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, or genotypes sampled from those probabilties, can then be exported
for downstream analysis. 'polyRAD' is described by Clark et al. (2018)
|Author||Lindsay V. Clark [aut, cre] (<https://orcid.org/0000-0002-3881-9252>), U.S. National Science Foundation [fnd]|
|Maintainer||Lindsay V. Clark <[email protected]>|
|License||GPL (>= 2)|
|Package repository||View on GitHub|
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