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本文引用的文献

1
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.利用高密度基因分型和胰岛特异性表观基因组图谱对 2 型糖尿病位点进行精细映射到单变体分辨率。
Nat Genet. 2018 Nov;50(11):1505-1513. doi: 10.1038/s41588-018-0241-6. Epub 2018 Oct 8.
2
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.12940 例 2 型糖尿病病例和对照的序列数据和关联统计数据。
Sci Data. 2017 Dec 19;4:170179. doi: 10.1038/sdata.2017.179.
3
Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution.考虑祖先因素的全基因组关联研究的跨种族元回归增加了发现的效力并提高了精细定位分辨率。
Hum Mol Genet. 2017 Sep 15;26(18):3639-3650. doi: 10.1093/hmg/ddx280.
4
Reference-based phasing using the Haplotype Reference Consortium panel.使用单倍型参考联盟面板进行基于参考的定相
Nat Genet. 2016 Nov;48(11):1443-1448. doi: 10.1038/ng.3679. Epub 2016 Oct 3.
5
Next-generation genotype imputation service and methods.下一代基因型填充服务和方法。
Nat Genet. 2016 Oct;48(10):1284-1287. doi: 10.1038/ng.3656. Epub 2016 Aug 29.
6
A reference panel of 64,976 haplotypes for genotype imputation.用于基因型插补的64976个单倍型参考面板。
Nat Genet. 2016 Oct;48(10):1279-83. doi: 10.1038/ng.3643. Epub 2016 Aug 22.
7
A novel random effect model for GWAS meta-analysis and its application to trans-ethnic meta-analysis.一种用于全基因组关联研究荟萃分析的新型随机效应模型及其在跨种族荟萃分析中的应用。
Biometrics. 2016 Sep;72(3):945-54. doi: 10.1111/biom.12481. Epub 2016 Feb 24.
8
A global reference for human genetic variation.人类遗传变异的全球参考。
Nature. 2015 Oct 1;526(7571):68-74. doi: 10.1038/nature15393.
9
Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study.在高度混合的多民族人群中开展全基因组关联研究面临的挑战:Generation R研究
Eur J Epidemiol. 2015 Apr;30(4):317-30. doi: 10.1007/s10654-015-9998-4. Epub 2015 Mar 12.
10
Second-generation PLINK: rising to the challenge of larger and richer datasets.第二代PLINK:应对更大、更丰富数据集的挑战
Gigascience. 2015 Feb 25;4:7. doi: 10.1186/s13742-015-0047-8. eCollection 2015.

跨种族代谢综合征的多民族研究荟萃分析。

Transethnic meta-analysis of metabolic syndrome in a multiethnic study.

机构信息

Department of Mathematical and Statistical Sciences, University of Colorado Denver, Denver, Colorado.

Department of Epidemiology, University of California Irvine, Irvine, California.

出版信息

Genet Epidemiol. 2020 Jan;44(1):16-25. doi: 10.1002/gepi.22267. Epub 2019 Oct 24.

DOI:10.1002/gepi.22267
PMID:31647587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6986323/
Abstract

Genome-wide association studies (GWAS) have been used to establish thousands of genetic associations across numerous phenotypes. To improve the power of GWAS and generalize associations across ethnic groups, transethnic meta-analysis methods are used to combine the results of several GWAS from diverse ancestries. The goal of this study is to identify genetic associations for eight quantitative metabolic syndrome (MetS) traits through a meta-analysis across four ethnic groups. Traits were measured in the GENetics of Noninsulin dependent Diabetes Mellitus (GENNID) Study which consists of African-American (families = 73, individuals = 288), European-American (families = 79, individuals = 519), Japanese-American (families = 17, individuals = 132), and Mexican-American (families = 113, individuals = 610) samples. Genome-wide association results from these four ethnic groups were combined using four meta-analysis methods: fixed effects, random effects, TransMeta, and MR-MEGA. We provide an empirical comparison of the four meta-analysis methods from the GENNID results, discuss which types of loci (characterized by allelic heterogeneity) appear to be better detected by each of the four meta-analysis methods in the GENNID Study, and validate our results using previous genetic discoveries. We specifically compare the two transethnic methods, TransMeta and MR-MEGA, and discuss how each transethnic method's framework relates to the types of loci best detected by each method.

摘要

全基因组关联研究(GWAS)已被用于在众多表型中建立数千个遗传关联。为了提高 GWAS 的效力并将关联推广到不同的种族群体,跨种族荟萃分析方法被用于结合来自不同种族的多个 GWAS 的结果。本研究的目的是通过对四个种族的荟萃分析,确定八个定量代谢综合征(MetS)特征的遗传关联。在由非胰岛素依赖型糖尿病遗传研究(GENNID)组成的研究中测量了特征,该研究包括非裔美国人(家庭=73,个体=288)、欧洲裔美国人(家庭=79,个体=519)、日裔美国人(家庭=17,个体=132)和墨西哥裔美国人(家庭=113,个体=610)样本。使用四种荟萃分析方法:固定效应、随机效应、TransMeta 和 MR-MEGA,对这四个种族的全基因组关联结果进行了组合。我们从 GENNID 结果中对这四种荟萃分析方法进行了实证比较,讨论了哪些类型的位点(特征是等位基因异质性)似乎更能被 GENNID 研究中的四种荟萃分析方法中的每一种检测到,并使用以前的遗传发现验证了我们的结果。我们特别比较了两种跨种族方法,TransMeta 和 MR-MEGA,并讨论了每种跨种族方法的框架如何与每种方法最佳检测到的位点类型相关。