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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Fine Mapping of a Quantitative Trait Locus for Twinning Rate Using Combined Linkage and Linkage Disequilibrium Mapping
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Fine Mapping of a Quantitative Trait Locus for Twinning Rate Using Combined Linkage and Linkage Disequilibrium Mapping

机译:使用组合链接和链接不平衡映射对孪生率的定量性状基因座进行精细映射

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摘要

A novel and robust method for the fine-scale mapping of genes affecting complex traits, which combines linkage and linkage-disequilibrium information, is proposed. Linkage information refers to recombinations within the marker-genotyped generations and linkage disequilibrium to historical recombinations before genotyping started. The identity-by-descent (IBD) probabilities at the quantitative trait locus (QTL) between first generation haplotypes were obtained from the similarity of the marker alleles surrounding the QTL, whereas IBD probabilities at the QTL between later generation haplotypes were obtained by using the markers to trace the inheritance of the QTL. The variance explained by the QTL is estimated by residual maximum likelihood using the correlation structure defined by the IBD probabilities. Unlinked background genes were accounted for by fitting a polygenic variance component. The method was used to fine map a QTL for twinning rate in cattle, previously mapped on chromosome 5 by linkage analysis. The data consisted of large half-sib families, but the method could also handle more complex pedigrees. The likelihood of the putative QTL was very small along most of the chromosome, except for a sharp likelihood peak in the ninth marker bracket, which positioned the QTL within a region 1 cM in the middle part of bovine chromosome 5. The method was expected to be robust against multiple genes affecting the trait, multiple mutations at the QTL, and relatively low marker density.
机译:提出了一种新颖且鲁棒的方法,将影响复杂性状的基因进行精细标绘,该方法结合了连锁和连锁不平衡信息。连锁信息是指标记基因型分型内的重组,以及在基因分型开始前连锁不平衡与历史重组。第一代单倍型之间的数量性状基因座(QTL)的后代身份(IBD)概率是通过QTL周围的标记等位基因的相似性获得的,而第二代单倍型之间的QTL的IBD概率是通过使用标记来跟踪QTL的继承。使用IBD概率定义的相关结构,通过残差最大似然来估计QTL解释的方差。未链接的背景基因通过拟合多基因方差成分来解释。该方法用于对牛的孪生率进行QTL精细定位,该QTL先前通过连锁分析在5号染色体上定位。数据由大半同胞家庭组成,但该方法还可以处理更复杂的家谱。除第九个标记括号中的一个尖锐的似然峰将QTL定位在牛5号染色体中部<1 cM的区域外,在整个染色体的大部分中推定QTL的可能性很小。对影响性状的多个基因,QTL处的多个突变以及相对较低的标记密度具有较强的抵抗力。

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