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).
- Version1.3.0
- R versionunknown
- LicenseAGPL (≥ 3)
- Needs compilation?No
- Languageen-US
- rCNV citation info
- Last release09/20/2024
Documentation
Team
Piyal Karunarathne
Klaus Schliep
Pascal Milesi
Qiujie Zhou
Insights
Last 30 days
Last 365 days
The following line graph shows the downloads per day. You can hover over the graph to see the exact number of downloads per day.
Data provided by CRAN
Binaries
Dependencies
- Imports5 packages
- Suggests4 packages