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基于家系的全基因组关联研究设计,以提高效能和稳健性。

Family-based genome-wide association study designs for increased power and robustness.

作者信息

Guan Junming, Tan Tammy, Nehzati Seyed Moeen, Bennett Michael, Turley Patrick, Benjamin Daniel J, Young Alexander Strudwick

机构信息

UCLA Anderson School of Management, Los Angeles, CA, USA.

National Bureau of Economic Research, Cambridge, MA, USA.

出版信息

Nat Genet. 2025 Apr;57(4):1044-1052. doi: 10.1038/s41588-025-02118-0. Epub 2025 Mar 10.

Abstract

Family-based genome-wide association studies (FGWASs) use random, within-family genetic variation to remove confounding from estimates of direct genetic effects (DGEs). Here we introduce a 'unified estimator' that includes individuals without genotyped relatives, unifying standard and FGWAS while increasing power for DGE estimation. We also introduce a 'robust estimator' that is not biased in structured and/or admixed populations. In an analysis of 19 phenotypes in the UK Biobank, the unified estimator in the White British subsample and the robust estimator (applied without ancestry restrictions) increased the effective sample size for DGEs by 46.9% to 106.5% and 10.3% to 21.0%, respectively, compared to using genetic differences between siblings. Polygenic predictors derived from the unified estimator demonstrated superior out-of-sample prediction ability compared to other family-based methods. We implemented the methods in the software package snipar in an efficient linear mixed model that accounts for sample relatedness and sibling shared environment.

摘要

基于家系的全基因组关联研究(FGWASs)利用家系内的随机遗传变异来消除直接遗传效应(DGEs)估计中的混杂因素。在此,我们引入一种“统一估计器”,它纳入了没有基因分型亲属的个体,将标准方法和FGWAS统一起来,同时提高了DGE估计的效能。我们还引入了一种“稳健估计器”,它在结构化和/或混合人群中不会产生偏差。在对英国生物银行中19种表型的分析中,与使用兄弟姐妹之间的遗传差异相比,英国白人子样本中的统一估计器和稳健估计器(不受祖先限制应用)分别将DGEs的有效样本量提高了46.9%至106.5%和10.3%至21.0%。与其他基于家系的方法相比,从统一估计器得出的多基因预测因子表现出卓越的样本外预测能力。我们在软件包snipar中以一种考虑样本相关性和兄弟姐妹共享环境的高效线性混合模型实现了这些方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ae/11985344/0e0edfb8bbdf/41588_2025_2118_Fig1_HTML.jpg

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