Entering edit mode
6.6 years ago
KVC_bioinfo
▴
590
Hello,
I am looking into viral integration in RNA-seq data (human samples). I came across two pipelines VirusFinder and VirusClip both of them claim that they can deal with RNA-seq data however both of them do not use a spliced aware aligner for the alignment.
I am very confused how does that work? Can someone help me with this regard?
Thank you
Thank you. I read the manual again and now makes more sense to me.
Also, what is the input file for ANNOVAR in VirusClip?