首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Genomewide Rapid Association Using Mixed Model and Regression: A Fast and Simple Method For Genomewide Pedigree-Based Quantitative Trait Loci Association Analysis
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Genomewide Rapid Association Using Mixed Model and Regression: A Fast and Simple Method For Genomewide Pedigree-Based Quantitative Trait Loci Association Analysis

机译:全基因组快速关联使用混合模型和回归:基于基因组谱系的定量性状位点关联分析的快速简便方法

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For pedigree-based quantitative trait loci (QTL) association analysis, a range of methods utilizing within-family variation such as transmission-disequilibrium test (TDT)-based methods have been developed. In scenarios where stratification is not a concern, methods exploiting between-family variation in addition to within-family variation, such as the measured genotype (MG) approach, have greater power. Application of MG methods can be computationally demanding (especially for large pedigrees), making genomewide scans practically infeasible. Here we suggest a novel approach for genomewide pedigree-based quantitative trait loci (QTL) association analysis: genomewide rapid association using mixed model and regression (GRAMMAR). The method first obtains residuals adjusted for family effects and subsequently analyzes the association between these residuals and genetic polymorphisms using rapid least-squares methods. At the final step, the selected polymorphisms may be followed up with the full measured genotype (MG) analysis. In a simulation study, we compared type 1 error, power, and operational characteristics of the proposed method with those of MG and TDT-based approaches. For moderately heritable (30%) traits in human pedigrees the power of the GRAMMAR and the MG approaches is similar and is much higher than that of TDT-based approaches. When using tabulated thresholds, the proposed method is less powerful than MG for very high heritabilities and pedigrees including large sibships like those observed in livestock pedigrees. However, there is little or no difference in empirical power of MG and the proposed method. In any scenario, GRAMMAR is much faster than MG and enables rapid analysis of hundreds of thousands of markers.
机译:对于基于谱系的数量性状基因座(QTL)关联分析,已经开发了一系列利用家庭内部变异的方法,例如基于传输不平衡检验(TDT)的方法。在不关心分层的情况下,除了家庭内部变异之外,利用家庭之间变异的方法(例如测得的基因型(MG)方法)具有更大的优势。 MG方法的应用可能在计算上要求很高(特别是对于较大的谱系),这使得全基因组扫描实际上不可行。在这里,我们建议基于谱系的定量性状基因座(QTL)关联分析的一种新方法:使用混合模型和回归(GRAMMAR)的全基因组快速关联。该方法首先获得针对家庭效应调整的残基,然后使用快速最小二乘法分析这些残基与遗传多态性之间的关联。在最后一步,可以对所选的多态性进行完整的基因型(MG)分析。在仿真研究中,我们比较了该方法与基于MG和TDT的方法的类型1的误差,功率和操作特性。对于人类谱系中度可遗传(30%)的特征,GRAMMAR和MG方法的功能相似,并且比基于TDT的方法高得多。当使用列表阈值时,对于很高的遗传力和谱系,包括像牲畜谱系中观察到的大同胞,所提出的方法不如MG强大。但是,MG的经验能力与所提出的方法几乎没有差异。在任何情况下,GRAMMAR都比MG快得多,并且可以快速分析成千上万个标记。

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