Slade Paul F
Department of Mathematics and Statistics, Monash University, Clayton, Victoria 3168, Australia.
J Math Biol. 2002 May;44(5):427-49. doi: 10.1007/s002850100137.
It is shown how the mean ancestral times at one locus are affected in a two- locus model with recombination when information is given regarding the number of segregating sites at another locus. For samples of n genes, recursive equations are derived that describe precisely the evolution of the time-depth of such a linked genealogy. Exact numerical solutions and Markov chain Monte Carlo simulations are discussed and compared. The dependence of some properties of a singleton mutation on waiting times between events in the two-locus genealogy is quantified and illustrates the effect of recombination on these properties. The following cases are presented: (1) the distribution of the number of mutant genes in a sample arising from a singleton mutation; (2) the probability that an allele observed in a genes of a sample of size n is the ancestral type (the oldest); (3) the expectation and variance of the age of a mutant having b copies in a sample of n genes.
本文展示了在一个具有重组的双位点模型中,当给出另一个位点的分离位点数信息时,一个位点的平均祖先时间是如何受到影响的。对于n个基因的样本,推导了递归方程,这些方程精确地描述了这种连锁谱系的时间深度的演化。讨论并比较了精确数值解和马尔可夫链蒙特卡罗模拟。量化了单例突变的某些性质对双位点谱系中事件间等待时间的依赖性,并说明了重组对这些性质的影响。给出了以下几种情况:(1)由单例突变产生的样本中突变基因数目的分布;(2)在大小为n的样本的基因中观察到的一个等位基因是祖先类型(最古老的)的概率;(3)在n个基因的样本中具有b个拷贝的突变体年龄的期望和方差。