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

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.

Package details

AuthorHoang Tan Nguyen, Tony R Merriman and Mik Black
Bioconductor views Clustering. CopyNumberVariation Coverage LinkageDisequilibrium SNP Sequencing Software
MaintainerHoang Tan Nguyen <>
Package repositoryView on Bioconductor
Installation Install the latest version of this package by entering the following in R:
if (!requireNamespace("BiocManager", quietly = TRUE))


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CNVrd2 documentation built on Nov. 8, 2020, 5:30 p.m.