emnormalCNV-methods


  Implement the Expectation Maximization


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.

emnormalCNV-methods function

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

emnormalCNV-methods: Method `emnormalCNV`

Description

Arguments

Methods