Transcriptomics
Training material for all kinds of transcriptomics analysis.
Requirements
Before diving into this topic, we recommend you to have a look at:
- Introduction to Galaxy Analyses
- slides Slides: Quality Control
- tutorial Hands-on: Quality Control
- slides Slides: Mapping
- tutorial Hands-on: Mapping
Material
You can view the tutorial materials in different languages by clicking the dropdown icon next to the slides (slides) and tutorial (tutorial) buttons below.Introduction
Start here if you are new to RNA-Seq analysis in Galaxy
Lesson | Slides | Hands-on | Recordings | Input dataset | Workflows |
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Introduction to Transcriptomics
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Reference-based RNA-Seq data analysis | |||||
De novo transcriptome reconstruction with RNA-Seq
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End-to-End Analysis
These tutorials take you from raw sequencing reads to pathway analysis
Lesson | Slides | Hands-on | Recordings | Input dataset | Workflows |
---|---|---|---|---|---|
1: RNA-Seq reads to counts | |||||
2: RNA-seq counts to genes | |||||
3: RNA-seq genes to pathways |
Visualisation
Tutorials covering data visualisation
Other
Assorted Tutorials
Galaxy instances
You can use a public Galaxy instance which has been tested for the availability of the used tools. They are listed along with the tutorials above.
You can also use the following Docker image for these tutorials:
docker run -p 8080:80 quay.io/galaxy/transcriptomics-training
NOTE: Use the -d flag at the end of the command if you want to automatically download all the data-libraries into the container.
It will launch a flavored Galaxy instance available on http://localhost:8080. This instance will contain all the tools and workflows to follow the tutorials in this topic. Login as admin with password password to access everything.
Frequently Asked Questions
Common questions regarding this topic have been collected on a dedicated FAQ page . Common questions related to specific tutorials can be accessed from the tutorials themselves.
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Editorial Board
This material is reviewed by our Editorial Board:
Bérénice Batut Maria Doyle Florian HeylContributors
This material was contributed to by:
Anthony Bretaudeau José Manuel Domínguez IGC Bioinformatics Unit Markus Wolfien Björn Grüning Mateo Boudet Sofoklis Keisaris Daniel Maticzka Charity Law Lucille Delisle Jovana Maksimovic Matt Ritchie Helena Rasche Toby Hodges Clemens Blank Mira Kuntz Olivier Dameron Beatriz Serrano-Solano Marek Ostaszewski Saskia Hiltemann Peter van Heusden Xavier Garnier The Carpentries Belinda Phipson Xi Liu James Taylor Iacopo Cristoferi Sanjay Kumar Srikakulam Andrea Bagnacani Clea Siguret Erwan Corre Shian Su Nicola Soranzo Bérénice Batut Cristóbal Gallardo Matti Hoch Anna Trigos Mallory Freeberg Anton Nekrutenko Florian Heyl Chao Zhang Fotis E. Psomopoulos Mo Heydarian Maria Doyle Pavankumar Videm Harriet Dashnow Myrthe van Baardwijk Anika Erxleben Anne Siegel Gildas Le CorguilléFunding
These individuals or organisations provided funding support for the development of this resource
References
- Shirley Pepke et al: Computation for ChIP-seq and RNA-seq studies
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Paul L. Auer & R. W. Doerge: Statistical Design and Analysis of RNA Sequencing Data
Insights into proper planning of your RNA-seq run! To read before any RNA-seq experiment! -
Ian Korf: Genomics: the state of the art in RNA-seq analysis
A refreshingly honest view on the non-trivial aspects of RNA-seq analysis -
Marie-Agnès Dillies et al: A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysis
Systematic comparison of seven representative normalization methods for the differential analysis of RNA-seq data (Total Count, Upper Quartile, Median (Med), DESeq, edgeR, Quantile and Reads Per Kilobase per Million mapped reads (RPKM) normalization) -
Franck Rapaport et al: Comprehensive evaluation of differential gene expression analysis methods for RNA-seq data
Evaluation of methods for differential gene expression analysis - Charlotte Soneson & Mauro Delorenzi: A comparison of methods for differential expression analysis of RNA-seq data
- Adam Roberts et al: Improving RNA-Seq expression estimates by correcting for fragment bias
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Manuel Garber et al: Computational methods for transcriptome annotation and quantification using RNA-seq
Classical paper about the computational aspects of RNA-seq data analysis - Cole Trapnell et al: Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
- Zhong Wang et al: RNA-Seq: a revolutionary tool for transcriptomics
- Dittrich, M. T. and Klau, G. W. and Rosenwald, A. and Dandekar, T. and Muller, T.: Identifying functional modules in protein-protein interaction networks: an integrated exact approach
- May, Ali; Brandt, Bernd W; El-Kebir, Mohammed; Klau, Gunnar W; Zaura, Egija; Crielaard, Wim; Heringa, Jaap; Abeln, Sanne: metaModules identifies key functional subnetworks in microbiome-related disease
- Pavankumar, Videm; Dominic, Rose; Fabrizio, Costa; Rolf, Backofen: BlockClust: efficient clustering and classification of non-coding RNAs from short read RNA-seq profiles