Andrianakis, Ioannis and Vernon, Ian and McCreesh, N. and McKinley, T.J. and Oakley, J.E. and Nsubuga, R. and Goldstein, M. and White, R.G. (2015) 'Bayesian history matching of complex infectious disease models using emulation : a tutorial and a case study on HIV in Uganda.', PLoS computational biology., 11 (1). e1003968.
Advances 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 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.
|Full text:||(VoR) Version of Record|
Available under License - Creative Commons Attribution.
Download PDF (1742Kb)
|Publisher Web site:||http://dx.doi.org/10.1371/journal.pcbi.1003968|
|Publisher statement:||© 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.|
|Date accepted:||08 October 2014|
|Date deposited:||03 February 2016|
|Date of first online publication:||08 January 2015|
|Date first made open access:||No date available|
Save or Share this output
|Look up in GoogleScholar|