Hello, I have RNA-seq data with log2 fold changes in gene expression along with adjusted p values. If I transform the fold changes to linear fold changes, how do I transform the adjusted p values?
Secondly, where can I find the error between biological replicates that was found in the RNA-seq experiment? I did not analyze the raw data myself; I had a vendor send me the DGE data. I can see DGE levels for individual samples/replicates, but I can't find already calculated error statistics between replicates.