I apologize for asking this naive question but I have read several tutorials and I feel unsure about the following: When using gene set enrichment analyses ( ReactomePA, clusterProfiler, gprofiler2 etc.) The input data is an order ranked geneList
Is this geneList the output from DESeq2 or a filtered list for example filtered by FDC or log2FoldChange?
This is how most tutorials filter the gene set in R:
gene <- names(geneList)[abs(geneList) > 2]
Is this assigning the gene variable names of genes with values greater than the absolute value of 2?
Thanks!
I see, edited my comment, thanks.