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Comparison of parametric, semiparametric and nonparametric methods in genomic evaluation

机译:基因组评估中参数,半甲酰均和非参数方法的比较

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摘要

Access to dense panels of molecular markers has facilitated genomic selection in animal breeding. The purpose of this study was to compare the nonparametric (random forest and support vector machine), semiparametric reproducing kernel Hilbert spaces (RKHS), and parametric methods (ridge regression and Bayes A) in prediction of genomic breeding values for traits with different genetic architecture. The predictive performance of different methods was compared in different combinations of distribution of QTL effects (normal and uniform), two levels of QTL numbers (50 and 200), three levels of heritability (0.1, 0.3 and 0.5), and two levels of training set individuals (1000 and 2000). To do this, a genome containing four chromosomes each 100-cM long was simulated on which 500, 1000 and 2000 evenly spaced single-nucleotide markers were distributed. With an increase in heritability and the number of markers, all the methods showed an increase in prediction accuracy (P < 0.05). By increasing the number of QTLs from 50 to 200, we found a significant decrease in the prediction accuracy of breeding value in all methods (P < 0.05). Also, with the increase in the number of training set individuals, the prediction accuracy increased significantly in all statistical methods (P < 0.05). In all the various simulation scenarios, parametric methods showed higher prediction accuracy than semiparametric and nonparametric methods. This superior mean value of prediction accuracy for parametric methods was not statistically significant compared to the semiparametric method, but it was statistically significant compared to the nonparametric method. Bayes A had the highest accuracy of prediction among all the tested methods and, is therefore, recommended for genomic evaluation.
机译:进入分子标记的致密板在动物育种中有促进基因组选择。本研究的目的是将非参数(随机森林和支持向量机)进行比较,半导体再现核Hilbert空间(RKHS)和参数方法(脊回归和贝叶斯A)预测具有不同遗传建筑的特征的基因组育种值。不同方法的预测性能在不同的QTL效应的分布组合中进行了比较(正常和均匀),QTL数量(50和200)的两个级别,遗传性三个水平(0.1,0.3和0.5),以及两种培训水平设置个人(1000和2000)。为这样做,模拟含有四种染色体的基因组,其中分布了500,1000和2000个均匀间隔的单核苷酸标记物。随着遗传性和标记数量的增加,所有方法都显示出预测准确性的增加(P <0.05)。通过增加50至200至200的QTL的数量,我们发现所有方法中繁殖值的预测精度显着降低(P <0.05)。此外,随着训练次数的增加,预测精度在所有统计方法中显着增加(P <0.05)。在所有各种仿真场景中,参数化方法显示比半甲酰胺和非参数方法更高的预测精度。与半导体方法相比,参数方法的预测精度的这种卓越的预测精度的平均值在统计学上没有显着性,但与非参数方法相比,统计学上显着。贝叶斯A在所有测试方法中具有最高的预测精度,因此建议基因组评估。

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