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首页> 外文期刊>Genetics, selection, evolution >Accuracy of genotype imputation based on random and selected reference sets in purebred and crossbred sheep populations and its effect on accuracy of genomic prediction
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Accuracy of genotype imputation based on random and selected reference sets in purebred and crossbred sheep populations and its effect on accuracy of genomic prediction

机译:基于纯种和杂种绵羊种群的随机和选择参考集的基因型推算准确性及其对基因组预测准确性的影响

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The objectives of this study were to investigate the accuracy of genotype imputation from low (12k) to medium (50k Illumina-Ovine) SNP (single nucleotide polymorphism) densities in purebred and crossbred Merino sheep based on a random or selected reference set and to evaluate the impact of using imputed genotypes on accuracy of genomic prediction. Imputation validation sets were composed of random purebred or crossbred Merinos, while imputation reference sets were of variable sizes and included random purebred or crossbred Merinos or a group of animals that were selected based on high genetic relatedness to animals in the validation set. The Beagle software program was used for imputation and accuracy of imputation was assessed based on the Pearson correlation coefficient between observed and imputed genotypes. Genomic evaluation was performed based on genomic best linear unbiased prediction and its accuracy was evaluated as the Pearson correlation coefficient between genomic estimated breeding values using either observed (12k/50k) or imputed genotypes with varying levels of imputation accuracy and accurate estimated breeding values based on progeny-tests. Imputation accuracy increased as the size of the reference set increased. However, accuracy was higher for purebred Merinos that were imputed from other purebred Merinos (on average 0.90 to 0.95 based on 1000 to 3000 animals) than from crossbred Merinos (0.78 to 0.87 based on 1000 to 3000 animals) or from non-Merino purebreds (on average 0.50). The imputation accuracy for crossbred Merinos based on 1000 to 3000 other crossbred Merino ranged from 0.86 to 0.88. Considerably higher imputation accuracy was observed when a selected reference set with a high genetic relationship to target animals was used vs. a random reference set of the same size (0.96 vs. 0.88, respectively). Accuracy of genomic prediction based on 50k genotypes imputed with high accuracy (0.88 to 0.99) decreased only slightly (0.0 to 0.67 % across traits) compared to using observed 50k genotypes. Accuracy of genomic prediction based on observed 12k genotypes was higher than accuracy based on lowly accurate (0.62 to 0.86) imputed 50k genotypes.
机译:这项研究的目的是基于随机或选择的参考集,研究纯种和杂交美利奴羊中低(12k)至中等(50k Illumina-Ovine)SNP(单核苷酸多态性)密度基因型估算的准确性,并进行评估使用估算基因型对基因组预测准确性的影响。归因验证集由随机的纯种或杂交美利奴羊组成,而归因参考集具有可变的大小,包括随机的纯种或杂交美利奴羊或一组基于与验证集中与动物高度遗传相关性而选择的动物。使用Beagle软件程序进行估算,并根据观察到的和估算的基因型之间的皮尔森相关系数评估估算的准确性。基因组评估是基于最佳的基因组线性无偏预测进行的,其准确性被评估为使用观察值(12k / 50k)或估算基因型的基因组估计育种值之间的皮尔森相关系数,而估算基因型的准确度各不相同,并且基于后代测试。归因精度随参考集大小的增加而增加。但是,从其他纯种美利奴羊(基于1000至3000只动物的平均0.90至0.95)推算出的纯种美利奴人,其准确度要高于杂交美利奴羊(基于1000至3000只动物的0.78至0.87)或非美利奴纯种(平均0.50)。基于1000至3000个其他杂交美利奴羊的杂交美利奴羊的插补准确度为0.86至0.88。当使用与目标动物具有高度遗传关系的选定参考集相对于相同大小的随机参考集(分别为0.96和0.88)时,观察到的插补准确度要高得多。与使用观察到的50k基因型相比,基于高精度估算的50k基因型的基因组预测准确性(0.88至0.99)仅略微降低(整个性状的0.0%至0.67%)。基于观察到的12k基因型的基因组预测准确性高于基于低准确度(0.62至0.86)推算的50k基因型的准确性。

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