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LPG: A four-group probabilistic approach to leveraging pleiotropy in genome-wide association studies

机译:LPG:在全基因组关联研究中利用多效性的四组概率方法

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摘要

BackgroundTo date, genome-wide association studies (GWAS) have successfully identified tens of thousands of genetic variants among a variety of traits/diseases, shedding light on the genetic architecture of complex disease. The polygenicity of complex diseases is a widely accepted phenomenon through which a vast number of risk variants, each with a modest individual effect, collectively contribute to the heritability of complex diseases. This imposes a major challenge on fully characterizing the genetic bases of complex diseases. An immediate implication of polygenicity is that a much larger sample size is required to detect individual risk variants with weak/moderate effects. Meanwhile, accumulating evidence suggests that different complex diseases can share genetic risk variants, a phenomenon known as pleiotropy.
机译:背景技术迄今为止,全基因组关联研究(GWAS)已成功鉴定出各种性状/疾病中成千上万的遗传变异,为复杂疾病的遗传结构提供了亮点。复杂疾病的多基因性是一种广为接受的现象,通过该现象,各种风险变体(各自具有适度的个体效应)共同促进了复杂疾病的遗传性。这对全面表征复杂疾病的遗传基础提出了重大挑战。多基因性的直接含义是,需要更大的样本量来检测具有弱/中度影响的个体风险变体。同时,越来越多的证据表明,不同的复杂疾病可以共享遗传风险变异,这种现象被称为多效性。

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