Hi
I want to find virus integration sites in a genome we sequenced. Is it more reasonable to blast the resulted contigs or maybe blast the reads themselves would be more productive?
Do you have any other idea how to "catch" those integration sites?
Thank you!
I want to find virus integration sites in a genome we sequenced. Is it more reasonable to blast the resulted contigs or maybe blast the reads themselves would be more productive?
Do you have any other idea how to "catch" those integration sites?
Thank you!
Comment