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首页> 外文期刊>Journal of Animal Science >The impact of multi-generational genotype imputation strategies on imputation accuracy and subsequent genomic predictions
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The impact of multi-generational genotype imputation strategies on imputation accuracy and subsequent genomic predictions

机译:多世代基因型拒绝策略对估算准确度和后续基因组预测的影响

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The objective of the present study was to quantify, using simulations, the impact of successive generations of genotype imputation on genomic predictions. The impact of using a small reference population of true genotypes versus a larger reference population of imputed genotypes on the accuracy of genomic predictions was also investigated. After construction of a founder population, high-density (HD) genotypes (n = 43,500 single nucleotide polymorphisms, SNP) were simulated across 25 generations (n = 46,800 per generation); a low-density genotype panel (n = 3,000 SNP) was developed from these HD genotypes, which was then used to impute genotypes using 7 alternative imputation strategies. Both low (0.03) and moderately (0.35) heritable phenotypes were simulated. Direct genomic values (DGV) were estimated using imputed genotypes from the investigated scenarios and the accuracy of predicting the simulated true breeding values (TBV) were expressed relative to the accuracy when the true genotypes were used. Mean allele concordance rate and the rate of change in mean allele concordance per generation differed between the imputation strategies investigated. Imputation was most accurate when the true HD genotypes of sires and 50% of the dams of the generation being imputed were included in the reference population; the average allele concordance rate for this scenario across generations was 0.9707. The strongest correlation between the TBV and DGV of the last generation was when the reference population included sequentially imputed HD genotypes of all previous generations, plus the true HD genotypes of all sires of the previous generations (0.987 as efficient as when the true genotypes were used in the reference population). With a moderate heritability, the correlation between the TBV and the DGV using a small reference population of accurate genotypes were, on average, 0.07 units stronger compared to DGV generated using a larger population of imputed genotypes. When the heritability was low, the accuracy of genomic predictions benefited from a larger reference population, even if SNP were imputed. The impact on the accuracy of genomic predictions from the accumulation of imputation errors across generations indicates the need to routinely generate HD genotypes on influential animals to reduce the accumulation of imputation errors over generations.
机译:本研究的目的是使用模拟来量化,连续几代基因型归咎于基因组预测的影响。还研究了使用小参考群的影响对基因组预测准确性的较大参考群体对基因组预测的准确性的影响。在构建创始人群体后,在25代(每代N = 46,800)上模拟高密度(HD)基因型(N = 43,500个单核苷酸多态性,SNP);从这些HD基因型中开发了低密度基因型面板(n = 3,000 snP),然后使用7种替代载体策略来施加基因型。模拟低(0.03)和中等(0.35)个遗传表型。使用来自所研究的情况的避税基因型估计直接基因组值(DGV),并且在使用真正基因型的准确性时,表达了预测模拟真正育种值(TBV)的准确性。平均等位基因一致性率和每代平均等位基因协调的变化率在调查的撤销策略之间不同。当岩体的真实HD基因型和所避免的产生的50%的坝体中包括在参考人口中时,估算最准确;这一场景的平均等位基因一致性率为0.9707。最后一代的TBV和DGV之间的最强相关性是当参考种群包含所有前一代的依次避税,加上前几代的所有大型的真实高清基因型(0.987,因为使用真正的基因型时有效。在参考人口中)。通过适度的可遗传性,与使用较大的抵抗基因型产生的DGV相比,TBV和DGV之间的相关性与准确基因型的小型参考群体相比,更强。当遗传性低时,即使SNP被避阻,基因组预测的准确性也受益于较大的参考群。对几代内归解误差累积的基因组预测的影响表明需要在有影响力的动物上常规产生高清基因型,以减少几代内容估算误差的累积。

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