Open AccessThe phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants
Author(s) -
Layla Aref,
Lisa Bastarache,
Jacob Hughey
Publication year - 2022
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btac619
Subject(s) - mendelian inheritance , computational biology , omim : online mendelian inheritance in man , biobank , computer science , phenotype , biology , genetics , gene
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