Thanks, Kevin
under the first situation you mention above (FPKM situation), I can determine gene A is expressed or not in a particular sample (if FPKM >=10 gene A is expressed and <10 gene A is not expressed). then I determine gene A is expressed or not in every sample (I have over 1000 sample in TCGA breast cancer samples. so I have over 1000 FPKM value for gene A) and set the second cutoff value as 25% (gene A is prevalently expressed in TCGA breast cancer sample if percentage of expressed samples for gene A is over 25%). then I have two gene sets. I do calculation above for every gene and compare percentage of prevalently expressed gene between these two sets. I want to give the conclusion that set A has more prevalently expressed gene than set B.
Is it reasonable to do so to get that conlusion?