首页> 美国卫生研究院文献>Frontiers in Genetics >Capitalizing on Admixture in Genome-Wide Association Studies: A Two-Stage Testing Procedure and Application to Height in African-Americans
【2h】

Capitalizing on Admixture in Genome-Wide Association Studies: A Two-Stage Testing Procedure and Application to Height in African-Americans

机译:在全基因组关联研究中利用混合物:两阶段测试程序及其对非洲裔美国人身高的应用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

As genome-wide association studies expand beyond populations of European ancestry, the role of admixture will become increasingly important in the continued discovery and fine-mapping of variation influencing complex traits. Although admixture is commonly viewed as a confounding influence in association studies, approaches such as admixture mapping have demonstrated its ability to highlight disease susceptibility regions of the genome. In this study, we illustrate a powerful two-stage testing strategy designed to uncover trait-associated single nucleotide polymorphisms in the presence of ancestral allele frequency differentiation. In the first stage, we conduct an association scan by using predicted genotypic values based on regional admixture estimates. We then select a subset of promising markers for inclusion in a second-stage analysis, where association is tested between the observed genotype and the phenotype conditional on the predicted genotype. We prove that, under the null hypothesis, the test statistics used in each stage are orthogonal and asymptotically independent. Using simulated data designed to mimic African-American populations in the case of a quantitative trait, we show that our two-stage procedure maintains appropriate control of the family wise error rate and has higher power under realistic effect sizes than the one-stage testing procedure in which all markers are tested for association simultaneously with control of admixture. We apply the proposed procedure to a study of height in 201 African-Americans genotyped at 108 ancestry informative markers. The two-stage procedure identified two statistically significant markers rs1985080 (PTHB1/BBS9) and rs952718 (ABCA12). PTHB1/BBS9 is downregulated by parathyroid hormone in osteoblastic cells and is thought to be involved in parathyroid hormone action in bones and may play a role in height. ABCA12 is a member of the superfamily of ATP binding cassette transporters and its potential involvement in height is unclear.
机译:随着全基因组关联研究的范围扩展到欧洲血统的范围之外,在继续发现和精细映射影响复杂性状的变异中,混合物的作用将变得越来越重要。尽管在关联研究中通常将混合物视为混杂因素,但诸如混合物作图的方法已证明其具有突出基因组疾病易感性区域的能力。在这项研究中,我们说明了一个强大的两阶段测试策略,旨在发现祖先等位基因频率差异时发现与性状相关的单核苷酸多态性。在第一阶段,我们使用基于区域混合物估计值的预测基因型值进行关联扫描。然后,我们选择一个有前途的标记子集,以包括在第二阶段分析中,在该阶段中,将测试观察到的基因型与以预测基因型为条件的表型之间的关联。我们证明,在零假设下,每个阶段使用的检验统计量是正交的,并且是渐近独立的。使用旨在模拟定量特征情况下的非裔美国人群体的模拟数据,我们表明,与一阶段测试程序相比,我们的两阶段程序可以保持对家庭明智错误率的适当控制,并且在实际效应大小下具有更高的功效其中所有标记物均在混合剂控制下同时进行缔合测试。我们将拟议的程序应用于研究108个祖先信息标记基因型的201名非裔美国人的身高。两阶段程序确定了两个具有统计意义的标记rs1985080(PTHB1 / BBS9)和rs952718(ABCA12)。 PTHB1 / BBS9在成骨细胞中被甲状旁腺激素下调,被认为与骨骼中甲状旁腺激素的作用有关,并可能在身高中起作用。 ABCA12是ATP结合盒转运蛋白超家族的成员,其潜在参与的身高尚不清楚。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号