首页> 美国卫生研究院文献>other >ENABLING HIGH-THROUGHPUT GENOTYPE-PHENOTYPE ASSOCIATIONS IN THE EPIDEMIOLOGIC ARCHITECTURE FOR GENES LINKED TO ENVIRONMENT (EAGLE) PROJECT AS PART OF THE POPULATION ARCHITECTURE USING GENOMICS AND EPIDEMIOLOGY (PAGE) STUDY
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ENABLING HIGH-THROUGHPUT GENOTYPE-PHENOTYPE ASSOCIATIONS IN THE EPIDEMIOLOGIC ARCHITECTURE FOR GENES LINKED TO ENVIRONMENT (EAGLE) PROJECT AS PART OF THE POPULATION ARCHITECTURE USING GENOMICS AND EPIDEMIOLOGY (PAGE) STUDY

机译:实现高通量基因型 - 表型协会流行病学体结构的链接的人口架构环境(EaGLE)项目作为部分的基因利用基因组学和流行病学(页)研究

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摘要

Genetic association studies have rapidly become a major tool for identifying the genetic basis of common human diseases. The advent of cost-effective genotyping coupled with large collections of samples linked to clinical outcomes and quantitative traits now make it possible to systematically characterize genotype-phenotype relationships in diverse populations and extensive datasets. To capitalize on these advancements, the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project, as part of the collaborative Population Architecture using Genomics and Epidemiology (PAGE) study, accesses two collections: the National Health and Nutrition Examination Surveys (NHANES) and BioVU, Vanderbilt University’s biorepository linked to de-identified electronic medical records. We describe herein the workflows for accessing and using the epidemiologic (NHANES) and clinical (BioVU) collections, where each workflow has been customized to reflect the content and data access limitations of each respective source. We also describe the process by which these data are generated, standardized, and shared for meta-analysis among the PAGE study sites. As a specific example of the use of BioVU, we describe the data mining efforts to define cases and controls for genetic association studies of common cancers in PAGE. Collectively, the efforts described here are a generalized outline for many of the successful approaches that can be used in the era of high-throughput genotype-phenotype associations for moving biomedical discovery forward to new frontiers of data generation and analysis.
机译:遗传关联研究已迅速成为鉴定常见人类疾病遗传基础的主要工具。具有成本效益的基因分型技术的出现以及与临床结果和定量性状相关的大量样本的结合,现在使得有可能系统地表征不同人群和广泛数据集中的基因型-表型关系。为了利用这些进步,与环境有关的基因流行病学架构(EAGLE)项目是使用基因组学和流行病学(PAGE)研究的人口结构协作研究的一部分,该研究访问了两个馆藏:美国国家健康和营养调查(NHANES)和范德比尔特大学的BioVU BioVU与已取消身份识别的电子病历相关联。我们在这里描述访问和使用流行病学(NHANES)和临床(BioVU)集合的工作流程,其中每个工作流程都经过了自定义以反映每个相应来源的内容和数据访问限制。我们还将描述在PAGE研究地点之间生成,标准化和共享这些数据以进行荟萃分析的过程。作为使用BioVU的特定示例,我们描述了数据挖掘工作,以定义PAGE中常见癌症的遗传关联研究的病例和对照。总的来说,这里描述的工作是对许多成功方法的概括概述,这些方法可以在高通量基因型-表型关联时代使用,以将生物医学发现推进到数据生成和分析的新领域。

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