Uses read counts for biallelic single nucleotide polymorphisms (SNPs) to compare the likelihoods for the observed read counts given that a sample is either diploid or triploid. It allows parameters to be specified to account for sequencing error rates and allelic bias. For details of the algorithm, please see Delomas (2019) <doi:10.1111/1755-0998.13073>.
|Author||Thomas Delomas [aut, cre]|
|Maintainer||Thomas Delomas <email@example.com>|
|License||MIT + file LICENSE|
|Package repository||View on CRAN|
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