| Literature DB >> 34788621 |
Peng Zhang1, Huaxia Luo1, Yanyan Li2, You Wang3, Jiajia Wang4, Yu Zheng4, Yiwei Niu4, Yirong Shi5, Honghong Zhou1, Tingrui Song1, Quan Kang1, Tao Xu6, Shunmin He7.
Abstract
The lack of haplotype reference panels and whole-genome sequencing resources specific to the Chinese population has greatly hindered genetic studies in the world's largest population. Here, we present the NyuWa genome resource, based on deep (26.2×) sequencing of 2,999 Chinese individuals, and construct a NyuWa reference panel of 5,804 haplotypes and 19.3 million variants, which is a high-quality publicly available Chinese population-specific reference panel with thousands of samples. Compared with other panels, the NyuWa reference panel reduces the Han Chinese imputation error rate by a margin ranging from 30% to 51%. Population structure and imputation simulation tests support the applicability of one integrated reference panel for northern and southern Chinese. In addition, a total of 22,504 loss-of-function variants in coding and noncoding genes are identified, including 11,493 novel variants. These results highlight the value of the NyuWa genome resource in facilitating genetic research in Chinese and Asian populations.Entities:
Keywords: Chinese population; genome resource; haplotype reference panel; variants; whole genome sequencing
Mesh:
Year: 2021 PMID: 34788621 DOI: 10.1016/j.celrep.2021.110017
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423