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, 2022 10 31.
Article
in En
| MEDLINE
| ID: mdl-36083022
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Software
/
Electronic Health Records
Type of study:
Etiology_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Bioinformatics
Journal subject:
INFORMATICA MEDICA
Year:
2022
Type:
Article
Affiliation country:
United States