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Bayesian model selection for multiple QTLs mapping combining linkage disequilibrium and linkage

机译:结合连锁不平衡和连锁的多个QTL映射的贝叶斯模型选择

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Linkage disequilibrium (LD) mapping is able to localize quantitative trait loci (QTL) within a rather small region (e.g. 2 cM), which is much narrower than linkage analysis (LA, usually 20 cM). The multilocus LD method utilizes haplotype information around putative mutation and takes historical recombination events into account, and thus provides a powerful method for further fine mapping. However, sometimes there are more than one QTLs in the region being studied. In this study, the Bayesian model selection implemented via the Markov chain Monte Carlo (MCMC) method is developed for fine mapping of multiple QTLs using haplotype information in a small region. The method combines LD as well as linkage information. A series of simulation experiments were conducted to investigate the behavior of the method. The results showed that this new multiple QTLs method was more efficient in separating closely linked QTLs than single-marker association studies.
机译:连锁不平衡(LD)映射能够在相当小的区域(例如2 cM)内定位定量性状基因座(QTL),该区域比连锁分析(LA,通常为20 cM)窄得多。多基因座LD方法利用推定突变周围的单倍型信息,并考虑到历史重组事件,从而为进一步精细定位提供了有力的方法。但是,有时正在研究的区域中存在多个QTL。在这项研究中,开发了通过马尔可夫链蒙特卡洛(MCMC)方法实现的贝叶斯模型选择,以便在一个小区域内使用单倍型信息精细映射多个QTL。该方法结合了LD以及链接信息。进行了一系列模拟实验以研究该方法的行为。结果表明,这种新的多重QTL方法比单标记关联研究在分离紧密联系的QTL方面更有效。

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