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无限等位基因模型下无选择时连锁不平衡的抽样分布。

The sampling distribution of linkage disequilibrium under an infinite allele model without selection.

作者信息

Hudson R R

出版信息

Genetics. 1985 Mar;109(3):611-31. doi: 10.1093/genetics/109.3.611.

Abstract

The sampling distributions of several statistics that measure the association of alleles on gametes (linkage disequilibrium) are estimated under a two-locus neutral infinite allele model using an efficient Monte Carlo method. An often used approximation for the mean squared linkage disequilibrium is shown to be inaccurate unless the proper statistical conditioning is used. The joint distribution of linkage disequilibrium and the allele frequencies in the sample is studied. This estimated joint distribution is sufficient for obtaining an approximate maximum likelihood estimate of C = 4Nc, where N is the population size and c is the recombination rate. It has been suggested that observations of high linkage disequilibrium might be a good basis for rejecting a neutral model in favor of a model in which natural selection maintains genetic variation. It is found that a single sample of chromosomes, examined at two loci cannot provide sufficient information for such a test if C less than 10, because with C this small, very high levels of linkage disequilibrium are not unexpected under the neutral model. In samples of size 50, it is found that, even when C is as large as 50, the distribution of linkage disequilibrium conditional on the allele frequencies is substantially different from the distribution when there is no linkage between the loci. When conditioned on the number of alleles at each locus in the sample, all of the sample statistics examined are nearly independent of theta = 4N mu, where mu is the neutral mutation rate.

摘要

使用一种有效的蒙特卡罗方法,在双位点中性无限等位基因模型下估计了几种测量配子上等位基因关联(连锁不平衡)的统计量的抽样分布。结果表明,除非使用适当的统计条件,否则常用的平均平方连锁不平衡近似值是不准确的。研究了连锁不平衡与样本中等位基因频率的联合分布。这种估计的联合分布足以获得C = 4Nc的近似最大似然估计值,其中N是种群大小,c是重组率。有人提出,高连锁不平衡的观察结果可能是拒绝中性模型而支持自然选择维持遗传变异模型的良好依据。研究发现,如果C小于10,那么在两个位点上检查的单个染色体样本不能为这样的检验提供足够的信息,因为在中性模型下,当C如此之小时,非常高的连锁不平衡水平并不意外。在大小为50的样本中,研究发现,即使C高达50,基于等位基因频率的连锁不平衡分布与位点之间无连锁时的分布也有很大不同。当基于样本中每个位点的等位基因数量进行条件设定时,所检查的所有样本统计量几乎都与θ = 4Nμ无关,其中μ是中性突变率。

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