Bug Bulletin: The GenomeLocPArser error in SplitNCigarReads has been fixed; if you encounter it, use the latest nightly build.

how do you usually select variants on VCF files?

rcholicrcholic DenverPosts: 67Member

I would like to know what's the common standards for filtering VCF files? do you filter by depth of coverage or anything else? for exome-sequencing

Answers

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