通过 Haseman-Elston 回归得出遗传率的置信区间。

Pub Date : 2017-09-26 DOI:10.1515/sagmb-2016-0076
Tamar Sofer
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摘要

遗传率是指群体中表型变异可归因于个体基因型的比例。遗传率在进化生物学和医学中都被认为是一个重要的衡量指标,在遗传流行病学研究中被常规估算和报告。在基于人群的全基因组关联研究(GWAS)中,使用混合模型来估计方差分量,并从中得到遗传率估计值。估计的遗传率是由遗传亲缘关系矩阵(从基因型测得的亲缘关系)引起的模型总方差的比例。目前的做法是使用引导法(速度较慢)或正态渐近法来估计遗传率估计值的精度;然而,这种近似方法在参数空间的边界附近或样本量较小时不能成立。在本文中,我们建议通过 Haseman-Elston 回归估计方差分量,找到方差分量和方差比例的渐近分布,并利用它们构建置信区间(CI)。我们的方法得到了进一步发展,可以通过元分析多项研究的信息来获得无偏的方差分量估计值并构建置信区间。我们在西班牙裔社区健康研究/拉美裔研究(HCHS/SOL)的数据中演示了我们的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Confidence intervals for heritability via Haseman-Elston regression.

Heritability is the proportion of phenotypic variance in a population that is attributable to individual genotypes. Heritability is considered an important measure in both evolutionary biology and in medicine, and is routinely estimated and reported in genetic epidemiology studies. In population-based genome-wide association studies (GWAS), mixed models are used to estimate variance components, from which a heritability estimate is obtained. The estimated heritability is the proportion of the model's total variance that is due to the genetic relatedness matrix (kinship measured from genotypes). Current practice is to use bootstrapping, which is slow, or normal asymptotic approximation to estimate the precision of the heritability estimate; however, this approximation fails to hold near the boundaries of the parameter space or when the sample size is small. In this paper we propose to estimate variance components via a Haseman-Elston regression, find the asymptotic distribution of the variance components and proportions of variance, and use them to construct confidence intervals (CIs). Our method is further developed to obtain unbiased variance components estimators and construct CIs by meta-analyzing information from multiple studies. We demonstrate our approach on data from the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).

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