container A tool allowing to export a JBrowse dataset into a JBrowse docker container 0
python
To update
0.4.18 genenotebook_build Galaxy tools allowing to load data into a GeneNoteBook database.https://genenotebook.github.io 295
genoboo
Up-to-date
UseGalaxy.eu1 UseGalaxy.fr1
analysis_add_analysis analysis_delete_analyses analysis_get_analyses export_export_fasta export_export_gbk export_export_gff3 expression_add_biomaterial expression_add_expression expression_delete_all_biomaterials expression_delete_biomaterials expression_get_biomaterials feature_delete_features feature_get_features feature_load_fasta feature_load_featureprops feature_load_gff feature_load_go load_blast load_interpro organism_add_organism organism_delete_all_organisms organism_delete_organisms organism_get_organisms phylogeny_gene_families phylogeny_gene_order phylogeny_load_tree Galaxy tools allowing to load data into a remote Chado database.Chado is a member of the GMOD family of tools.https://github.com/galaxy-genome-annotation/python-chado 0
python-chado
To update
askomics_integrate Galaxy tools allowing to interact with a remote AskOmics server.AskOmics is a visual SPARQL query builder for RDF database.https://github.com/askomics/ 0
askocli
To update
create_account feat_from_gff3 create_or_update delete_features delete_organism export fetch_jbrowse iframe list_organism Access an Apollo instance from Galaxy 4826
apollo
To update
UseGalaxy.cz9 UseGalaxy.eu9 UseGalaxy.no9
0.0.2 msp_split [Metabolomics][LC-MS][DIMS][MS/MS] msPurity - R package for precursor ion purity assessments, data processing and spectral matching for LC-MS(/MS) and DI-MS(/MS) data 0
To update
1.28.0 mspurity_averagefragspectra mspurity_combineannotations mspurity_createdatabase mspurity_createmsp mspurity_dimspredictpuritysingle mspurity_filterfragspectra mspurity_flagremove mspurity_frag4feature mspurity_puritya mspurity_purityx mspurity_spectralmatching [Metabolomics][LC-MS][DIMS][MS/MS] msPurity - R package for precursor ion purity assessments, data processing and spectral matching for LC-MS(/MS) and DI-MS(/MS) data 11640
bioconductor-mspurity
To update
UseGalaxy.cz10 UseGalaxy.eu10 UseGalaxy.fr11 UseGalaxy.no10
2.4.5+galaxy3 metfrag [Metabolomics][LC-MS][MS/MS] MetFrag - Perform metfrag analysis (can work with the output from msPurity) 590
metfrag
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1
2.4.5+galaxy0 metfrag_vis [Metabolomics][LC-MS][MS/MS] This tool summarises the results generated by MetFrag 52
metfrag
To update
UseGalaxy.cz1 UseGalaxy.eu1
33 cfmid Competitive Fragmentation Modeling (CFM) 0
cfm
Up-to-date
4.4.0 abims_xcms_fillPeaks abims_xcms_group abims_xcms_refine abims_xcms_retcor abims_xcms_summary abims_xcms_xcmsSet msnbase_readmsdata xcms_export_samplemetadata xcms_merge xcms_plot_chromatogram xcms_plot_eic xcms_plot_raw Biological imaging Data visualisation Metabolomics Mass spectrum visualisation Label-free quantification Validation Chromatographic alignment Peak detection Chromatogram visualisation Data filtering 2728715
bioconductor-xcms
Up-to-date
UseGalaxy.be6 UseGalaxy.cz10 UseGalaxy.eu12 UseGalaxy.fr12 UseGalaxy.no9 UseGalaxy.or11
1.0.0+galaxy1 W4Mconcatenate [W4M][Utils] concatenate two Metadata tables 4
r-base
To update
UseGalaxy.fr1
1.0.0 skyline2isocor Converting skyline output to IsoCor input 115
skyline2isocor
Up-to-date
UseGalaxy.eu1 UseGalaxy.fr1
1.0.1 physiofit_data_manager Handling of physiofit input files 9
physiofit_data_manager
Up-to-date
UseGalaxy.fr1
3.4.0 physiofit PhysioFit is a scientific tool designed to quantify cell growth parameters and uptake & production fluxes 28
