Thanks, but I wanted to do the DE analysis myself in R. I'm not able to customize Trinity's parameters to my liking but wasn't sure if I could upload my RSEM values into R.
I have a series of de novo assembled reads from Trinity from an organism without an annotated genome. I was wondering if it was possible to use DESeq2 through R to do my diffrerential expression analysis. I quantified my gene/transcript counts using RSEM.
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Wonder no more! Read the manual and dispel any doubts you may have:
Differential Expression Analysis Using a Trinity Assembly
Spoiler:
Trinity provides support for several differential expression analysis tools, currently including the following R packages:
edgeR : http://bioconductor.org/packages/release/bioc/html/edgeR.html
DESeq2: http://bioconductor.org/packages/release/bioc/html/DESeq2.html
limma/voom: http://bioconductor.org/packages/release/bioc/html/limma.html
ROTS: http://www.btk.fi/research/research-groups/elo/software/rots/
When you run Trinity wrapper scripts, it creates R scripts to run the differential expression analysis. You can then edit the scripts to your liking and run them.
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Why not? DESeq2 can work with count table of everything.