XHMM on whole genome sequencing data

Hello,

Has anyone used XHMM for CNV detection in whole-genome sequencing data? I am planning to do this using a dummy capture kit containing all human exons. Is this reasonable?

Thans

xhmm wgs whole-genome sequencing cnv

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written 10.5 years ago by wanabi •

XHMM is supposed to be used in exome data, because the calls are based on the average coverage of each exon.

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updated 7.9 years ago by Ram

• written 10.5 years ago by Leandro Lima

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