physiofit
Up-to-date
UseGalaxy.fr1
1.0.7+galaxy2 normalization [Metabolomics][W4M][ALL] Normalization (operation applied on each individual spectrum) of preprocessed data 3444
r-batch
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
NMR_Preprocessing NMR_Read [Metabolomics][W4M][NMR] NMR Preprocessing - Preprocessing of 1D NMR spectra from FID to baseline correction 2746
r-ggplot2
To update
UseGalaxy.cz2 UseGalaxy.eu2 UseGalaxy.fr2 UseGalaxy.no2 UseGalaxy.or2
2.0.0+galaxy3 2DNmrAnnotation [Metabolomics][W4M][NMR] NMR Annotation2D - Automatic annotation of bi-dimensional NMR spectra 57
r-batch
To update
UseGalaxy.fr1
3.0.0+galaxy1 NmrAnnotation [Metabolomics][W4M][NMR] NMR Annotation - Annotation of complex mixture NMR spectra and metabolite proportion estimation 423
libgfortran
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1
1.0.0+galaxy1 mzxmlshaper Convert mzML, mzXML or netCDF files to mzML or mzXML 502
r-base
To update
UseGalaxy.fr1
2.2.1 ms2snoop [W4M][Utils] Extraction et nettoyage des spectre MS1/2 post-traitement MSPurity. 157
r-base
To update
UseGalaxy.fr1
3.1.0+galaxy1 mixmodel4repeated_measures [Metabolomics][W4M][Statistics] Mixed models - Analysis of variance for repeated measures using mixed model 305
r-lme4
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1
1.0.0 kmd_hmdb_data_plot retrieves data from KMD HMDB API and produce plot and csv file 0
click
To update
1.3.1 isoplot Isoplot is a software for the visualisation of MS data from C13 labelling experiments 137
jinja2
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1
ipo
1.10.0 ipo4retgroup ipo4xcmsSet [W4M][LC-MS] IPO 0
bioconductor-ipo
To update
2.0.1 intens_check Statistical measures, number of missing values and mean fold change for metabolomics data. 7866
r-base
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
7.0.1 influx_si metabolic flux estimation based on [in]stationary labeling 18
influx_si
To update
UseGalaxy.fr1
1.0.2 influx_data_manager Handling influx_si data inputs in Galaxy workflows 9
influx-si-data-manager
To update
UseGalaxy.fr1
genform genform: generation of molecular formulas by high-resolution MS and MS/MS data 68
genform
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.2.1 gcms2isocor Corrective method dedicated to Isocor for calculating carbon isotopologue distribution from GCMS runs 0
To update
1.0.1+galaxy2 correlation_analysis [Metabolomics][W4M] Metabolites Correlation Analysis 231
r-batch
To update
UseGalaxy.fr1
1.48.0 abims_CAMERA_annotateDiffreport abims_CAMERA_combinexsAnnos CAMERA_findAdducts CAMERA_findIsotopes CAMERA_groupCorr CAMERA_groupFWHM 16515
r-snow
To update
UseGalaxy.be1 UseGalaxy.cz2 UseGalaxy.eu2 UseGalaxy.fr6 UseGalaxy.no2 UseGalaxy.or2
0.2.5+galaxy1 wade identify regions of interest 0
wade
To update
1.1.0 tree_relabel Relabels the tips of a newick formatted tree. 0
perl-bioperl
To update
1.1.0 stringmlst Rapid and accurate identification of the sequence type (ST) 0
stringMLST
To update
0.11.0 staramr_search Scan genome contigs against the ResFinder, PlasmidFinder, and PointFinder antimicrobial resistance databases. Microbiology Public health and epidemiology Infectious disease Antimicrobial resistance prediction 51323
staramr
Up-to-date
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
0.3.7 srst2 Short Read Sequence Typing for Bacterial Pathogens 387
srst2
To update
UseGalaxy.cz1 UseGalaxy.eu1
1.0.1 spolpred A program for predicting the spoligotype from raw sequence reads 0
spolpred
To update
0.3.3 spatyper Determines SPA type based on repeats in a submitted staphylococcal protein A fasta file. 0
