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An efficient unified model for genome-wide association studies and genomic selection

机译:用于全基因组关联研究和基因组选择的有效统一模型

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A quantitative trait is controlled both by major variants with large genetic effects and by minor variants with small effects. Genome-wide association studies (GWAS) are an efficient approach to identify quantitative trait loci (QTL), and genomic selection (GS) with high-density single nucleotide polymorphisms (SNPs) can achieve higher accuracy of estimated breeding values than conventional best linear unbiased prediction (BLUP). GWAS and GS address different aspects of quantitative traits, but, as statistical models, they are quite similar in their description of the genetic mechanisms that underlie quantitative traits. Here, we propose a stepwise linear regression mixed model (StepLMM) to unify GWAS and GS in a single statistical model. First, the variance components of the genomic-BLUP (GBLUP) model are estimated. Then, in the SNP selection step, the linear mixed model (LMM) for GWAS is equivalently transformed into a simple linear regression to improve computation speed, and the most significant SNP is selected and included into the evaluation model. In the SNP dropping step, the SNPs in the evaluation model are tested according to the standard errors of their estimated effects. If non-significant SNPs are present, the least significant one is dropped from the model and variance components are re-estimated. We used extended Bayesian information criteria (eBIC) to evaluate the model optimization, i.e. the model with the smallest eBIC is the final one and includes only significant SNPs. We simulated scenarios with different heritabilities with 100 QTL. StepLMM estimated heritability accurately and mapped QTL precisely. Genomic prediction accuracy was much higher with StepLMM than with GBLUP. The comparison of StepLMM with other GWAS and GS methods based on a dataset from the 16th QTLMAS Workshop showed that StepLMM had medium mapping power, the lowest rate of false positives for QTL mapping, and the highest accuracy for genomic prediction. StepLMM is a combination of GWAS and GBLUP. GWAS and GBLUP are beneficial to each other in a single statistical model, GWAS improves genomic prediction accuracy, while GBLUP increases mapping precision and decreases the rate of false positives of GWAS. StepLMM has a high performance in both GWAS and GS and is feasible for agricultural breeding programs and human genetic studies.
机译:数量性状受具有较大遗传影响的主要变异和受较小遗传影响的次要变异控制。全基因组关联研究(GWAS)是一种鉴定数量性状位点(QTL)的有效方法,具有高密度单核苷酸多态性(SNP)的基因组选择(GS)可以获得比常规最佳线性无偏估计值更高的估计育种值精度预测(BLUP)。 GWAS和GS解决了数量性状的不同方面,但是作为统计模型,它们在描述构成数量性状的遗传机制方面非常相似。在这里,我们提出了一个逐步线性回归混合模型(StepLMM),以将GWAS和GS统一在一个统计模型中。首先,估计基因组BLUP(GBLUP)模型的方差分量。然后,在SNP选择步骤中,将GWAS的线性混合模型(LMM)等效转换为简单的线性回归以提高计算速度,然后选择最高有效的SNP并将其包含在评估模型中。在SNP删除步骤中,根据评估结果中的标准误差对评估模型中的SNP进行测试。如果存在不重要的SNP,则从模型中删除最不重要的SNP,并重新估计方差分量。我们使用扩展的贝叶斯信息准则(eBIC)来评估模型优化,即具有最小eBIC的模型是最终模型,并且仅包含重要的SNP。我们使用100个QTL模拟了具有不同遗传力的方案。 StepLMM可以准确地估计遗传力,并可以精确地映射QTL。 StepLMM的基因组预测精度比GBLUP高得多。根据第16届QTLMAS研讨会的数据集,对StepLMM与其他GWAS和GS方法的比较表明,StepLMM具有中等的制图能力,QTL映射的假阳性率最低,而基因组预测的准确性最高。 StepLMM是GWAS和GBLUP的组合。 GWAS和GBLUP在单一的统计模型中彼此有利,GWAS提高了基因组预测的准确性,而GBLUP提高了映射精度,并降低了GWAS的假阳性率。 StepLMM在GWAS和GS中均具有很高的性能,并且对于农业育种计划和人类遗传研究是可行的。

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