ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies.
Eur J Hum Genet
; 31(3): 304-312, 2023 03.
Article
in En
| MEDLINE
| ID: mdl-36316489
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genome-Wide Association Study
/
DNA Copy Number Variations
Type of study:
Guideline
/
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Eur J Hum Genet
Journal subject:
GENETICA MEDICA
Year:
2023
Document type:
Article
Affiliation country:
United States
Country of publication:
United kingdom