The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants - researchr publication

researchr

You are not signed in
Sign in
Sign up

Layla Aref, Lisa Bastarache, Jacob J. Hughey. The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants. Bioinformatics, 38(21):4972-4974, October 2022. [doi]

Abstract is missing.

runs on WebDSL