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      Bayesian inference of epidemiological parameters from transmission experiments

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      1 , 2 , 3 , 1 ,
      Scientific Reports
      Nature Publishing Group UK

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          Abstract

          Epidemiological parameters for livestock diseases are often inferred from transmission experiments. However, there are several limitations inherent to the design of such experiments that limits the precision of parameter estimates. In particular, infection times and latent periods cannot be directly observed and infectious periods may also be censored. We present a Bayesian framework accounting for these features directly and employ Markov chain Monte Carlo techniques to provide robust inferences and quantify the uncertainty in our estimates. We describe the transmission dynamics using a susceptible-exposed-infectious-removed compartmental model, with gamma-distributed transition times. We then fit the model to published data from transmission experiments for foot-and-mouth disease virus (FMDV) and African swine fever virus (ASFV). Where the previous analyses of these data made various assumptions on the unobserved processes in order to draw inferences, our Bayesian approach includes the unobserved infection times and latent periods and quantifies them along with all other model parameters. Drawing inferences about infection times helps identify who infected whom and can also provide insights into transmission mechanisms. Furthermore, we are able to use our models to measure the difference between the latent periods of inoculated and contact-challenged animals and to quantify the effect vaccination has on transmission.

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          Weak convergence and optimal scaling of random walk Metropolis algorithms

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            Realistic distributions of infectious periods in epidemic models: changing patterns of persistence and dynamics.

            Most mathematical models used to study the epidemiology of childhood viral diseases, such as measles, describe the period of infectiousness by an exponential distribution. The effects of including more realistic descriptions of the infectious period within SIR (susceptible/infectious/recovered) models are studied. Less dispersed distributions are seen to have two important epidemiological consequences. First, less stable behaviour is seen within the model: incidence patterns become more complex. Second, disease persistence is diminished: in models with a finite population, the minimum population size needed to allow disease persistence increases. The assumption made concerning the infectious period distribution is of a kind routinely made in the formulation of mathematical models in population biology. Since it has a major effect on the central issues of population persistence and dynamics, the results of this study have broad implications for mathematical modellers of a wide range of biological systems. Copyright 2001 Academic Press.
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              A tutorial on adaptive MCMC

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                Author and article information

                Contributors
                simon.gubbins@pirbright.ac.uk
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                1 December 2017
                1 December 2017
                2017
                : 7
                : 16774
                Affiliations
                [1 ]ISNI 0000 0004 0388 7540, GRID grid.63622.33, The Pirbright Institute, Ash Road, Pirbright, ; Surrey, GU24 0NF UK
                [2 ]ISNI 0000 0000 8809 1613, GRID grid.7372.1, Centre for Complexity Science, University of Warwick, ; Coventry, CV4 7AL UK
                [3 ]Wageningen BioVeterinary Research, Houtribweg 39, 8221 RA Lelystad, The Netherlands
                Author information
                http://orcid.org/0000-0002-7889-5380
                http://orcid.org/0000-0003-0538-4173
                Article
                17174
                10.1038/s41598-017-17174-8
                5711876
                29196741
                fd323e64-0753-46bb-b24b-3997fabe2664
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 23 May 2017
                : 21 November 2017
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