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本文引用的文献

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BEAST: Bayesian evolutionary analysis by sampling trees.BEAST:通过抽样树进行贝叶斯进化分析。
BMC Evol Biol. 2007 Nov 8;7:214. doi: 10.1186/1471-2148-7-214.
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Tree and rate estimation by local evaluation of heterochronous nucleotide data.通过对异时核苷酸数据的局部评估进行树和速率估计。
Bioinformatics. 2007 Jan 15;23(2):169-76. doi: 10.1093/bioinformatics/btl577. Epub 2006 Nov 16.
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Relaxed phylogenetics and dating with confidence.轻松的系统发育学与可靠的年代测定。
PLoS Biol. 2006 May;4(5):e88. doi: 10.1371/journal.pbio.0040088. Epub 2006 Mar 14.
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A virus reveals population structure and recent demographic history of its carnivore host.一种病毒揭示了其食肉动物宿主的种群结构和近期种群历史。
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Large-scale sequencing of human influenza reveals the dynamic nature of viral genome evolution.对人类流感病毒的大规模测序揭示了病毒基因组进化的动态本质。
Nature. 2005 Oct 20;437(7062):1162-6. doi: 10.1038/nature04239. Epub 2005 Oct 5.
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Integrating genealogy and epidemiology: the ancestral infection and selection graph as a model for reconstructing host virus histories.整合谱系学与流行病学:以祖先感染与选择图作为重建宿主-病毒历史的模型
Theor Popul Biol. 2005 Jul;68(1):65-75. doi: 10.1016/j.tpb.2005.03.003.
7
Bayesian coalescent inference of past population dynamics from molecular sequences.基于分子序列的贝叶斯溯祖推断过去种群动态
Mol Biol Evol. 2005 May;22(5):1185-92. doi: 10.1093/molbev/msi103. Epub 2005 Feb 9.
8
Inference of demographic history from genealogical trees using reversible jump Markov chain Monte Carlo.使用可逆跳跃马尔可夫链蒙特卡罗方法从系谱树推断种群历史。
BMC Evol Biol. 2005 Jan 21;5:6. doi: 10.1186/1471-2148-5-6.
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Rise and fall of the Beringian steppe bison.白令海峡草原野牛的兴衰
Science. 2004 Nov 26;306(5701):1561-5. doi: 10.1126/science.1101074.
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Evolution of human immunodeficiency virus type 1 coreceptor usage during antiretroviral Therapy: a Bayesian approach.抗逆转录病毒治疗期间人类免疫缺陷病毒1型辅助受体使用情况的演变:一种贝叶斯方法。
J Virol. 2004 Oct;78(20):11296-302. doi: 10.1128/JVI.78.20.11296-11302.2004.

穿越崎岖天际线的平稳天空之旅:基于贝叶斯合并的种群动态推断。

Smooth skyride through a rough skyline: Bayesian coalescent-based inference of population dynamics.

作者信息

Minin Vladimir N, Bloomquist Erik W, Suchard Marc A

机构信息

Department of Statistics, University of Washington, USA.

出版信息

Mol Biol Evol. 2008 Jul;25(7):1459-71. doi: 10.1093/molbev/msn090. Epub 2008 Apr 11.

DOI:10.1093/molbev/msn090
PMID:18408232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3302198/
Abstract

Kingman's coalescent process opens the door for estimation of population genetics model parameters from molecular sequences. One paramount parameter of interest is the effective population size. Temporal variation of this quantity characterizes the demographic history of a population. Because researchers are rarely able to choose a priori a deterministic model describing effective population size dynamics for data at hand, nonparametric curve-fitting methods based on multiple change-point (MCP) models have been developed. We propose an alternative to change-point modeling that exploits Gaussian Markov random fields to achieve temporal smoothing of the effective population size in a Bayesian framework. The main advantage of our approach is that, in contrast to MCP models, the explicit temporal smoothing does not require strong prior decisions. To approximate the posterior distribution of the population dynamics, we use efficient, fast mixing Markov chain Monte Carlo algorithms designed for highly structured Gaussian models. In a simulation study, we demonstrate that the proposed temporal smoothing method, named Bayesian skyride, successfully recovers "true" population size trajectories in all simulation scenarios and competes well with the MCP approaches without evoking strong prior assumptions. We apply our Bayesian skyride method to 2 real data sets. We analyze sequences of hepatitis C virus contemporaneously sampled in Egypt, reproducing all key known aspects of the viral population dynamics. Next, we estimate the demographic histories of human influenza A hemagglutinin sequences, serially sampled throughout 3 flu seasons.

摘要

金曼合并过程为从分子序列估计群体遗传学模型参数打开了大门。一个至关重要的感兴趣参数是有效种群大小。这个数量的时间变化表征了一个种群的人口统计学历史。由于研究人员很少能够先验地选择一个确定性模型来描述手头数据的有效种群大小动态,基于多变化点(MCP)模型的非参数曲线拟合方法已经被开发出来。我们提出了一种替代变化点建模的方法,该方法利用高斯马尔可夫随机场在贝叶斯框架中实现有效种群大小的时间平滑。我们方法的主要优点是,与MCP模型相比,显式的时间平滑不需要强有力的先验决策。为了近似种群动态的后验分布,我们使用了为高度结构化高斯模型设计的高效、快速混合的马尔可夫链蒙特卡罗算法。在一项模拟研究中,我们证明了所提出的名为贝叶斯天际线的时间平滑方法在所有模拟场景中都成功地恢复了“真实”的种群大小轨迹,并且在不引入强先验假设的情况下与MCP方法竞争良好。我们将我们的贝叶斯天际线方法应用于两个真实数据集。我们分析了在埃及同时采样的丙型肝炎病毒序列,重现了病毒种群动态的所有关键已知方面。接下来,我们估计了在三个流感季节连续采样的人类甲型流感血凝素序列的人口统计学历史。