knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "README-" )
This is the original code for the updog procedure. To use the new updog package, please see here.
This package will fit an empirical Bayesian procedure to genotype autopolyploid individuals from reduced-representation next-generation sequencing (NGS) data, such as genotyping by sequencing (GBS) [@elshire2011robust] or restriction site-associated DNA sequencing (RAD-Seq) [@baird2008rapid]. For such NGS data there exist other methods for genotyping --- see for example ebg [@blischak2017snp] and TET [@maruki2017genotype]. updog
adds to this field by:
plot.updog
).summary.updog
).rupdog
).We've included a few SNP's from the data of @shirasawa2017high to show off the features of updog
. See snpdata
.
A vignette is available here.
Please report any bugs/issues here.
To install, run the following code in R: ``` {r, eval = FALSE}
devtools::install_github("dcgerard/updog")
# Citation If you find the methods in this package useful, please cite > Gerard, D., Ferrão L.F.V., Garcia, A.A.F., & Stephens, M. (2018). Harnessing Empirical Bayes and Mendelian Segregation for Genotyping Autopolyploids from Messy Sequencing Data. *bioRxiv*. doi: [10.1101/281550](https://doi.org/10.1101/281550). Or, using BibTex: ``` tex @article {gerard2018harnessing, author = {Gerard, David and Ferr{\~a}o, Luis Felipe Ventorim and Garcia, Antonio Augusto Franco and Stephens, Matthew}, title = {Harnessing Empirical Bayes and Mendelian Segregation for Genotyping Autopolyploids from Messy Sequencing Data}, year = {2018}, doi = {10.1101/281550}, publisher = {Cold Spring Harbor Laboratory}, URL = {https://www.biorxiv.org/content/early/2018/03/16/281550}, eprint = {https://www.biorxiv.org/content/early/2018/03/16/281550.full.pdf}, journal = {bioRxiv} }
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.