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本文引用的文献

1
Mitochondrial DNA and human evolution.线粒体DNA与人类进化。
Annu Rev Genomics Hum Genet. 2005;6:165-83. doi: 10.1146/annurev.genom.6.080604.162249.
2
Estimation of effective population sizes from data on genetic markers.根据遗传标记数据估算有效种群大小。
Philos Trans R Soc Lond B Biol Sci. 2005 Jul 29;360(1459):1395-409. doi: 10.1098/rstb.2005.1682.
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Understanding differences between phylogenetic and pedigree-derived mtDNA mutation rate: a model using families from the Azores Islands (Portugal).了解系统发育和家系衍生的线粒体DNA突变率之间的差异:一项使用来自亚速尔群岛(葡萄牙)家庭的模型研究
Mol Biol Evol. 2005 Jun;22(6):1490-505. doi: 10.1093/molbev/msi141. Epub 2005 Apr 6.
4
Bayesian analysis of an admixture model with mutations and arbitrarily linked markers.具有突变和任意连锁标记的混合模型的贝叶斯分析。
Genetics. 2005 Mar;169(3):1727-38. doi: 10.1534/genetics.104.036236. Epub 2005 Jan 16.
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Genetic evidence supports demic diffusion of Han culture.遗传学证据支持汉文化的人口扩散。
Nature. 2004 Sep 16;431(7006):302-5. doi: 10.1038/nature02878.
6
Estimating admixture proportions with microsatellites: comparison of methods based on simulated data.利用微卫星估计混合比例:基于模拟数据的方法比较
Mol Ecol. 2004 Apr;13(4):955-68. doi: 10.1111/j.1365-294x.2004.02107.x.
7
Markov chain Monte Carlo without likelihoods.无似然马尔可夫链蒙特卡罗方法。
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8
METHODS OF ANALYSIS OF THE GENETIC COMPOSITION OF A HYBRID POPULATION.杂交群体遗传组成的分析方法
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9
The dynamics of racial intermixture; an analysis based on the American Negro.种族混合的动态变化;基于美国黑人的分析
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10
Three novel mtDNA restriction site polymorphisms allow exploration of population affinities of African Americans.三种新的线粒体DNA限制性位点多态性有助于探究非裔美国人的群体亲缘关系。
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一种基于溯祖理论的DNA序列混合估计方法。

A coalescent-based estimator of admixture from DNA sequences.

作者信息

Wang Jinliang

机构信息

Institute of Zoology, Zoological Society of London, London NW1 4RY, United Kingdom.

出版信息

Genetics. 2006 Jul;173(3):1679-92. doi: 10.1534/genetics.105.054130. Epub 2006 Apr 19.

DOI:10.1534/genetics.105.054130
PMID:16624918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1526692/
Abstract

A variety of estimators have been developed to use genetic marker information in inferring the admixture proportions (parental contributions) of a hybrid population. The majority of these estimators used allele frequency data, ignored molecular information that is available in markers such as microsatellites and DNA sequences, and assumed that mutations are absent since the admixture event. As a result, these estimators may fail to deliver an estimate or give rather poor estimates when admixture is ancient and thus mutations are not negligible. A previous molecular estimator based its inference of admixture proportions on the average coalescent times between pairs of genes taken from within and between populations. In this article I propose an estimator that considers the entire genealogy of all of the sampled genes and infers admixture proportions from the numbers of segregating sites in DNA sequence samples. By considering the genealogy of all sequences rather than pairs of sequences, this new estimator also allows the joint estimation of other interesting parameters in the admixture model, such as admixture time, divergence time, population size, and mutation rate. Comparative analyses of simulated data indicate that the new coalescent estimator generally yields better estimates of admixture proportions than the previous molecular estimator, especially when the parental populations are not highly differentiated. It also gives reasonably accurate estimates of other admixture parameters. A human mtDNA sequence data set was analyzed to demonstrate the method, and the analysis results are discussed and compared with those from previous studies.

摘要

已经开发出多种估计方法,用于利用遗传标记信息推断杂交群体的混合比例(亲本贡献)。这些估计方法大多使用等位基因频率数据,忽略了微卫星和DNA序列等标记中可用的分子信息,并假设自混合事件以来不存在突变。因此,当混合事件发生时间久远且突变不可忽略时,这些估计方法可能无法给出估计值,或者给出的估计值相当不准确。之前的一种分子估计方法是基于从群体内部和群体之间选取的基因对之间的平均合并时间来推断混合比例。在本文中,我提出了一种估计方法,该方法考虑所有采样基因的完整谱系,并根据DNA序列样本中的分离位点数量推断混合比例。通过考虑所有序列的谱系而非序列对,这种新的估计方法还允许对混合模型中的其他有趣参数进行联合估计,例如混合时间、分化时间、群体大小和突变率。对模拟数据的比较分析表明,新的合并估计方法通常比之前的分子估计方法能更好地估计混合比例,尤其是当亲本群体差异不大时。它还能对其他混合参数给出合理准确的估计。对一个人类线粒体DNA序列数据集进行了分析以演示该方法,并对分析结果进行了讨论,并与之前研究的结果进行了比较。