Nothing
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>.
Package details |
|
---|---|
Author | Thomas Delomas [aut, cre] |
Maintainer | Thomas Delomas <thomas.delomas@idfg.idaho.gov> |
License | MIT + file LICENSE |
Version | 0.1.0 |
URL | https://github.com/delomast/tripsAndDipR |
Package repository | View on CRAN |
Installation |
Install the latest version of this package by entering the following in R:
|
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.