groupCNVs-methods

methods

CNVrd2 uses next-generation sequencing data to measure human gene copy number for multiple samples,
indentify SNPs tagging copy number variants and detect copy
number polymorphic genomic regions.

Hoang Tan Nguyen

CNVrd2

CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.

groupCNVs-methods function

<dl> <dt><code>signature(Object = "clusteringCNVs")</code></dt><dd> </dd> </dl>

groupCNVs-methods: Method `groupCNVs`

Description

Arguments

Methods