Hi,
I'm putting together a database to compare gene expression across many different RNA-seq experiments. I have multiple DESeq2 normalized counts matrices from the different experiments.
My question is am I able to merge these normalized counts matrices by gene names and directly compare the gene expression across all of these experiments? Or will I have to re-run DESeq2 with all samples together to have the normalization done together?
Thanks, Matt
The DeSeq2 normalizes counts with respect to library size. So in principal it should be able to compare different sequencing runs together even with different library sizes.