Workflows
These workflows are associated with Identifying tuberculosis transmission links: from SNPs to transmission clusters
To use these workflows in Galaxy you can either click the links to download the workflows, or you can right-click and copy the link to the workflow which can be used in the Galaxy form to import workflows.
From BAMs to drug resistance prediction with TB-profiler
Last updated Mar 16, 2022
Launch in Tutorial Mode
License:
None Specified, defaults to
CC-BY-4.0
Tests: ❌
Results: Not yet automated
flowchart TD 0["ℹ️ Input Collection\nMTB single-end BAMs"]; style 0 stroke:#2c3143,stroke-width:4px; 1["ℹ️ Input Collection\nMTB paired-end BAMs"]; style 1 stroke:#2c3143,stroke-width:4px; 2["Merge collections"]; 0 -->|output| 2; 1 -->|output| 2; 3["Samtools view BAM > SAM"]; 2 -->|output| 3; aa220027-9d10-4328-b2c2-e4d139d5d5bd["Output\nSamtools view on input dataset(s): filtered alignments"]; 3 --> aa220027-9d10-4328-b2c2-e4d139d5d5bd; style aa220027-9d10-4328-b2c2-e4d139d5d5bd stroke:#2c3143,stroke-width:4px; 4["Sed MTB_anc to Chromosome"]; 3 -->|outputsam| 4; 5["Samtools view SAM > BAM"]; 4 -->|output| 5; 6["TB-profiler"]; 5 -->|outputsam| 6; 7["Get drug resistance profile"]; 6 -->|output_txt| 7; 8["Add Sample Name"]; 7 -->|output| 8; 9["Concatenate DR profiles in a single table"]; 8 -->|output| 9; 10["Cleanup the table"]; 9 -->|out_file1| 10;
From Fastqs to VCFs and BAMs
Last updated Mar 16, 2022
Launch in Tutorial Mode
License:
None Specified, defaults to
CC-BY-4.0
Tests: ❌
Results: Not yet automated
flowchart TD 0["ℹ️ Input Collection\nSingle-End FASTQs"]; style 0 stroke:#2c3143,stroke-width:4px; 1["ℹ️ Input Collection\nPaired-End FASTQs"]; style 1 stroke:#2c3143,stroke-width:4px; 2["ℹ️ Input Dataset\nMycobacterium_tuberculosis_ancestral_reference.gbk"]; style 2 stroke:#2c3143,stroke-width:4px; 3["Trimmomatic"]; 0 -->|output| 3; 4["Trimmomatic"]; 1 -->|output| 4; 5["Mapping and variant calling of SINGLE END FASTQs with snippy"]; 3 -->|fastq_out| 5; 2 -->|output| 5; 6["Mapping and variant calling of PAIRED END FASTQs with snippy"]; 4 -->|fastq_out_paired| 6; 2 -->|output| 6; 7["Merge PE/SE VCFs in a single collection with all samples"]; 5 -->|snpvcf| 7; 6 -->|snpvcf| 7; 8["Merge PE/SE BAMs in a single collection with all samples Part the workflow ”Identifying DR with TB-profiler"]; 5 -->|snpsbam| 8; 6 -->|snpsbam| 8; 9["TB Variant Filter"]; 7 -->|output| 9;
From VCFs to SNP distance matrix
Last updated Mar 16, 2022
Launch in Tutorial Mode
License:
None Specified, defaults to
CC-BY-4.0
Tests: ❌
Results: Not yet automated
flowchart TD 0["ℹ️ Input Collection\nCollection of VCFs to analyze"]; style 0 stroke:#2c3143,stroke-width:4px; 1["ℹ️ Input Dataset\nReference genome of the MTBC ancestor"]; style 1 stroke:#2c3143,stroke-width:4px; 2["Filter TB variants"]; 0 -->|output| 2; 3["Generate the complete genome of each of the samples"]; 2 -->|output1| 3; 1 -->|output| 3; ce5dd7a2-c33d-46b4-9f02-68c2bdfcf31a["Output\n#{input_file}"]; 3 --> ce5dd7a2-c33d-46b4-9f02-68c2bdfcf31a; style ce5dd7a2-c33d-46b4-9f02-68c2bdfcf31a stroke:#2c3143,stroke-width:4px; 4["Concatenate genomes to build a MSA"]; 3 -->|output_file| 4; 5["Keep only variable positions"]; 4 -->|out_file1| 5; 6["Calculate SNP distances"]; 5 -->|output_fasta| 6;
Importing into Galaxy
Below are the instructions for importing these workflows directly into your Galaxy server of choice to start using them!Hands-on: Importing a workflow
- Click on Workflow on the top menu bar of Galaxy. You will see a list of all your workflows.
- Click on galaxy-upload Import at the top-right of the screen
- Provide your workflow
- Option 1: Paste the URL of the workflow into the box labelled “Archived Workflow URL”
- Option 2: Upload the workflow file in the box labelled “Archived Workflow File”
- Click the Import workflow button
Below is a short video demonstrating how to import a workflow from GitHub using this procedure: