Reads supporting a variant

dkoboldt / varscan

Variant calling and somatic mutation/CNV detection for next-generation sequencing data

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Open biounix opened 3 years ago

biounix commented 3 years ago

Hi,

Can VarScan report the specific read IDs that support each variant in addition to just the number of reads?

If not, is that a feature that could be implemented?

Many thanks,