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).
- https://piyalkarum.github.io/rCNV/
- https://cran.r-project.org/package=rCNV
- File a bug report
- rCNV results
- rCNV.pdf
- Version1.3.0
- R version≥ 3.6.0
- LicenseAGPL (≥ 3)
- Needs compilation?No
- Languageen-US
- rCNV citation info
- Last release09/20/2024
Documentation
Team
Piyal Karunarathne
Qiujie Zhou
Klaus Schliep
Pascal Milesi
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Dependencies
- Depends1 package
- Imports6 packages
- Suggests4 packages