Hello, when I intercept a part of "rnk" (e.g. 30 or 50 genes) for GSEA analysis, I get an error of "No gene sets passed through filtering condition", which seems to be related to the fold-change and p-value threshold settings in "deseq", or related to other parameter settings, but I tried to modify it, and failed to solve the problem, Do you have any suggestions?
Hello, when I intercept a part of "rnk" (e.g. 30 or 50 genes) for GSEA analysis, I get an error of "No gene sets passed through filtering condition", which seems to be related to the fold-change and p-value threshold settings in "deseq", or related to other parameter settings, but I tried to modify it, and failed to solve the problem, Do you have any suggestions?