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dc.contributor.authorAndrianakis, Ioannis
dc.contributor.authorVernon, Ian R.
dc.contributor.authorMcCreesh, Nicky
dc.contributor.authorMcKinley, Trevelyan J.
dc.contributor.authorOakley, Jeremy E.
dc.contributor.authorNsubuga, Rebecca N.
dc.contributor.authorGoldstein, Michael
dc.contributor.authorWhite, Richard G.
dc.date.accessioned2016-04-12T11:11:15Z
dc.date.issued2015-01
dc.description.abstractAdvances in scientific computing have allowed the development of complex models that are being routinely applied to problems in disease epidemiology, public health and decision making. The utility of these models depends in part on how well they can reproduce empirical data. However, fitting such models to real world data is greatly hindered both by large numbers of input and output parameters, and by long run times, such that many modelling studies lack a formal calibration methodology. We present a novel method that has the potential to improve the calibration of complex infectious disease models (hereafter called simulators). We present this in the form of a tutorial and a case study where we history match a dynamic, event-driven, individual-based stochastic HIV simulator, using extensive demographic, behavioural and epidemiological data available from Uganda. The tutorial describes history matching and emulation. History matching is an iterative procedure that reduces the simulator's input space by identifying and discarding areas that are unlikely to provide a good match to the empirical data. History matching relies on the computational efficiency of a Bayesian representation of the simulator, known as an emulator. Emulators mimic the simulator's behaviour, but are often several orders of magnitude faster to evaluate. In the case study, we use a 22 input simulator, fitting its 18 outputs simultaneously. After 9 iterations of history matching, a non-implausible region of the simulator input space was identified that was 10(11) times smaller than the original input space. Simulator evaluations made within this region were found to have a 65% probability of fitting all 18 outputs. History matching and emulation are useful additions to the toolbox of infectious disease modellers. Further research is required to explicitly address the stochastic nature of the simulator as well as to account for correlations between outputs.en_GB
dc.description.sponsorshipThis work was supported by a Medical Research Council (UK) grant on Model Calibration (MR/J005088/1) (http://www.mrc.ac.uk/). RGW is additionally funded by the Medical Research Council (UK) (G0802414), the Bill and Melinda Gates Foundation (TB Modelling and Analysis Consortium: Grants 21675/OPP1084276 and Consortium to Respond Effectively to the AIDS/TB Epidemic 19790.01), and CDC/PEPFAR via the Aurum Institute (U2GPS0008111). TJM is supported by Biotechnology and Biological Sciences Research Council grant number BB/I012192/1.en_GB
dc.identifier.citationVol. 11, e1003968en_GB
dc.identifier.doi10.1371/journal.pcbi.1003968
dc.identifier.otherPCOMPBIOL-D-14-00196
dc.identifier.urihttp://hdl.handle.net/10871/21067
dc.language.isoenen_GB
dc.publisherPublic Library of Scienceen_GB
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/25569850en_GB
dc.rightsCopyright: © 2015 Andrianakis et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_GB
dc.subjectAlgorithmsen_GB
dc.subjectBayes Theoremen_GB
dc.subjectComputational Biologyen_GB
dc.subjectComputer Simulationen_GB
dc.subjectFemaleen_GB
dc.subjectHIV Infectionsen_GB
dc.subjectHumansen_GB
dc.subjectMaleen_GB
dc.subjectModels, Biologicalen_GB
dc.subjectUgandaen_GB
dc.titleBayesian history matching of complex infectious disease models using emulation: a tutorial and a case study on HIV in Ugandaen_GB
dc.typeArticleen_GB
dc.date.available2016-04-12T11:11:15Z
dc.identifier.issn1553-734X
exeter.place-of-publicationUnited States
dc.descriptionPublished onlineen_GB
dc.descriptionJournal Articleen_GB
dc.descriptionResearch Support, Non-U.S. Gov'ten_GB
dc.descriptionResearch Support, U.S. Gov't, P.H.S.en_GB
dc.identifier.eissn1553-7358
dc.identifier.journalPLoS Computational Biologyen_GB


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