Hi All. I am new to bioinformatics, and am trying to run subReads featureCounts to analyze RNA seq data. I am using the code below, and am in the featureCounts...
DESeq factor design, and optimal number of samples
For the 1st question, I want to know if I should run a single factor or double factor. These samples are match normal/tumor from different patients so...
Hello all. I have a set of DE genes from a single replicate as identified by the GFOLD package. Though I am getting results which have the same gene ID...