Package: polyRAD Version: 2.0.1 Date: 2026-03-21 Title: Genotype Calling with Uncertainty from Sequencing Data in Polyploids and Diploids Authors@R: c(person("Lindsay V.", "Clark", email = "Lindsay.Clark@seattlechildrens.org", role = c("aut", "cre"), comment = c(ORCID = "0000-0002-3881-9252")), person("U.S. National Science Foundation", role = "fnd")) Author: Lindsay V. Clark [aut, cre] (), U.S. National Science Foundation [fnd] Maintainer: Lindsay V. Clark Depends: R (>= 3.5.0), methods Imports: fastmatch, pcaMethods, Rcpp, stringi Suggests: rrBLUP, Rsamtools, GenomeInfoDb, Biostrings, GenomicRanges, VariantAnnotation, SummarizedExperiment, S4Vectors, IRanges, BiocGenerics, knitr, rmarkdown, GenomicFeatures, ggplot2, adegenet, txdbmaker, polymapR, BSgenome LinkingTo: Rcpp VignetteBuilder: knitr, rmarkdown Description: Read depth data from genotyping-by-sequencing (GBS) or restriction site-associated DNA sequencing (RAD-seq) are imported and used to make Bayesian probability estimates of genotypes in polyploids or diploids. The genotype probabilities, posterior mean genotypes, or most probable genotypes can then be exported for downstream analysis. 'polyRAD' is described by Clark et al. (2019) , and the Hind/He statistic for marker filtering is described by Clark et al. (2022) . A variant calling pipeline for highly duplicated genomes is also included and is described by Clark et al. (2020, Version 1) . License: GPL (>= 2) URL: https://github.com/lvclark/polyRAD Config/pak/sysreqs: libicu-dev Repository: https://lvclark.r-universe.dev Date/Publication: 2026-03-22 00:34:31 UTC RemoteUrl: https://github.com/lvclark/polyRAD RemoteRef: HEAD RemoteSha: 4408d65bfd59b2d643d26eb869339348be61b13e NeedsCompilation: yes Packaged: 2026-06-24 11:00:34 UTC; root