Evidence map›Paper›PMID 41042801›Full record

ArticlePLoS computational biology2025

A Bayesian model for repeated cross-sectional epidemic prevalence survey data.

Nicholas Steyn, Marc Chadeau-Hyam, Paul Elliott, Christl A Donnelly

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Nicholas SteynDepartment of Statistics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-8904-2941
Marc Chadeau-HyamMRC Centre for Environment and Health, School of Public Health, Imperial College London, London, United Kingdom.
Paul ElliottMRC Centre for Environment and Health, School of Public Health, Imperial College London, London, United Kingdom.ORCID 0000-0002-7511-5684
Christl A DonnellyDepartment of Statistics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-0195-2463

Funding

Cancer Research UK 22184H2020-EXPANSEMedical Research Council MR/L01341X/1Medical Research Council MR/S019669/1Medical Research Council MR/V030841/1NIHR Health Protection Research Unit in Emerging and Zoonotic InfectionsOxford Martin Programme in Digital Pandemic PreparednessVaccine Efficacy Evaluation for Priority Emerging Diseases
6 · The paper itself

Abstract

Epidemic prevalence surveys monitor the spread of an infectious disease by regularly testing representative samples of a population for infection. State-of-the-art Bayesian approaches for analysing epidemic survey data were constructed independently and under pressure during the COVID-19 pandemic. In this paper, we compare two existing approaches (one leveraging Bayesian P-splines and the other approximate Gaussian processes) with a novel approach (leveraging a random walk and fit using sequential Monte Carlo) for smoothing and performing inference on epidemic survey data. We use our simpler approach to investigate the impact of survey design and underlying epidemic dynamics on the quality of estimates. We then incorporate these considerations into the existing approaches and compare all three on simulated data and on real-world data from the SARS-CoV-2 REACT-1 prevalence study in England. All three approaches, once appropriate considerations are made, produce similar estimates of infection prevalence; however, estimates of the growth rate and instantaneous reproduction number are more sensitive to underlying assumptions. Interactive notebooks applying all three approaches are also provided alongside recommendations on hyperparameter selection and other practical guidance, with some cases resulting in orders-of-magnitude faster runtime.

Indexed as

EpidemicsEpidemiological MonitoringBayes TheoremComputational BiologyComputer SimulationCOVID-19Cross-Sectional StudiesEnglandEpidemiologyHumansModels, StatisticalPandemicsPrevalenceSARS-CoV-2

Identifiers

PMID41042801
PMCPMC12507252

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.