Thank you. I read the manual again and now makes more sense to me.
Also, what is the input file for ANNOVAR in VirusClip?
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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
From the VirusClip paper (figure1) they say that they align the reads to the virus genome, not to the host transcriptome. Therefore, no splice-aware aligner is required.
Thank you. I read the manual again and now makes more sense to me.
Also, what is the input file for ANNOVAR in VirusClip?
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