BIGr
0.7.2Breeding Insight Genomics Functions for Polyploid and Diploid Species
Overview
Functions developed within Breeding Insight to analyze diploid and polyploid breeding and genetic data. 'BIGr' provides the ability to filter variant call format (VCF) files, extract single nucleotide polymorphisms (SNPs) from diversity arrays technology missing allele discovery count (DArT MADC) files, and manipulate genotype data for both diploid and polyploid species. It also serves as the core dependency for the 'BIGapp' 'Shiny' app, which provides a user-friendly interface for performing routine genotype analysis tasks such as dosage calling, filtering, principal component analysis (PCA), genome-wide association studies (GWAS), and genomic prediction. For more details about the included 'breedTools' functions, see Funkhouser et al. (2017) <doi:10.2527/tas2016.0003>, and the 'updog' output format, see Gerard et al. (2018) <doi:10.1534/genetics.118.301468>.
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Health
- ERROR r-oldrel-macos-x86_64
- ERROR2026-03-1011 OK · 0 NOTE · 0 WARNING · 3 ERROR · 0 FAILURE
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Code & tests
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Functions
37 24 exported
Complexity
14.4 avg / 63 max
Call network
37 nodes / 28 edges
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People & History
3 releases. Pick two to compare their code metrics; R releases are shown for context.
- 0.7.2Latest2026-05-18 · current release
- RR 4.6.0 released · 2026-04-24
- 0.6.22025-09-18 · diff ↗
- 0.5.52025-05-19
Package metadata
- First published
- 2025-05-19
- Total releases
- 3 / 1 yrs
- License
- Apache License (>= 2)
- Download size
- not tracked yet
- Installed size
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- With dependencies
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