Genotype Imputation and Population Genomics Efficiently from Variant Call Formatted (VCF) Files
Overview
Tools for efficient processing of large, whole genome genotype data sets in variant call format (VCF). It includes several functions to calculate commonly used population genomic metrics and a method for reference panel free genotype imputation, which is described in the preprint Gurke & Mayer (2024) doi:10.22541/au.172515591.10119928/v1.
Install
Health
- OK13 OK2026-08-05
- NOTE12 OK, 1 NOTE2026-08-01
- OK14 OK2026-03-10
Documentation
- Help pages
- 15 (2 internal)
- Examples that run
- 0%13 only when donttest examples are enabled (R CMD check --as-cran)
- Exported functions with examples
- 87%
- Documented parameters
- 99%
- Return-value docs
- 100%
- Help pages citing references
- 0%
- GenoPop HTML
Downloads
Dependencies
Installing GenoPop adds 14 packages (6 with compiled code, 6.3 MB of source tarballs). Heaviest: Rcpp 1.8 MB, RcppEigen 1.7 MB, rbibutils 1.1 MB. 3 more not on CRAN are not measured.
Code & Tests
People & History
Pick two releases to compare their code metrics.
- RR 4.6.0 released · 2026-04-24
- RR 4.5.0 released · 2025-04-11
- 1.0.0Latest
- 0.9.32024-09-11
- RR 4.4.0 released · 2024-04-24
Package metadata
- First published
- 2024-09-11
- Total releases
- 2 / 2 yrs
- License
- GPL (>= 3) OSI
- Download size
- 40 KB
Cite
Cite this package
Run in R for the authors' entry:
citation("GenoPop")The package provides a citation file, so citation() returns the authors' own entry.
It points to 10.22541/au.172515591.10119928/v1.
Cite the R Observatory
For a number measured here: a download total, a coverage figure, an archival date.
From data release v2026-10-23, which the citation names so these numbers can be found later. More on citing and the projects behind them.