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dc.contributor.authorCreswell, R
dc.contributor.authorRobinson, M
dc.contributor.authorGavaghan, D
dc.contributor.authorParag, KV
dc.contributor.authorLei, CL
dc.contributor.authorLambert, B
dc.date.accessioned2022-11-03T11:15:00Z
dc.date.issued2022-11-13
dc.date.updated2022-11-02T22:39:00Z
dc.description.abstractWhether an outbreak of infectious disease is likely to grow or dissipate is determined through the time-varying reproduction number, Rt. Real-time or retrospective identification of changes in Rt following the imposition or relaxation of interventions can thus contribute important evidence about disease transmission dynamics which can inform policymaking. Here, we present a method for estimating shifts in Rt within a renewal model framework. Our method, which we call EpiCluster, is a Bayesian nonparametric model based on the Pitman-Yor process. We assume that Rt is piecewise-constant, and the incidence data and priors determine when or whether Rt should change and how many times it should do so throughout the series. We also introduce a prior which induces sparsity over the number of changepoints. Being Bayesian, our approach yields a measure of uncertainty in Rt and its changepoints. EpiCluster is fast, straightforward to use, and we demonstrate that it provides automated detection of rapid changes in transmission, either in real-time or retrospectively, for synthetic data series where the Rt profile is known. We illustrate the practical utility of our method by fitting it to case data of outbreaks of COVID-19 in Australia and Hong Kong, where it finds changepoints coinciding with the imposition of non-pharmaceutical interventions. Bayesian nonparametric methods, such as ours, allow the volume and complexity of the data to dictate the number of parameters required to approximate the process and should find wide application in epidemiology. This manuscript was submitted as part of a theme issue on ``Modelling COVID-19 and Preparedness for Future Pandemics''.en_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.description.sponsorshipUK Foreign, Commonwealth & Development Office (FCDO)en_GB
dc.identifier.citationVol. 558, article 111351en_GB
dc.identifier.doi10.1016/j.jtbi.2022.111351
dc.identifier.grantnumberMR/R015600/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/131589
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rights© 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)en_GB
dc.subjectreproduction numberen_GB
dc.subjectBayesian nonparametricsen_GB
dc.subjectoutbreaksen_GB
dc.subjectepidemiologyen_GB
dc.subjectCOVID-19en_GB
dc.subjectchangepoint detectionen_GB
dc.titleA Bayesian nonparametric method for detecting rapid changes in disease transmissionen_GB
dc.typeArticleen_GB
dc.date.available2022-11-03T11:15:00Z
dc.identifier.issn1095-8541
dc.descriptionThis is the final version. Available on open access from Elsevier via the DOI in this recorden_GB
dc.identifier.journalJournal of Theoretical Biologyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2022-11-01
dcterms.dateSubmitted2022-07-01
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2022-11-01
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-11-02T22:39:02Z
refterms.versionFCDAM
refterms.dateFOA2022-12-02T16:21:10Z
refterms.panelBen_GB


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© 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
Except where otherwise noted, this item's licence is described as © 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)