piyalkarum/rCNV: Detect Copy Number Variants from SNPs Data
Functions in this package will import filtered variant call format (VCF) files of SNPs data and generate data sets to detect copy number variants, visualize them and do downstream analyses with copy number variants(e.g. Environmental association analyses).
Getting started
Browse package contents
Package details |
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| Maintainer | Piyal Karunarathne <piyalkarumail@yahoo.com> |
| License | AGPL (>= 3) |
| Version | 1.3.900 |
| URL | https://piyalkarum.github.io/rCNV/ https://cran.r-project.org/package=rCNV |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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