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).

Version:	1.3.0
Depends:	R (≥ 3.6.0)
Imports:	data.table, graphics, colorspace, R.utils, qgraph, stringr
Suggests:	rmarkdown, knitr, testthat (≥ 3.0.0), covr
Published:	2024-09-20
DOI:	10.32614/CRAN.package.rCNV
Author:	Piyal Karunarathne [aut, cre], Qiujie Zhou [aut], Klaus Schliep [aut], Pascal Milesi [aut]
Maintainer:	Piyal Karunarathne <piyalkarumail at yahoo.com>
BugReports:	https://github.com/piyalkarum/rCNV/issues
License:	AGPL (≥ 3)
URL:	https://piyalkarum.github.io/rCNV/, https://cran.r-project.org/package=rCNV
NeedsCompilation:	no
Language:	en-US
Citation:	rCNV citation info
Materials:	README, NEWS
CRAN checks:	rCNV results

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