spatyper
Up-to-date
1.1.2+galaxy1 spades_header_fixer Fixes Spades Fasta ids 0
sed
To update
0.7.6 smalt SMALT aligns DNA sequencing reads with a reference genome. 0
smalt
Up-to-date
1.1.3 sistr_cmd SISTR in silico serotyping tool Whole genome sequencing Immunoproteins and antigens Sequence assembly Zoology Public health and epidemiology Genome assembly Visualisation Multilocus sequence typing 4863
sistr_cmd
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
1.0.1 seqtk_nml_sample Tool to downsample fastq reads 0
seqtk
To update
0.1.2 refseq_masher_contains refseq_masher_matches Find what genomes match or are contained within your sequence data using Mash_ and a Mash sketch database. 5661
refseq_masher
Up-to-date
UseGalaxy.eu2 UseGalaxy.fr2 UseGalaxy.or2
0.7.0 aacoverage aavariants callcodonvar callntvar complexity_bam complexity_fasta consensus distance dnds drmutations hydra quality A collection of tools for analysing Viral Quasispecies 14279
quasitools
Up-to-date
UseGalaxy.fr12 UseGalaxy.or12
1.0.0 pseudogenome Create a pseudogenome from a multiple fasta file either with a JCVI linker or custom length and characters. 0
perl-bioperl
To update
1.2 promer4_substitutions Aligns two sets of contigs and reports amino acid substitutions between them 0
python
To update
1.2.1 pneumocat Pneumococcal Capsular Typing of illumina fastq reads 0
pneumocat
Up-to-date
1.1 plasmidspades Genome assembler for assemblying plasmid 0
spades
To update
Plasmid Profiler suite defining all dependencies for Plasmid Profiler 0
To update
0.1.6 plasmid_profiler Explores plasmid content in WGS data 0
r
To update
0.1.2 patrist Extract Patristic Distance From a Tree 0
python
To update
1.1.14 pangolin Phylogenetic Assignment of Named Global Outbreak LINeages 19682
pangolin
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
0.1.4.1 mykrobe_parseR RScript to parse the results of mykrobe predictor. 0
r-base
To update
1.0.2 mrbayes A program for the Bayesian estimation of phylogeny. 0
mrbayes
To update
UseGalaxy.be1 UseGalaxy.eu1
3.1.9 mob_recon mob_typer MOB-suite is a set of software tools for clustering, reconstruction and typing of plasmids from draft assemblies Metagenomics Sequence assembly Genotype and phenotype Mobile genetic elements Genomics Clustering Sequence analysis 193569
mob_suite
Up-to-date
UseGalaxy.cz2 UseGalaxy.eu2 UseGalaxy.fr2 UseGalaxy.or2
1.0.10 mauve_contig_mover Order a draft genome relative to a related reference genome 0
mauve
To update
2.3 kat_@EXECUTABLE@ SEquence Coverage estimator Tool. Estimates the coverage of each sequence in a file using K-mers from another sequence file. 0
kat
To update
2.3 kat_@EXECUTABLE@ Filtering kmers or reads from a database of kmers hashes 0
kat
To update
0.3.0 kaptive Kaptive reports information about capsular (K) loci found in genome assemblies. 0
kaptive
To update
1.0.1 hivtrace An application that identifies potential transmission clusters within a supplied FASTA file with an option to find potential links against the Los Alamos HIV Sequence Database. 0
hivtrace
To update
1.1.0 gnali A tool to find nonessential, loss-of-function gene variants 0
gnali
Up-to-date
0.1.4.1 getmlst Download MLST datasets by species from pubmlst.org 0
srst2
To update
1.0.1 filter_spades_repeat Remove short and repeat contigs/scaffolds 0
perl-bioperl
To update
0.1.0 feht Automatically identify makers predictive of groups. 0
feht
To update
1.2 FastQC_Summary Summary multiple FastQC into a single tabular line report 0
perl-bioperl
To update
1.1.0 fa-extract-sequence extract single fasta from multiple fasta file 1837
