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A computationally tractable birth-death model that combines phylogenetic and epidemiological data.
Zarebski, Alexander Eugene; du Plessis, Louis; Parag, Kris Varun; Pybus, Oliver George.
Afiliación
  • Zarebski AE; Department of Zoology, University of Oxford, Oxford, United Kingdom.
  • du Plessis L; Department of Zoology, University of Oxford, Oxford, United Kingdom.
  • Parag KV; MRC Centre for Global Infectious Disease Analysis, Imperial College London, London, United Kingdom.
  • Pybus OG; Department of Zoology, University of Oxford, Oxford, United Kingdom.
PLoS Comput Biol ; 18(2): e1009805, 2022 02.
Article en En | MEDLINE | ID: mdl-35148311
ABSTRACT
Inferring the dynamics of pathogen transmission during an outbreak is an important problem in infectious disease epidemiology. In mathematical epidemiology, estimates are often informed by time series of confirmed cases, while in phylodynamics genetic sequences of the pathogen, sampled through time, are the primary data source. Each type of data provides different, and potentially complementary, insight. Recent studies have recognised that combining data sources can improve estimates of the transmission rate and the number of infected individuals. However, inference methods are typically highly specialised and field-specific and are either computationally prohibitive or require intensive simulation, limiting their real-time utility. We present a novel birth-death phylogenetic model and derive a tractable analytic approximation of its likelihood, the computational complexity of which is linear in the size of the dataset. This approach combines epidemiological and phylodynamic data to produce estimates of key parameters of transmission dynamics and the unobserved prevalence. Using simulated data, we show (a) that the approximation agrees well with existing methods, (b) validate the claim of linear complexity and (c) explore robustness to model misspecification. This approximation facilitates inference on large datasets, which is increasingly important as large genomic sequence datasets become commonplace.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Brotes de Enfermedades / Genómica Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Brotes de Enfermedades / Genómica Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido