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Statistical methods for genetic association studies: Multi-cohort and rare genetic variants approaches.

机译:遗传关联研究的统计方法:多队列和稀有遗传变异方法。

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摘要

Genetic association studies have successfully identified many genetic markers associated with complex human diseases and related quantitative traits. However, for most complex diseases and quantitative traits, all associated genetic markers identified to date only explain a small proportion of heritability. Thus, exploring the unexplained heritability in these traits will help us discover novel genetic determinants for these traits and better understand disease etiology and pathophysiology. Due to limited sample size, a single cohort study may not have sufficient power to identify novel genetic association with a small effect size, and meta-analysis approaches have been proposed and applied to combine results from multiple cohorts in large consortia, increasing the sample size and statistical power. Rare genetic variants and gene by environment interaction may both play a role in genetic association studies. In this dissertation, we develop statistical methods in meta-analysis, rare genetic variants analysis and gene by environment interaction analysis, conduct extensive simulation studies, and apply these methods in real data examples. First, we develop a method of moments estimator for the between-study covariance matrix in random effects model multivariate meta-analysis. Our estimator is the first such estimator in matrix form, and holds the invariance property to linear transformations. It has similar performance with existing methods in simulation studies and real data analysis. Next, we extend the Sequence Kernel Association Test (SKAT), a rare genetic variants analysis approach for unrelated individuals, to be applicable in family samples for quantitative traits. The extension is necessary, as the original test has inflated type I error when directly applied to related individuals, and selecting an unrelated subset from family samples reduces the sample size and power. Finally, we derive methods for rare genetic variants analysis in detecting gene by environment interaction on quantitative traits, in the context of univariate test on the interaction term parameter. We develop statistical tests in the settings of both burden test and SKAT, for both unrelated and related individuals. Our methods are relevant to genetic association studies, and we hope that they can facilitate research in this field and beyond.
机译:遗传关联研究已成功鉴定出许多与复杂人类疾病和相关定量性状相关的遗传标记。然而,对于大多数复杂的疾病和数量性状,迄今为止确定的所有相关遗传标记仅能解释一小部分遗传力。因此,探索这些性状的无法解释的遗传力将有助于我们发现这些性状的新颖遗传决定因素,并更好地了解疾病的病因和病理生理。由于样本量有限,单个队列研究可能没有足够的能力来鉴定具有较小效应量的新型遗传关联,因此提出了荟萃分析方法,并将其应用于合并大联盟中多个队列的结果,从而增加了样本量和统计能力。罕见的遗传变异和环境相互作用下的基因都可能在遗传关联研究中发挥作用。本文开发了环境分析的荟萃分析,稀有遗传变异分析和基因统计方法,进行了广泛的模拟研究,并将这些方法应用于实际数据实例。首先,我们为随机效应模型多元荟萃分析中的研究间协方差矩阵开发了矩估计方法。我们的估计器是矩阵形式的第一个此类估计器,并且具有线性变换的不变性。在仿真研究和真实数据分析中,它具有与现有方法相似的性能。接下来,我们扩展了序列内核关联测试(SKAT),这是一种针对无关个体的罕见遗传变异分析方法,适用于定量特征的家庭样品。扩展是必要的,因为当直接应用于相关个体时,原始测试会增加I型错误,并且从家庭样本中选择不相关的子集会减少样本数量和功效。最后,在单项检验相互作用项参数的背景下,我们得出了通过环境对数量性状的相互作用进行基因检测的稀有遗传变异分析方法。我们针对无关人员和相关人员在负担测试和SKAT设置中开发统计测试。我们的方法与遗传关联研究相关,我们希望它们可以促进该领域及以后的研究。

著录项

  • 作者

    Chen, Han.;

  • 作者单位

    Boston University.;

  • 授予单位 Boston University.;
  • 学科 Biology Biostatistics.;Biology Genetics.;Statistics.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 138 p.
  • 总页数 138
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:41:45

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