英国生物库:全基因组关联研究科学的光辉典范,有能力检测真实世界流行病学的复杂性。

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY
Vanessa Y Tan, Nicholas J Timpson
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引用次数: 0

摘要

全基因组关联研究(GWAS)已成功鉴定出数千个与人类性状可靠相关的基因变异。虽然全基因组关联研究仅限于某些变异频率,但它们提高了我们对复杂性状和疾病遗传结构的认识。英国生物库(UKBB)为关联研究带来了大量的分析机会和性能。纳入英国生物库数据后,许多全球基因组研究的样本量急剧扩大,从而提高了效应大小的估算能力,但关键的是,这是在表型深度和精确度使结果分析和流行病学方法的应用成为可能的情况下实现的。然而,与此同时,如此大规模、经过精心整理和深入测量的人群数据集的可用性也会增加我们面临与 GWAS 和其他分析相关的许多并发症和推论复杂性的风险。在这篇综述中,我们将讨论 UKBB 在 GWAS 时代所产生的影响、它所带来的一些机遇以及在使用这一世界领先资源的数据时所面临的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The UK Biobank: A Shining Example of Genome-Wide Association Study Science with the Power to Detect the Murky Complications of Real-World Epidemiology.

Genome-wide association studies (GWASs) have successfully identified thousands of genetic variants that are reliably associated with human traits. Although GWASs are restricted to certain variant frequencies, they have improved our understanding of the genetic architecture of complex traits and diseases. The UK Biobank (UKBB) has brought substantial analytical opportunity and performance to association studies. The dramatic expansion of many GWAS sample sizes afforded by the inclusion of UKBB data has improved the power of estimation of effect sizes but, critically, has done so in a context where phenotypic depth and precision enable outcome dissection and the application of epidemiological approaches. However, at the same time, the availability of such a large, well-curated, and deeply measured population-based collection has the capacity to increase our exposure to the many complications and inferential complexities associated with GWASs and other analyses. In this review, we discuss the impact that UKBB has had in the GWAS era, some of the opportunities that it brings, and exemplar challenges that illustrate the reality of using data from this world-leading resource.

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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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