Hello everyone,
I'm trying to understand how GSEA works and what I have understood so far is that in GSEA we use all the genes in our RNA-seq data set and then rank them with the most expressed at the top and underexpressed at the bottom and then find the genes for particular function lying in upregulated or downregulated group. it is different than GO and KEGG where we only use DEGs that are enriched for GO terms and KEGG pathways. I came across this statement in one of the analyses where they used GO and KEGG datasets for GSEA, generating two GSEA results folders, each for GO and KEGG. this confuses me since I haven't heard in any of the tutorial people mentioning if we use the GO and KEGG datasets too for GSEA, I thought we use all the genes in our dataset. can someone please help me understand the concept?
Thank you
Thank you so much!! this clears my confusion