CNVrd2
CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
Bioconductor version: 3.23 · Package version: 1.50.0
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.
Installation
if (!require("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("CNVrd2")Details
| Maintainer | Hoang Tan Nguyen <hoangtannguyenvn@gmail.com> |
| Author | Hoang Tan Nguyen, Tony R Merriman and Mik Black |
| License | GPL-2 |
| URL | https://github.com/hoangtn/CNVrd2 |
| Downloads rank | 613 |
| Source branch | RELEASE_3_23 |
| biocViews | Clustering., CopyNumberVariation, Coverage, LinkageDisequilibrium, SNP, Sequencing, Software |
Download
Follow the installation instructions to use this package in your R session.
| Source package | CNVrd2_1.50.0.tar.gz |
| Windows binary (x86_64) | CNVrd2_1.50.0.zip |
| macOS binary (arm64) | CNVrd2_1.50.0.tgz |
| macOS binary (x86_64) | CNVrd2_1.50.0.tgz |