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A linear noise approximation for stochastic epidemic models fit to partially observed incidence counts

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  • Jonathan Fintzi
  • Jon Wakefield
  • Vladimir N. Minin

Abstract

Stochastic epidemic models (SEMs) fit to incidence data are critical to elucidating outbreak dynamics, shaping response strategies, and preparing for future epidemics. SEMs typically represent counts of individuals in discrete infection states using Markov jump processes (MJPs), but are computationally challenging as imperfect surveillance, lack of subject‐level information, and temporal coarseness of the data obscure the true epidemic. Analytic integration over the latent epidemic process is impossible, and integration via Markov chain Monte Carlo (MCMC) is cumbersome due to the dimensionality and discreteness of the latent state space. Simulation‐based computational approaches can address the intractability of the MJP likelihood, but are numerically fragile and prohibitively expensive for complex models. A linear noise approximation (LNA) that approximates the MJP transition density with a Gaussian density has been explored for analyzing prevalence data in large‐population settings, but requires modification for analyzing incidence counts without assuming that the data are normally distributed. We demonstrate how to reparameterize SEMs to appropriately analyze incidence data, and fold the LNA into a data augmentation MCMC framework that outperforms deterministic methods, statistically, and simulation‐based methods, computationally. Our framework is computationally robust when the model dynamics are complex and applies to a broad class of SEMs. We evaluate our method in simulations that reflect Ebola, influenza, and SARS‐CoV‐2 dynamics, and apply our method to national surveillance counts from the 2013–2015 West Africa Ebola outbreak.

Suggested Citation

  • Jonathan Fintzi & Jon Wakefield & Vladimir N. Minin, 2022. "A linear noise approximation for stochastic epidemic models fit to partially observed incidence counts," Biometrics, The International Biometric Society, vol. 78(4), pages 1530-1541, December.
  • Handle: RePEc:bla:biomet:v:78:y:2022:i:4:p:1530-1541
    DOI: 10.1111/biom.13538
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    References listed on IDEAS

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