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Statistical power for identifying nucleotide markers associated with quantitative traits in genome-wide association analysis using a mixed model

机译:使用混合模型在全基因组关联分析中鉴定与定量性状相关的核苷酸标记的统计能力

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摘要

Use of mixed models is in the spotlight as an emerging method for genome-wide association studies (GWASs). This study investigated the statistical power for identifying nucleotide variants associated with quantitative traits using the mixed model methodology. Quantitative traits were simulated through design of heritability, the number of causal variants (NCV), the number of polygenic variants, and genetic variance ratio of causal to polygenic variants (VRCTP). Statistical power estimates were influenced not only by individual factors of heritability, NCV, and VRCTP, but also by their interactions (P < 0.05). As the genetic variance ratio decreased, the difference in power between heritabilities of 0.3 and 0.5 increased with the use of 20 causal variants, but decreased when there were 100 causal variants (P < 0.05). The power empirically estimated from the simulation study would be applicable to the design of GWAS for quantitative traits with known genetic parameters by predicting the degree of false negative associations. (C) 2014 Elsevier Inc. All rights reserved.
机译:混合模型的使用已成为关注全基因组关联研究(GWAS)的新兴方法。这项研究调查了使用混合模型方法鉴定与定量性状相关的核苷酸变异的统计能力。通过设计遗传力,因果变异数(NCV),多基因变异数和因果与多基因变异的遗传变异比(VRCTP)设计模拟数量性状。统计功效估计不仅受遗传力,NCV和VRCTP的各个因素影响,还受到它们之间的相互作用的影响(P <0.05)。随着遗传方差比率的降低,使用20个因果变异体时,遗传力0.3和0.5之间的功效差异增加,而当存在100个因果变异体时,遗传力之间的功效差异减小(P <0.05)。从模拟研究中凭经验估算的功率将可用于通过预测假阴性关联程度来设计具有已知遗传参数的数量性状的GWAS。 (C)2014 Elsevier Inc.保留所有权利。

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