bioconductor.org : CNVrd2
CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
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Source
- Documentation
- JSON
purl: pkg:bioconductor/CNVrd2
Keywords:
Clustering.
, CopyNumberVariation
, Coverage
, LinkageDisequilibrium
, SNP
, Sequencing
, Software
License: GPL-2.0
Latest release: 3 months ago
First release: almost 2 years ago
Downloads: 27,284 total
Stars: 3 on GitHub
Forks: 3 on GitHub
See more repository details: repos.ecosyste.ms
Last synced: 1 day ago