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ibdfindr: HMM Toolkit for Inferring IBD Segments from SNP Genotypes

Implements continuous-time hidden Markov models (HMMs) to infer identity-by-descent (IBD) segments shared by two individuals from their single-nucleotide polymorphism (SNP) genotypes. Provides posterior probabilities at each marker (forward-backward algorithm), prediction of IBD segments (Viterbi algorithm), and functions for visualising results. Supports both autosomal data and X-chromosomal data.

Version:0.3.1
Depends:R (≥ 4.2)
Imports:forrel,ggplot2,ibdsim2,pedtools,ribd
Suggests:testthat (≥ 3.0.0)
Published:2025-08-18
DOI:10.32614/CRAN.package.ibdfindr
Author:Magnus Dehli VigelandORCID iD [aut, cre]
Maintainer:Magnus Dehli Vigeland <m.d.vigeland at medisin.uio.no>
BugReports:https://github.com/magnusdv/ibdfindr/issues
License:GPL (≥ 3)
URL:https://github.com/magnusdv/ibdfindr
NeedsCompilation:no
Language:en-GB
Materials:README,NEWS
CRAN checks:ibdfindr results

Documentation:

Reference manual:ibdfindr.html ,ibdfindr.pdf

Downloads:

Package source: ibdfindr_0.3.1.tar.gz
Windows binaries: r-devel:ibdfindr_0.3.1.zip, r-release:ibdfindr_0.3.1.zip, r-oldrel:ibdfindr_0.3.1.zip
macOS binaries: r-release (arm64):ibdfindr_0.3.1.tgz, r-oldrel (arm64):ibdfindr_0.3.1.tgz, r-release (x86_64):ibdfindr_0.3.1.tgz, r-oldrel (x86_64):ibdfindr_0.3.1.tgz

Reverse dependencies:

Reverse imports:pedsuite

Linking:

Please use the canonical formhttps://CRAN.R-project.org/package=ibdfindrto link to this page.


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