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Use of meta-analyses and joint analyses to select variants in whole genome sequences for genomic evaluation: An application in milk production of French dairy cattle breeds

机译:使用荟萃分析和联合分析在全基因组序列中选择变异体进行基因组评估:法国奶牛品种在牛奶生产中的应用

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ABSTRACTAs a result of the 1000 Bull Genome Project, it has become possible to impute millions of variants, with many of these potentially causative for traits of interest, for thousands of animals that have been genotyped with medium-density chips. This enormous source of data opens up very interesting possibilities for the inclusion of these variants in genomic evaluations. However, for computational reasons, it is not possible to include all variants in genomic evaluation procedures. One potential approach could be to select the most relevant variants based on the results of genome-wide association studies (GWAS); however, the identification of causative mutations is still difficult with this method, partly because of weak imputation accuracy for rare variants. To address this problem, this study assesses the ability of different approaches based on multi-breed GWAS (joint and meta-analyses) to identify single-nucleotide polymorphisms (SNP) for use in genomic evaluation in the 3 main French dairy cattle breeds. A total of 6,262 Holstein bulls, 2,434 Montbéliarde bulls, and 2,175 Normande bulls with daughter yield deviations for 5 milk production traits were imputed for 27 million variants. Within-breed and joint (including all 3 breeds) GWAS were performed and 3 models of meta-analysis were tested: fixed effect, random effect, and Z-score. Comparison of the results of within- and multi-breed GWAS showed that most of the quantitative trait loci identified using within-breed approaches were also found with multi-breed methods. However, the most significant variants identified in each region differed depending on the method used. To determine which approach highlighted the most predictive SNP for each trait, we used a marker-assisted best unbiased linear prediction model to evaluate lists of SNP generated by the different GWAS methods; each list contained between 25 and 2,000 candidate variants per trait, which were identified using a single within- or multi-breed GWAS approach. Among all the multi-breed methods tested in this study, variant selection based on meta-analysis (fixed effect) resulted in the most-accurate genomic evaluation (+1 to +3 points compared with other multi-breed approaches). However, the accuracies of genomic evaluation were always better when variants were selected using the results of within-breed GWAS. As has generally been found in studies of quantitative trait loci, these results suggest that part of the genetic variance of milk production traits is breed specific in Holstein, Montbéliarde, and Normande cattle.
机译:ABSTRACTA是“ 1000 Bull基因组计划”的结果,对于成千上万用中密度芯片进行基因分型的动物来说,已经有可能推算出数百万个变体,其中许多潜在地引起了所关注的性状。巨大的数据来源为将这些变异体纳入基因组评估开辟了非常有趣的可能性。但是,由于计算上的原因,不可能在基因组评估程序中包括所有变体。一种可能的方法是根据全基因组关联研究(GWAS)的结果选择最相关的变体。然而,用这种方法鉴定致病突变仍然很困难,部分原因是稀有变异的估算准确性较弱。为了解决这个问题,本研究评估了基于多品种GWAS(联合分析和荟萃分析)的不同方法鉴定单核苷酸多态性(SNP)以用于法国3个主要奶牛品种的基因组评估的能力。估算了5种奶牛生产性状的6 262头荷斯坦公牛,2 434头蒙贝利亚德公牛和2 175头诺曼德公牛的子代产量差异,估算了2700万个变种。进行了品种内和联合(包括所有3个品种)的GWAS,并测试了3种荟萃分析模型:固定效应,随机效应和Z评分。对内部和全品种GWAS结果的比较表明,使用内部品种方法鉴定的大多数数量性状基因座也可以通过多种品种方法找到。但是,根据使用的方法,在每个区域中识别出的最重要的变体有所不同。为了确定哪种方法突出了每个性状的最可预测的SNP,我们使用了标记辅助的最佳无偏线性预测模型来评估由不同GWAS方法生成的SNP列表。每个列表包含每个性状25至2,000个候选变体,这些变体使用单一的内部或多品种GWAS方法进行鉴定。在这项研究中测试的所有多品种方法中,基于荟萃分析(固定效应)的变体选择导致了最准确的基因组评估(与其他多品种方法相比,得分为+1至+3分)。但是,使用内部GWAS的结果选择变体时,基因组评估的准确性始终更好。正如在数量性状基因座研究中通常发现的那样,这些结果表明,奶牛生产性状的部分遗传变异在霍尔斯坦,蒙贝利亚德和诺曼德牛中是特定品种的。

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