phers: Calculate Phenotype Risk Scores

Use phenotype risk scores based on linked clinical and genetic data to study Mendelian disease and rare genetic variants. See Bastarache et al. 2018 <doi:10.1126/science.aal4043>.

Getting started

Package details

AuthorJake Hughey [aut, cre], Layla Aref [aut]
MaintainerJake Hughey <jakejhughey@gmail.com>
LicenseGPL-2
Version1.0.2
URL https://phers.hugheylab.org https://github.com/hugheylab/phers
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("phers")

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phers documentation built on March 31, 2023, 5:43 p.m.