rCNV
1.3.0Detect Copy Number Variants from SNPs Data
Overview
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).
Install
Health
- OK2026-06-0913 OK · 0 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE
- ERROR2026-06-0812 OK · 0 NOTE · 0 WARNING · 1 ERROR · 0 FAILURE
- OK2026-03-1014 OK · 0 NOTE · 0 WARNING · 0 ERROR · 0 FAILURE
Documentation
- Examples that run
- 4%
- Documented parameters
- 100%
- Return-value docs
- 100%
- References docs
- 30%
Downloads
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Repository practices
6 development-tooling and community-health practices detected across 5 families in the upstream repository
Checks run against github.com/piyalkarum/rcnv on 2026-07-19.
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Dependencies
Nothing depends on this yet.
Code & Tests
- Cyclomatic complexity
- 3.0 median / 23 max
Test coverage
Line coverage
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Tests / Examples
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Functions
51 24 exported
Complexity
6.2 avg / 23 max
Call network
51 nodes / 38 edges
Call graph
Open call graph →Lowest coverage
Per-function coverage is not measured for this package yet.
Datasets
People & History
4 releases. Pick two to compare their code metrics. R releases are shown for context.
Package metadata
- First published
- 2022-04-06
- Total releases
- 4 / 4 yrs
- License
- AGPL (>= 3) OSI
- Minimum R
- ≥ 3.6.0
- Bundled data
- 1.6 MB / 3 files
- Download size
- 2.6 MB
- Installed size
- not tracked yet
- With dependencies
- not tracked yet