Bayesian hierarchical hypothesis testing in large-scale genome-wide association analysis.

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2024-11-19 DOI:10.1093/genetics/iyae164
Anirban Samaddar, Tapabrata Maiti, Gustavo de Los Campos
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引用次数: 0

Abstract

Variable selection and large-scale hypothesis testing are techniques commonly used to analyze high-dimensional genomic data. Despite recent advances in theory and methodology, variable selection and inference with highly collinear features remain challenging. For instance, collinearity poses a great challenge in genome-wide association studies involving millions of variants, many of which may be in high linkage disequilibrium. In such settings, collinearity can significantly reduce the power of variable selection methods to identify individual variants associated with an outcome. To address such challenges, we developed a Bayesian hierarchical hypothesis testing (BHHT)-a novel multiresolution testing procedure that offers high power with adequate error control and fine-mapping resolution. We demonstrate through simulations that the proposed methodology has a power-FDR performance that is competitive with (and in many scenarios better than) state-of-the-art methods. Finally, we demonstrate the feasibility of using BHHT with large sample size (n∼ 300,000) and ultra dimensional genotypes (∼ 15 million single-nucleotide polymorphisms or SNPs) by applying it to eight complex traits using data from the UK-Biobank. Our results show that the proposed methodology leads to many more discoveries than those obtained using traditional SNP-centered inference procedures. The article is accompanied by open-source software that implements the methods described in this study using algorithms that scale to biobank-size ultra-high-dimensional data.

大规模全基因组关联分析中的贝叶斯分层假设检验。
变量选择和大规模假设检验是分析高维基因组数据的常用技术。尽管最近在理论和方法上取得了进步,但变量选择和高度共线性特征的推断仍然具有挑战性。例如,在涉及数百万个变异体的全基因组关联研究中,共线性是一个巨大的挑战,其中许多变异体可能处于高度连锁不平衡状态。在这种情况下,共线性会大大降低变量选择方法识别与结果相关的个体变异的能力。为了应对这些挑战,我们开发了贝叶斯分层假设检验(BHHT)--一种新颖的多分辨率检验程序,它能在充分控制误差和精细映射分辨率的情况下提供高功率。我们通过仿真证明,所提出的方法的功率-FDR 性能可与最先进的方法相媲美(在许多情况下甚至优于)。最后,我们利用英国生物库的数据,将 BHHT 应用于八个复杂性状,证明了它在大样本量(n∼ 300,000)和超维基因型(1,500 万个单核苷酸多态性或 SNPs)条件下的可行性。结果表明,与传统的以 SNP 为中心的推断程序相比,我们提出的方法能带来更多的发现。文章附有开源软件,该软件使用可扩展到生物库规模的超高维数据的算法来实现本研究中描述的方法。
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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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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