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Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models
Earlier research has suggested that approximate Bayesian computation (ABC) makes it possible to fit simulator-based intractable birth–death models to investigate communicable disease outbreak dynamics with accuracy comparable to that of exact Bayesian methods. However, recent findings have indicated...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514576/ https://www.ncbi.nlm.nih.gov/pubmed/37744419 http://dx.doi.org/10.12688/wellcomeopenres.15048.2 |
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author | Lintusaari, Jarno Blomstedt, Paul Rose, Brittany Sivula, Tuomas Gutmann, Michael U. Kaski, Samuel Corander, Jukka |
author_facet | Lintusaari, Jarno Blomstedt, Paul Rose, Brittany Sivula, Tuomas Gutmann, Michael U. Kaski, Samuel Corander, Jukka |
author_sort | Lintusaari, Jarno |
collection | PubMed |
description | Earlier research has suggested that approximate Bayesian computation (ABC) makes it possible to fit simulator-based intractable birth–death models to investigate communicable disease outbreak dynamics with accuracy comparable to that of exact Bayesian methods. However, recent findings have indicated that key parameters, such as the reproductive number R, may remain poorly identifiable with these models. Here we show that this identifiability issue can be resolved by taking into account disease-specific characteristics of the transmission process in closer detail. Using tuberculosis (TB) in the San Francisco Bay area as a case study, we consider a model that generates genotype data from a mixture of three stochastic processes, each with its own distinct dynamics and clear epidemiological interpretation. We show that our model allows for accurate posterior inferences about outbreak dynamics from aggregated annual case data with genotype information. As a byproduct of the inference, the model provides an estimate of the infectious population size at the time the data were collected. The acquired estimate is approximately two orders of magnitude smaller than assumed in earlier related studies, and it is much better aligned with epidemiological knowledge about active TB prevalence. Similarly, the reproductive number R related to the primary underlying transmission process is estimated to be nearly three times larger than previous estimates, which has a substantial impact on the interpretation of the fitted outbreak model. |
format | Online Article Text |
id | pubmed-10514576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-105145762023-09-23 Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models Lintusaari, Jarno Blomstedt, Paul Rose, Brittany Sivula, Tuomas Gutmann, Michael U. Kaski, Samuel Corander, Jukka Wellcome Open Res Method Article Earlier research has suggested that approximate Bayesian computation (ABC) makes it possible to fit simulator-based intractable birth–death models to investigate communicable disease outbreak dynamics with accuracy comparable to that of exact Bayesian methods. However, recent findings have indicated that key parameters, such as the reproductive number R, may remain poorly identifiable with these models. Here we show that this identifiability issue can be resolved by taking into account disease-specific characteristics of the transmission process in closer detail. Using tuberculosis (TB) in the San Francisco Bay area as a case study, we consider a model that generates genotype data from a mixture of three stochastic processes, each with its own distinct dynamics and clear epidemiological interpretation. We show that our model allows for accurate posterior inferences about outbreak dynamics from aggregated annual case data with genotype information. As a byproduct of the inference, the model provides an estimate of the infectious population size at the time the data were collected. The acquired estimate is approximately two orders of magnitude smaller than assumed in earlier related studies, and it is much better aligned with epidemiological knowledge about active TB prevalence. Similarly, the reproductive number R related to the primary underlying transmission process is estimated to be nearly three times larger than previous estimates, which has a substantial impact on the interpretation of the fitted outbreak model. F1000 Research Limited 2019-08-30 /pmc/articles/PMC10514576/ /pubmed/37744419 http://dx.doi.org/10.12688/wellcomeopenres.15048.2 Text en Copyright: © 2019 Lintusaari J et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Method Article Lintusaari, Jarno Blomstedt, Paul Rose, Brittany Sivula, Tuomas Gutmann, Michael U. Kaski, Samuel Corander, Jukka Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models |
title | Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models |
title_full | Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models |
title_fullStr | Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models |
title_full_unstemmed | Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models |
title_short | Resolving outbreak dynamics using approximate Bayesian computation for stochastic birth–death models |
title_sort | resolving outbreak dynamics using approximate bayesian computation for stochastic birth–death models |
topic | Method Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514576/ https://www.ncbi.nlm.nih.gov/pubmed/37744419 http://dx.doi.org/10.12688/wellcomeopenres.15048.2 |
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