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A Hidden Markov Model Combining Linkage and Linkage Disequilibrium Information for Haplotype Reconstruction and Quantitative Trait Locus Fine Mapping

机译:结合连锁和连锁不平衡信息的隐马尔可夫模型,用于单倍型重建和数量性状基因座精细定位

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Faithful reconstruction of haplotypes from diploid marker data (phasing) is important for many kinds of genetic analyses, including mapping of trait loci, prediction of genomic breeding values, and identification of signatures of selection. In human genetics, phasing most often exploits population information (linkage disequilibrium), while in animal genetics the primary source of information is familial (Mendelian segregation and linkage). We herein develop and evaluate a method that simultaneously exploits both sources of information. It builds on hidden Markov models that were initially developed to exploit population information only. We demonstrate that the approach improves the accuracy of allele phasing as well as imputation of missing genotypes. Reconstructed haplotypes are assigned to hidden states that are shown to correspond to clusters of genealogically related chromosomes. We show that these cluster states can directly be used to fine map QTL. The method is computationally effective at handling large data sets based on high-density SNP panels.
机译:从二倍体标记数据(定相)忠实地重建单倍型对于许多遗传分析都很重要,包括性状基因座的作图,基因组育种值的预测以及选择标记的鉴定。在人类遗传学中,定相最常利用种群信息(连锁不平衡),而在动物遗传学中,信息的主要来源是家族性的(孟德尔分离和连锁)。我们在此开发和评估一种同时利用两种信息源的方法。它建立在隐马尔可夫模型的基础上,而隐马尔可夫模型最初是为开发人口信息而开发的。我们证明该方法提高了等位基因定相的准确性以及缺失基因型的归因。将重构的单倍型分配给隐藏状态,这些隐藏状态显示为对应于族谱相关染色体的簇。我们证明了这些簇状态可以直接用于精细映射QTL。该方法在处理基于高密度SNP面板的大型数据集方面在计算上是有效的。

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