perl-bioperl
To update
1.0.0 fasta2bed Convert multiple fasta file into tabular bed file format 0
perl-bioperl
To update
2.0.0 ectyper EC-Typer - in silico serotyping of Escherichia coli species Whole genome sequencing Public health and epidemiology Sequence assembly Genotype and phenotype Workflows Sequence assembly Read pre-processing Variant calling 16579
ectyper
Up-to-date
UseGalaxy.cz1 UseGalaxy.eu1
0.20.0 csvtk_awklike_filter csvtk_awklike_mutate csvtk_collapse csvtk_concat csvtk_convert csvtk_correlation csvtk_cut csvtk_filter csvtk_freq csvtk_gather csvtk_join csvtk_mutate csvtk_plot csvtk_replace csvtk_sample csvtk_separate csvtk_sort csvtk_split csvtk_summary csvtk_uniq Rapid data investigation and manipulation of csv/tsv files 124
csvtk
To update
UseGalaxy.fr1 UseGalaxy.or6
1.0 CryptoGenotyper CryptoGenotyper is a standalone tool to *in-silico* determine species and subtype based on SSU rRNA and gp60 markers. 11902
cryptogenotyper
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.2 concat_fastqs Concatenate paired datasets 0
To update
0.1 combine Combine Tabular Collection into a single file 0
To update
1.0 combine_stats Combine multiple Assemblystats datasets into a single tabular report 0
perl-getopt-long
To update
0.1 combine_json JSON collection tool that takes multiple JSON data arrays and combines them into a single JSON array. 0
To update
5.1.0 collapse_dataset Collection tool that collapses a list of files into a single datasset in order of appears in collection 99100
gawk
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1 UseGalaxy.or1
1.3.0 bundle_collection Tool to bundle up list collection into a single zip to be download 3600
perl-getopt-long
To update
UseGalaxy.fr1 UseGalaxy.or1
0.2.0 bionumeric_convert Convert BioHansel output data to a Bionumerics friendly form 0
pandas
To update
2.4.0 biohansel Heidelberg and Enteritidis SNP Elucidation 0
bio_hansel
To update
1.0.0 bamclipper Soft-clip gene-specific primers from BAM alignment file based on genomic coordinates of primer pairs in BEDPE format. 0
bamclipper
Up-to-date
1.1.0 bam2mappingstats Generates mapping stats from a bam file. 0
perl
To update
1.1.0 assemblystats Summarise an assembly (e.g. N50 metrics) 0
perl-bioperl
To update
1.1 abacas Order and Orientate Contigs 0
mummer
To update
UseGalaxy.fr1
13.45.0.4846264 t_coffee T-Coffee 9236
t-coffee
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.0 smina Scoring and Minimization with smina 549
smina
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
0.1.0 smart_domains SMART domains 0
perl-bioperl
To update
0.1 replace_chromosome_names Replace chromosome names 579
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.0 rdock Docking ligands to proteins and nucleic acids 0
rDock
To update
1.0 plotheatmap Plot heatmap of gene expression data 0
bioconductor-preprocesscore
To update
3.3a+galaxy1 miranda Finds potential target sites for miRNAs in genomic sequences 7099
miranda
To update
UseGalaxy.eu1 UseGalaxy.fr1
2.32 lotus2 LotuS2 OTU processing pipeline Metagenomics Taxonomy Microbial ecology Sequence feature detection DNA barcoding 1747
lotus2
To update
UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.or1
0.3.0 hcluster_sg_parser Converts hcluster_sg 3-column output into lists of ids 297
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.5.1.1 hcluster_sg Hierarchically clustering on a sparse graph 287
hcluster_sg
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.4.3 gstf_preparation GeneSeqToFamily preparation converts data for the workflow 401
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
