Statistical Methods for Modeling Polygenic Architecture in Association and Re-sequencing Studies

关联和重测序研究中多基因结构建模的统计方法

• 批准号: 9912184
• 负责人: Xiang Zhou
• 金额: $ 34万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-06-14 至 2022-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9912184
• 关键词: Address; Algorithms; Architecture; Base Sequence; Categories; Communities; Complex; Computer software; Data; Data Set; Development; Disease; Evaluation; Genetic; Genetic study; Health; Heritability; Human; Individual; Linkage Disequilibrium; Lipids; Logistics; Methods; Modeling; Non-Insulin-Dependent Diabetes Mellitus; Outcome; Pattern; Phenotype; Polygenic Traits; Research; Risk; Source; Statistical Methods; Structure; Testing; Variant; base; causal variant; disorder risk; flexibility; functional genomics; genetic architecture; genetic variant; genome sequencing; genome wide association study; improved; infancy; novel; open source; pleiotropism; population stratification; precision medicine; simulation; software development; statistics; success; tool; trait; user friendly software; user-friendly; whole genome

Project Summary Array- and sequencing-based association studies have identified many loci harboring genetic variants associated with complex traits and common diseases. Altogether, these associated variants only explain a small proportion of heritability, suggesting that most traits and diseases have a polygenic background and are influenced by many variants with small effects. Early attempts to model polygenic complex traits, notably via the linear mixed models (LMMs) and the best linear unbiased predictor (BLUP), have shown promising outcomes for estimating chip heritability, identifying causal variants, and predicting disease risks. However, statistical methods for modeling polygenic architecture remain in their infancy. In particular, existing methods rely on simple effect size assumptions, are not flexible nor adaptive to the underlying genetic architecture of a given trait or disease, and hence cannot take full advantage of the polygenic natural of most traits and diseases. To increase the power of association test and enable more precise phenotype and risk prediction, I propose to develop a suite of novel statistical methods to accurately and flexibly model the polygenic architecture. These new methods will facilitate evaluation and integration of variant functional annotations, multiple phenotype association mapping, and phenotype and risk prediction in association studies. In particular, we will (1) develop methods to evaluate and integrate variant genomic functional annotations to better understand the polygenic architecture of traits and diseases, and enable powerful association mapping; (2) develop strategies for association mapping with multiple correlated phenotypes to identify pleiotropic associations by taking advantage of the shared polygenic background among phenotypes; and (3) develop methods to flexibly model polygenic architecture and use all variants jointly to achieve accurate phenotype and risk prediction. We will develop efficient algorithms to accompany these methods and implement them in free open-source software. We will perform rigorous simulations and comparisons to evaluate our methods. Finally, we will perform in- depth analysis on several large-scale real data sets, including data from the Global Lipids Genetics Consortium, T2D-GENES and METSIM projects, to demonstrate the power of the proposed methods.

项目总结