Open AccessIdentification of clinically actionable secondary genetic variants from whole‐genome sequencing in a large‐scale Chinese population
Author(s) -
Cong PeiKuan,
Khederzadeh Saber,
Yuan ChengDa,
Ma RuiJie,
Zhang YiYao,
Liu JunQuan,
Yu ShiHui,
Xu Lin,
Gao JianHua,
Pan HongXu,
Li JinChen,
Xie ShuYang,
Liu KeQi,
Tang BeiSha,
Zheng HouFeng
Publication year - 2022
Publication title -
clinical and translational medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 1
ISSN - 2001-1326
DOI - 10.1002/ctm2.866
Subject(s) - genetics , exome sequencing , dna sequencing , biology , mendelian inheritance , medical genetics , genomics , whole genome sequencing , exome , population , human genetics , 1000 genomes project , gene , genome , medicine , single nucleotide polymorphism , genotype , mutation , environmental health