Hi I have run differential expression analysis in cancer RNA-seq data vs Normal the data was from TCGA I manage to get result file.
I set the logfold change 2 and alpha 0.001
what I expect to see less number of genes down and up regulated my question what is the best way to downstream or selecting final result ??
Thanks in advance Nasr
If you post over at biostars.org (which you are welcome to do) please be sure to add more details and all relevant command lines. Currently it is difficult to advise you since from what you write it is unclear what you are actually doing.