Entering edit mode
7.3 years ago
poojasethiya
▴
120
I have two RNASeq libraries ( (i.e. NEB and ScriptSeq) of same sample. I have used same pipeline to align the reads and perform further down stream analysis. But upon comparison of DEG, I get different results. About 60% of the genes UP-regulated in NEB overlap with DOWN genes in NEB. What can be the probable reason?
Thank you in advance.
