Hi,
I'm performing Gene Ontology (GO) enrichment analysis on differentially expressed genes (DEGs) from ATAC-seq data, using R (clusterProfiler). After separating my DEGs (DEseq2) into up-regulated and down-regulated gene sets based on log2 fold change and adjusted p-value thresholds, I noticed that the GO pathway analysis for both sets returns similar or identical enriched pathways.
Has anyone encountered this issue? What could be causing the same GO terms to appear in both up- and down-regulated gene sets? As output from DEseq2, the genes from the two list cannot be shared.
ATAC-seq measures chromatin openness, not expression, so you shouldn't call these genes differential expressed genes. They are differentially accessible genes. Further, it is likely that any change in openness is not uniformally distributed across the genes. At least in my experience, genes that are upregulated at the expression level to not neccessarily increase in openness at the chromatin level and vice-versa.