Literature DB >> 34788621

NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population.

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.
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

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


  6 in total

1.  Characterizing mobile element insertions in 5675 genomes.

Authors:  Yiwei Niu; Xueyi Teng; Honghong Zhou; Yirong Shi; Yanyan Li; Yiheng Tang; Peng Zhang; Huaxia Luo; Quan Kang; Tao Xu; Shunmin He
Journal:  Nucleic Acids Res       Date:  2022-03-21       Impact factor: 16.971

2.  SmProt: A Reliable Repository with Comprehensive Annotation of Small Proteins Identified from Ribosome Profiling.

Authors:  Yanyan Li; Honghong Zhou; Xiaomin Chen; Yu Zheng; Quan Kang; Di Hao; Lili Zhang; Tingrui Song; Huaxia Luo; Yajing Hao; Runsheng Chen; Peng Zhang; Shunmin He
Journal:  Genomics Proteomics Bioinformatics       Date:  2021-09-15       Impact factor: 6.409

3.  HKG: an open genetic variant database of 205 Hong Kong cantonese exomes.

Authors:  Min Ou; Henry Chi-Ming Leung; Amy Wing-Sze Leung; Ho-Ming Luk; Bin Yan; Chi-Man Liu; Tony Ming-For Tong; Myth Tsz-Shun Mok; Wallace Ming-Yuen Ko; Wai-Chun Law; Tak-Wah Lam; Ivan Fai-Man Lo; Ruibang Luo
Journal:  NAR Genom Bioinform       Date:  2022-02-08

4.  [Analysis of clinical significance and prognostic impact of TET2 single nucleotide polymorphism I1762V in patients with acute myeloid leukemia].

Authors:  Y W Li; Z Guo; L L Wang; L Zhou; X D Lyu; Y P Song
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2022-03-14

5.  Whole Exome Sequencing in South Africa: Stakeholder Views on Return of Individual Research Results and Incidental Findings.

Authors:  Nicole Van Der Merwe; Raj Ramesar; Jantina De Vries
Journal:  Front Genet       Date:  2022-06-08       Impact factor: 4.772

6.  TMC-SNPdb 2.0: an ethnic-specific database of Indian germline variants.

Authors:  Sanket Desai; Rohit Mishra; Suhail Ahmad; Supriya Hait; Asim Joshi; Amit Dutt
Journal:  Database (Oxford)       Date:  2022-05-11       Impact factor: 4.462

  6 in total

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