0.91b gblocks Gblocks 580
gblocks
Up-to-date
UseGalaxy.be1 UseGalaxy.fr1 UseGalaxy.or1
0.1.0 export_to_cluster Export datasets to cluster 0
python
To update
ete
3.1.3 ete_gene_csv_finder ete_genetree_splitter ete_homology_classifier ete_init_taxdb ete_lineage_generator ete3_mod ete_species_tree_generator Analyse phylogenetic trees using the ETE Toolkit Phylogenetics Phylogenetic analysis Phylogenetic tree editing 985
ete
ete3
To update
UseGalaxy.cz7 UseGalaxy.eu7 UseGalaxy.fr7 UseGalaxy.no7
0.2.0 blast_parser Convert 12- or 24-column BLAST output into 3-column hcluster_sg input 563
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.0+galaxy1 apoc Large-scale structural comparison of protein pockets 9
apoc
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1 UseGalaxy.or1
1.9.2.post0 treebest_best TreeBeST best Phylogenetics Phylogenetic tree visualisation Phylogenetic analysis Phylogenetic inference (from molecular sequences) 1025
treebest
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.fr1 UseGalaxy.no1
0.4.1 gafa Gene Align and Family Aggregator 47
python
To update
UseGalaxy.cz1 UseGalaxy.eu1 UseGalaxy.no1
1.0.0 get_feature_info get_genetree get_sequences A suite of Galaxy tools designed to work with Ensembl REST API. 2927
python
To update
UseGalaxy.cz3 UseGalaxy.eu3 UseGalaxy.no3
2.1 peptimapper_clustqualify peptimapper_clust_to_gff peptimapper_pep_match peptimapper_pep_novo_tag Proteogenomics workflow for the expert annotation of eukaryotic genomes 6
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UseGalaxy.fr4
0.1.0 openlabcds2csv Creates a summary of several "Internal Standard Report" OpenLabCDS results. 0
openjdk
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0.2 miranda2asko Converts miRanda output into AskOmics format 0
perl
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1.5.2 meneco Meneco computes minimal completions to your draft network with reactions from a repair network 0
meneco
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1.7.8 logol_wrapper Logol is a pattern matching grammar language and a set of tools to search a pattern in a sequence 0
logol
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0.3.3 helixer Gene calling with Deep Neural Networks Sequence analysis Gene transcripts Gene prediction Genome annotation 1013
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0.3 get_pairs Separate paired and unpaired reads from two fastq files 0
python
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0.1.0 gcms2isocor Conversion from GCMS PostRun Analysis to Isocor 0
openjdk
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0.1 feelnc2asko Convert FeelNC GTF to GFF3 0
perl-bioperl
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3.0.8 braker3 BRAKER3 is a pipeline for fully automated prediction of protein coding gene structures with GeneMark-ES/ET and AUGUSTUS in novel eukaryotic genomes . RNA-Seq Genomics Structure prediction Sequence analysis Genome annotation Gene prediction 3928
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2.1.6 braker BRAKER is a pipeline for fully automated prediction of protein coding gene structures with GeneMark-ES/ET and AUGUSTUS in novel eukaryotic genomes . 217
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UseGalaxy.be1 UseGalaxy.cz1 UseGalaxy.eu1
1.1.0 baric_archive_rennes baric_archive_toulouse A data source tool to fetch data from a BARIC Archive server. 16
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UseGalaxy.fr2
0.2 askor_de AskoR links EdgeR and AskOmics 3
bioconductor-limma
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