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A Unified Framework for Detecting Genetic Association with Multiple SNPs in a Candidate Gene or Region: Contrasting Genotype Scores and LD Patterns between Cases and Controls

机译:用于检测候选基因或区域中多个SNP的遗传关联的统一框架:病例和对照之间的基因型评分和LD模式对比

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摘要

It is critical to develop and apply powerful statistical tests for genetic association studies due to typically weak associations with complex human diseases or phenotypes. For population-based case-control studies with unphased multilocus genotype data, most of the existing methods are based on comparing genotype scores, e.g. allele frequencies, between the case and control groups. Another class of approaches are motivated to contrast linkage disequilibrium (LD) patterns between the two groups. It is expected that no single test can be uniformly most powerful across all situations, and different tests may perform better under different scenarios. A recent effort has been devoted to combining the above two classes of approaches, which however has some potential drawbacks. Here we propose a general and simple framework to unify the above two classes of approaches: it is based on the simple idea to incorporate LD measurements, in addition to genotype scores, as covariates in a logistic regression model, from which various tests can be constructed by taking advantage of the nice properties of the score statistics for the logistic model. It also has an advantage in easily accommodating covariates and other study designs. We use simulated data to show that our proposed tests performed well across several scenarios. In particular, in contrast to either of the two classes of the tests that is only powerful in detecting only one, but not both, of the two types of the distributional differences between cases and controls, our proposed tests are sensitive to both.
机译:由于与复杂人类疾病或表型的关联通常较弱,因此开发强大的统计检验并将其应用于遗传关联研究至关重要。对于具有无阶段多基因座基因型数据的基于人群的病例对照研究,大多数现有方法都基于比较基因型评分,例如病例组和对照组之间的等位基因频率。另一类方法旨在激发两组之间的对比连锁不平衡(LD)模式。可以预期,在任何情况下,没有一个单一的测试可以在所有情况下都具有最强大的功能,并且不同的测试在不同的情况下可能会表现更好。最近致力于将上述两类方法结合起来,但是,这有一些潜在的缺点。在这里,我们提出一个通用且简单的框架来统一上述两类方法:它基于简单的思想,除了将基因型评分之外,还将LD测量值作为对数回归模型中的协变量,可以从中构建各种检验通过利用逻辑模型得分统计的良好属性。它在易于容纳协变量和其他研究设计方面也具有优势。我们使用模拟数据表明,我们提出的测试在多种情况下均表现良好。尤其是,与仅能检测案例和控件之间的两种类型的分布差异中的一种(但不能检测两种)的两种测试中的任何一种相比,我们提出的测试对两种方法都敏感。

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  • 作者

    Pan, Wei;

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  • 年度 2010
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  • 原文格式 PDF
  • 正文语种 en
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