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Multipoint Mapping of Viability and Segregation Distorting Loci Using Molecular Markers

机译:使用分子标记对生存力和偏析变异基因座进行多点定位

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In line-crossing experiments, deviations from Mendelian segregation ratios are usually observed for some markers. We hypothesize that these deviations are caused by one or more segregation-distorting loci (SDL) linked to the markers. We develop both a maximum-likelihood (ML) method and a Bayesian method to map SDL using molecular markers. The ML mapping is implemented via an EM algorithm and the Bayesian method is performed via the Markov chain Monte Carlo (MCMC). The Bayesian mapping is computationally more intensive than the ML mapping but can handle more complicated models such as multiple SDL and variable number of SDL. Both methods are applied to a set of simulated data and real data from a cross of two Scots pine trees.
机译:在交叉实验中,通常会观察到某些标记物与孟德尔偏析比的偏差。我们假设这些偏差是由一个或多个与标记相关的偏分离基因座(SDL)引起的。我们开发了最大似然(ML)方法和贝叶斯方法来使用分子标记物绘制SDL。 ML映射是通过EM算法实现的,而贝叶斯方法是通过马尔可夫链蒙特卡洛(MCMC)执行的。贝叶斯映射比ML映射在计算上更加密集,但是可以处理更复杂的模型,例如多个SDL和可变数量的SDL。两种方法都应用于来自两棵苏格兰松树的交叉的一组模拟数据和真实数据。

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