Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases.
Nucleic Acids Res
; 50(6): e34, 2022 04 08.
Article
in En
| MEDLINE
| ID: mdl-34931221
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Variation
/
Software
/
Genetic Predisposition to Disease
/
Models, Genetic
Type of study:
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Nucleic Acids Res
Year:
2022
Document type:
Article