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Using public control genotype data to increase power and decrease cost of case-control genetic association studies.

机译:使用公共控制基因型数据来增加病例对照遗传协会研究的能力并降低成本。

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摘要

Genome-wide association (GWA) studies are a powerful approach for identifying novel genetic risk factors associated with human disease. A GWA study typically requires the inclusion of thousands of samples to have sufficient statistical power to detect single nucleotide polymorphisms that are associated with only modest increases in risk of disease given the heavy burden of a multiple test correction that is necessary to maintain valid statistical tests. Low statistical power and the high financial cost of performing a GWA study remains prohibitive for many scientific investigators anxious to perform such a study using their own samples. A number of remedies have been suggested to increase statistical power and decrease cost, including the utilization of free publicly available genotype data and multi-stage genotyping designs. Herein, we compare the statistical power and relative costs of alternative association study designs that use cases and screened controls to study designs that are based only on, or additionally include, free public control genotype data. We describe a novel replication-based two-stage study design, which uses free public control genotype data in the first stage and follow-up genotype data on case-matched controls in the second stage that preserves many of the advantages inherent when using only an epidemiologically matched set of controls. Specifically, we show that our proposed two-stage design can substantially increase statistical power and decrease cost of performing a GWA study while controlling the type-I error rate that can be inflated when using public controls due to differences in ancestry and batch genotype effects.
机译:全基因组协会(GWA)研究是一种确定与人类疾病相关的新型遗传风险因素的有效方法。 GWA研究通常要求包括成千上万的样本,以具有足够的统计能力来检测单核苷酸多态性,而鉴于维持有效统计测试所必需的多重测试校正的沉重负担,这种单核苷酸多态性仅与疾病风险的适度增加相关。进行GWA研究的低统计能力和高昂的财务成本对于许多急于使用自己的样本进行此类研究的科研人员而言仍然是令人望而却步的。已经提出了许多方法来增加统计能力并降低成本,包括利用免费的公共可用基因型数据和多阶段基因分型设计。在本文中,我们比较了使用案例和筛选后的对照的替代关联研究设计的统计功效和相对成本,以研究仅基于或另外包括免费公共对照基因型数据的设计。我们描述了一种新颖的基于复制的两阶段研究设计,该研究设计在第一阶段使用免费的公共对照基因型数据,在第二阶段使用病例匹配对照的后续基因型数据,从而保留了仅使用流行病学匹配的控件集。具体而言,我们表明,我们提出的两阶段设计可以大大提高统计能力并降低进行GWA研究的成本,同时控制由于祖先和批次基因型效应的差异而在使用公共控件时可能夸大的I型错误率。

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