Shrinking fold change and dispersion for RNA-seq data ( DESeq2)
Hello biostars,
I'm new to RNA-seq and I'm trying to introduce myself to DESeq2.
My question is: Why do we need to shrink the fold change and dispersion for RNA-seq data?
Thanks in advance
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1 answer
I'd recommend trying to read the DESeq2 paper from 2014 (we wrote it with non-statisticians in mind), but you might also try this post on another thread:
A: Can someone please explain in simple terms how DESeq2 works?
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