利用基因组广泛选择和高密度SNP筛选预测奶牛乳腺炎和生育力的遗传优势。

H W Raadsma, G Moser, R E Crump, M S Khatkar, K R Zenger, J A L Cavanagh, R J Hawken, M Hobbs, W Barris, J Solkner, F W Nicholas, B Tier
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引用次数: 14

摘要

研究了两种新的全基因组选择(GWS)方法,用于仅利用SNP信息预测动物的遗传优点。对1546头具有可靠ebv的奶牛进行了基因分型,对跨越整个牛基因组的15380个snp进行了分型。利用偏最小二乘法(PLS)和遗传算法回归(GAR)两种复杂性降低方法,根据SNP信息找到ebv的最优解。广泛的内部交叉验证用于寻找最佳预测模型,然后进行外部验证(不直接使用谱系或SNP位置)。PLS和GAR均能准确拟合体细胞计数(SCC)(最大r = 0.83)和生育力(最大r = 0.88)的训练数据集,SCC和生育力的预测精度分别为r = 0.47和r = 0.72。这是第一个实证证明,基因组广泛选择可以解释非常高比例的适应性性状的加性遗传变异,同时只利用一小部分可用的SNP信息,而不使用系谱或QTL定位。PLS的计算效率高于GAR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting genetic merit for mastitis and fertility in dairy cattle using genome wide selection and high density SNP screens.

Two novel methods for genome wide selection (GWS) were examined for predicting the genetic merit of animals using SNP information alone. A panel of 1,546 dairy bulls with reliable EBVs was genotyped for 15,380 SNPs that spanned the whole bovine genome. Two complexity reduction methods were used, partial least squares (PLS) and regression using a genetic algorithm (GAR), to find optimal solutions of EBVs against SNP information. Extensive internal cross-validation was used tofind the best predictive models followed by external validation (without direct use of the pedigree or SNP location). Both PLS and GAR provided both accurate fit to the training data set for somatic cell count (SCC) (max r = 0.83) and fertility (max r = 0.88) and showed an accuracy of prediction of r = 0.47 for SCC, and r = 0.72 for fertility. This is the first empirical demonstration that genome wide selection can account for a very high proportion of additive genetic variation in fitness traits whilst exploiting only a small percentage of available SNP information, without use of pedigree or QTL mapping. PLS was computationally more efficient than GAR.

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