• Home
  • Course structure
  • Linux containers
  • Introduction
  • mRNA-seq
  • Analysis workflow
  • Data repositories
  • Course data
  • Experimental design
  • Read QC and trimming
  • Read mapping and reference genome
  • STAR mapping, BAM/SAM/CRAM and QualiMap
  • Genome Browser
  • Salmon mapping
  • MultiQC report
  • R basics
  • Differential expression analysis
  • Functional analysis
  • Small project in groups
  • Resources

    DESeq2

    • Vignette
    • Tutorial

    On filtering low counts and DE analysis of low-expressed genes

    • Heavy-tailed prior distributions for sequence count data: removing the noise and preserving large differences. Bioinformatics, 2019.
    • Inferential considerations for low-count RNA-seq transcripts: a case study on the dominant prairie grass Andropogon gerardii. BMC Genomics, 2016.
    • consensusDE: an R package for assessing consensus of multiple RNA-seq algorithms with RUV correction. PeerJ. 2019.

    Adjusted p-value and multiple testing

    • Why, When and How to Adjust Your P Values? Cell J, 2019.
    • How does multiple testing correction work? Nat Biotechnol, 2009.

    Online course materials

    • https://github.com/hbctraining/rnaseq_overview
    • http://chagall.med.cornell.edu/RNASEQcourse/
    • https://galaxyproject.org/tutorials/rb_rnaseq/

    References

    • A survey of best practices for RNA-seq data analysis. Conesa et al., Genome Biology, 2016.
    • Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet. 2009 Jan;10(1):57-63. doi: 10.1038/nrg2484.