The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants
Layla Aref, Lisa A. Bastarache, Jacob Hughey
The paper introduces the phers R package, which enables PheRS-based analysis of linked EHR and genetic data to study Mendelian disease and rare variants.
Bioinformatics · Sep 9, 2022Peer-reviewedBioinformatics