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The ChinaMAP reference panel for the accurate genotype imputation in Chinese populations.

作者信息

Li Lin, Huang Peide, Sun Xiaohui, Wang Siyu, Xu Min, Liu Sha, Feng Zhimin, Zhang Qing, Wang Xiaoji, Zheng Xiaole, Dai Mengyao, Bi Yufang, Ning Guang, Cao Yanan, Wang Weiqing

机构信息

Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, National Clinical Research Centre for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission, State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

National Research Center for Translational Medicine, National Key Scientific Infrastructure for Translational Medicine, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Cell Res. 2021 Dec;31(12):1308-1310. doi: 10.1038/s41422-021-00564-z. Epub 2021 Sep 6.

DOI:10.1038/s41422-021-00564-z
PMID:34489580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8648815/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/718d/8648815/ae3046abc900/41422_2021_564_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/718d/8648815/ae3046abc900/41422_2021_564_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/718d/8648815/ae3046abc900/41422_2021_564_Fig1_HTML.jpg

相似文献

[1]
The ChinaMAP reference panel for the accurate genotype imputation in Chinese populations.

Cell Res. 2021-12

[2]
NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants.

Genome Med. 2019-10-22

[3]
NyuWa Genome resource: A deep whole-genome sequencing-based variation profile and reference panel for the Chinese population.

Cell Rep. 2021-11-16

[4]
Validation of genotype imputation in Southeast Asian populations and the effect of single nucleotide polymorphism annotation on imputation outcome.

BMC Med Genet. 2018-2-13

[5]
Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank Project.

BMC Genomics. 2018-7-24

[6]
Genotype imputation for Han Chinese population using Haplotype Reference Consortium as reference.

Hum Genet. 2018-5-31

[7]
Genotype-imputation accuracy across worldwide human populations.

Am J Hum Genet. 2009-2

[8]
Novel susceptibility loci were found in Chinese genetic generalized epileptic patients by genome-wide association study.

CNS Neurosci Ther. 2014-11

[9]
Japonica Array NEO with increased genome-wide coverage and abundant disease risk SNPs.

J Biochem. 2021-10-12

[10]
Lack of association between the BDNF C270T polymorphism and schizophrenia in a Chinese Han population.

Schizophr Res. 2007-12

引用本文的文献

[1]
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Transl Psychiatry. 2025-8-19

[2]
Bioinformatic insights into five Chinese population substructures inferred from the East Asian-specific AISNP panel.

BMC Genomics. 2025-8-18

[3]
Machine learning models for pharmacogenomic variant effect predictions - recent developments and future frontiers.

Pharmacogenomics. 2025

[4]
Sleep Phenotypes, Genetic Susceptibility, and Risk of Obesity in Patients With Type 2 Diabetes: A National Prospective Cohort Study.

J Diabetes. 2025-5

[5]
Distinct methylomic signatures of high-altitude acclimatization and adaptation in the Tibetan Plateau.

Cell Discov. 2025-5-6

[6]
SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populations.

Nat Commun. 2024-12-30

[7]
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population.

Commun Biol. 2024-12-19

[8]
Association of single nucleotide polymorphisms and gene-environment interactions with major depressive disorder in Chinese.

Heliyon. 2024-9-5

[9]
Imputation accuracy across global human populations.

Am J Hum Genet. 2024-5-2

[10]
Reconstruction of private genomes through reference-based genotype imputation.

Genome Biol. 2023-12-6

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