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CNVrd2

Bioc current

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

v1.50.0 · software · GPL-2
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Release Lineage

Entered 2.13 · Oct 15, 2013

Current · Requires R 4.6

1.0 In 26 of 49 releases 3.23

Description

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.

Code & tests

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Code

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Topics

Software › AssayDomain › CopyNumberVariation
Software › AssayDomain › SNP
Software › Technology › Sequencing
Software
Software › BiologicalQuestion › Coverage
Software › BiologicalQuestion › LinkageDisequilibrium
Clustering.

People

Hoang Tan Nguyen