Genotyping Variant Calls

vplagnol / ExomeDepth

ExomeDepth R package for the detection of copy number variants in exomes and gene panels using high throughput DNA sequencing data.

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Open justin-greenblatt opened 8 months ago

justin-greenblatt commented 8 months ago

Is there any function for genotyping CNV calls? Defining if it is a Heterozygous or Homozygous variant? Thanks Best Regards :)