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Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing.通过深度全基因组测序洞察38名南亚印度人的遗传结构和多样性。
PLoS Genet. 2014 May 15;10(5):e1004377. doi: 10.1371/journal.pgen.1004377. eCollection 2014 May.
3
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.全基因组跨种族荟萃分析为 2 型糖尿病易感性的遗传结构提供了新视角。
Nat Genet. 2014 Mar;46(3):234-44. doi: 10.1038/ng.2897. Epub 2014 Feb 9.
4
Comparing methods for performing trans-ethnic meta-analysis of genome-wide association studies.比较全基因组关联研究的跨种族荟萃分析方法。
Hum Mol Genet. 2013 Jun 1;22(11):2303-11. doi: 10.1093/hmg/ddt064. Epub 2013 Feb 12.
5
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans.一项针对角膜曲率的全基因组关联研究确定,血小板衍生生长因子受体α基因是欧洲白人眼睛大小的一个数量性状位点。
Mol Vis. 2013;19:243-53. Epub 2013 Jan 3.
6
Identification of a candidate gene for astigmatism.鉴定散光的候选基因。
Invest Ophthalmol Vis Sci. 2013 Feb 1;54(2):1260-7. doi: 10.1167/iovs.12-10463.
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Deep whole-genome sequencing of 100 southeast Asian Malays.对 100 名东南亚马来人进行深度全基因组测序。
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High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.利用电子病历对非裔美国人的 LDL 胆固醇进行高密度 GWAS 分析,揭示了 APOE 中的一个强保护性变异。
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10
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.通过跨种族荟萃分析发现和精细映射血清蛋白基因座。
Am J Hum Genet. 2012 Oct 5;91(4):744-53. doi: 10.1016/j.ajhg.2012.08.021. Epub 2012 Sep 27.

在不同亚洲人群中使用特定人群和全球通用的归因参考面板进行跨种族精细定位评估。

Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.

作者信息

Wang Xu, Cheng Ching-Yu, Liao Jiemin, Sim Xueling, Liu Jianjun, Chia Kee-Seng, Tai E-Shyong, Little Peter, Khor Chiea-Chuen, Aung Tin, Wong Tien-Yin, Teo Yik-Ying

机构信息

Saw Swee Hock School of Public Health, National University of Singapore, Singapore, Singapore.

Singapore Eye Research Institute, Singapore National Eye Center, Singapore, Singapore.

出版信息

Eur J Hum Genet. 2016 Apr;24(4):592-9. doi: 10.1038/ejhg.2015.150. Epub 2015 Jul 1.

DOI:10.1038/ejhg.2015.150
PMID:26130488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4929869/
Abstract

There has been limited success in identifying causal variants underlying association signals observed in genome-wide association studies (GWAS). The use of 1000 Genomes Project (1KGP) allows the imputation to estimate the genetic information at untyped variants. However, long stretches of high linkage disequilibrium within the genome prevent us from differentiating between causal variants and perfect surrogates, thus limiting our ability to identify causal variants. Transethnic strategies have been proposed as a possible solution to mitigate this. However, these studies generally rely on imputing genotypes from multiple ancestries from 1KGP but not against population-specific reference panels. Here, we perform the first transethnic fine-mapping study across three Asian cohorts from diverse ancestries at the loci implicated with eye and blood lipid traits, using population-specific reference panels that have been generated by whole-genome sequencing samples from the same ancestry groups. Our study outlines several challenges faced in a fine-mapping exercise where one simply aims to meta-analyse existing GWAS that have been imputed against reference haplotypes from the 1KGP.

摘要

在全基因组关联研究(GWAS)中,识别观察到的关联信号背后的因果变异的成功率有限。1000基因组计划(1KGP)的使用使得通过推断来估计未分型变异的遗传信息成为可能。然而,基因组内长片段的高度连锁不平衡使我们无法区分因果变异和完美替代物,从而限制了我们识别因果变异的能力。跨种族策略已被提议作为减轻这一问题的可能解决方案。然而,这些研究通常依赖于从1KGP推断多个祖先的基因型,而不是针对特定人群的参考面板。在这里,我们使用由来自相同祖先群体的全基因组测序样本生成的特定人群参考面板,对来自不同祖先的三个亚洲队列中与眼睛和血脂性状相关的位点进行了首次跨种族精细定位研究。我们的研究概述了在精细定位过程中面临的几个挑战,在这个过程中,人们只是简单地对已经根据1KGP的参考单倍型推断出的现有GWAS进行荟萃分析。