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Infectious Disease Dynamics Inferred from Genetic Data via Sequential MonteCarlo

机译:从遗传数据通过顺序Monte推断出的传染病动态卡洛

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摘要

Genetic sequences from pathogens can provide information about infectious disease dynamics that may supplement or replace information from other epidemiological observations. Most currently available methods first estimate phylogenetic trees from sequence data, then estimate a transmission model conditional on these phylogenies. Outside limited classes of models, existing methods are unable to enforce logical consistency between the model of transmission and that underlying the phylogenetic reconstruction. Such conflicts in assumptions can lead to bias in the resulting inferences. Here, we develop a general, statistically efficient, plug-and-play method to jointly estimate both disease transmission and phylogeny using genetic data and, if desired, other epidemiological observations. This method explicitly connects the model of transmission and the model of phylogeny so as to avoid the aforementioned inconsistency. We demonstrate the feasibility of our approach through simulation and apply it to estimate stage-specific infectiousness in a subepidemic of human immunodeficiency virus in Detroit, Michigan. In a supplement, we prove that our approach is a valid sequential Monte Carlo algorithm. While we focus on how these methods may be applied to population-level models of infectious disease, their scope is more general. These methods may be applied in other biological systems where one seeks to infer population dynamics from genetic sequences,and they may also find application for evolutionary models with phenotypic rather thangenotypic data.
机译:来自病原体的遗传序列可以提供有关传染病动态的信息,可以补充或替代来自其他流行病学观察的信息。最当前可用的方法首先从序列数据估计系统发育树,然后估计以这些系统发育为条件的传播模型。在有限的模型类别之外,现有方法无法在传播模型与系统发育重建基础之间实现逻辑一致性。假设中的此类冲突可能导致结果推论产生偏差。在这里,我们开发了一种通用的,统计有效的即插即用方法,可以使用遗传数据和其他流行病学观察(如果需要)共同估算疾病传播和系统发育。该方法明确地将传播模型和系统发育模型连接起来,以避免上述不一致。我们通过仿真演示了我们方法的可行性,并将其应用于在密歇根州底特律的人类免疫缺陷病毒亚流行中评估特定阶段的传染性。作为补充,我们证明我们的方法是有效的顺序蒙特卡洛算法。尽管我们重点关注这些方法如何应用于人群水平的传染病模型,但它们的范围更为广泛。这些方法可能会应用于其他试图从遗传序列推断种群动态的生物系统中,他们可能还会发现具有表型而不是表型的进化模型的应用基因型数据。

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