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Dynamic Bayesian network in infectious diseases surveillance: a simulation study
The surveillance of infectious diseases relies on the identification of dynamic relations between the infectious diseases and corresponding influencing factors. However, the identification task confronts with two practical challenges: small sample size and delayed effect. To overcome both challenges...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637193/ https://www.ncbi.nlm.nih.gov/pubmed/31316113 http://dx.doi.org/10.1038/s41598-019-46737-0 |
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author | Zhang, Tao Ma, Yue Xiao, Xiong Lin, Yun Zhang, Xingyu Yin, Fei Li, Xiaosong |
author_facet | Zhang, Tao Ma, Yue Xiao, Xiong Lin, Yun Zhang, Xingyu Yin, Fei Li, Xiaosong |
author_sort | Zhang, Tao |
collection | PubMed |
description | The surveillance of infectious diseases relies on the identification of dynamic relations between the infectious diseases and corresponding influencing factors. However, the identification task confronts with two practical challenges: small sample size and delayed effect. To overcome both challenges to imporve the identification results, this study evaluated the performance of dynamic Bayesian network(DBN) in infectious diseases surveillance. Specifically, the evaluation was conducted by two simulations. The first simulation was to evaluate the performance of DBN by comparing it with the Granger causality test and the least absolute shrinkage and selection operator (LASSO) method; and the second simulation was to assess how the DBN could improve the forecasting ability of infectious diseases. In order to make both simulations close to the real-world situation as much as possible, their simulation scenarios were adapted from real-world studies, and practical issues such as nonlinearity and nuisance variables were also considered. The main simulation results were: ① When the sample size was large (n = 340), the true positive rates (TPRs) of DBN (≥98%) were slightly higher than those of the Granger causality method and approximately the same as those of the LASSO method; the false positive rates (FPRs) of DBN were averagely 46% less than those of the Granger causality test, and 22% less than those of the LASSO method. ② When the sample size was small, the main problem was low TPR, which would be further aggravated by the issues of nonlinearity and nuisance variables. In the worst situation (i.e., small sample size, nonlinearity and existence of nuisance variables), the TPR of DBN declined to 43.30%. However, it was worth noting that such decline could also be found in the corresponding results of Granger causality test and LASSO method. ③ Sample size was important for identifying the dynamic relations among multiple variables, in this case, at least three years of weekly historical data were needed to guarantee the quality of infectious diseases surveillance. ④ DBN could improve the foresting results through reducing forecasting errors by 7%. According to the above results, DBN is recommended to improve the quality of infectious diseases surveillance. |
format | Online Article Text |
id | pubmed-6637193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66371932019-07-25 Dynamic Bayesian network in infectious diseases surveillance: a simulation study Zhang, Tao Ma, Yue Xiao, Xiong Lin, Yun Zhang, Xingyu Yin, Fei Li, Xiaosong Sci Rep Article The surveillance of infectious diseases relies on the identification of dynamic relations between the infectious diseases and corresponding influencing factors. However, the identification task confronts with two practical challenges: small sample size and delayed effect. To overcome both challenges to imporve the identification results, this study evaluated the performance of dynamic Bayesian network(DBN) in infectious diseases surveillance. Specifically, the evaluation was conducted by two simulations. The first simulation was to evaluate the performance of DBN by comparing it with the Granger causality test and the least absolute shrinkage and selection operator (LASSO) method; and the second simulation was to assess how the DBN could improve the forecasting ability of infectious diseases. In order to make both simulations close to the real-world situation as much as possible, their simulation scenarios were adapted from real-world studies, and practical issues such as nonlinearity and nuisance variables were also considered. The main simulation results were: ① When the sample size was large (n = 340), the true positive rates (TPRs) of DBN (≥98%) were slightly higher than those of the Granger causality method and approximately the same as those of the LASSO method; the false positive rates (FPRs) of DBN were averagely 46% less than those of the Granger causality test, and 22% less than those of the LASSO method. ② When the sample size was small, the main problem was low TPR, which would be further aggravated by the issues of nonlinearity and nuisance variables. In the worst situation (i.e., small sample size, nonlinearity and existence of nuisance variables), the TPR of DBN declined to 43.30%. However, it was worth noting that such decline could also be found in the corresponding results of Granger causality test and LASSO method. ③ Sample size was important for identifying the dynamic relations among multiple variables, in this case, at least three years of weekly historical data were needed to guarantee the quality of infectious diseases surveillance. ④ DBN could improve the foresting results through reducing forecasting errors by 7%. According to the above results, DBN is recommended to improve the quality of infectious diseases surveillance. Nature Publishing Group UK 2019-07-17 /pmc/articles/PMC6637193/ /pubmed/31316113 http://dx.doi.org/10.1038/s41598-019-46737-0 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Zhang, Tao Ma, Yue Xiao, Xiong Lin, Yun Zhang, Xingyu Yin, Fei Li, Xiaosong Dynamic Bayesian network in infectious diseases surveillance: a simulation study |
title | Dynamic Bayesian network in infectious diseases surveillance: a simulation study |
title_full | Dynamic Bayesian network in infectious diseases surveillance: a simulation study |
title_fullStr | Dynamic Bayesian network in infectious diseases surveillance: a simulation study |
title_full_unstemmed | Dynamic Bayesian network in infectious diseases surveillance: a simulation study |
title_short | Dynamic Bayesian network in infectious diseases surveillance: a simulation study |
title_sort | dynamic bayesian network in infectious diseases surveillance: a simulation study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637193/ https://www.ncbi.nlm.nih.gov/pubmed/31316113 http://dx.doi.org/10.1038/s41598-019-46737-0 |
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