TY - JOUR
T1 - Fast screening framework for infection control scenario identification
AU - Kakimoto, Yohei
AU - Omae, Yuto
AU - Toyotani, Jun
AU - Takahashi, Hirotaka
N1 - Publisher Copyright:
© 2022 the Author(s).
PY - 2022
Y1 - 2022
N2 - Due to the emergence of the novel coronavirus disease, many recent studies have investigated prediction methods for infectious disease transmission. This paper proposes a framework to quickly screen infection control scenarios and identify the most effective scheme for reducing the number of infected individuals. Analytical methods, as typified by the SIR model, can conduct trialand- error verification with low computational costs; however, they must be reformulated to introduce additional constraints, and thus are inappropriate for case studies considering detailed constraint parameters. In contrast, multi-agent system (MAS) simulators introduce detailed parameters but incur high computation costs per simulation, making them unsuitable for extracting effective measures. Therefore, we propose a framework that implements an MAS for constructing a training dataset, and then trains a support vector regression (SVR) model to obtain effective measure results. The proposed framework overcomes the weaknesses of conventional methods to produce effective control measure recommendations. The constructed SVR model was experimentally verified by comparing its performance on datasets with expected and unexpected outputs. Although datasets producing an unexpected output decreased the prediction accuracy, by removing randomness from the training dataset, the accuracy of the proposed method was still high in these cases. High-precision predictions of the MAS-based simulation output were obtained for both test datasets in under one second of the computational time. Furthermore, the experimental results establish that the proposed framework can obtain intuitively correct outputs for unknown inputs, and produces suffciently high-precision prediction with lower computation costs than an existing method.
AB - Due to the emergence of the novel coronavirus disease, many recent studies have investigated prediction methods for infectious disease transmission. This paper proposes a framework to quickly screen infection control scenarios and identify the most effective scheme for reducing the number of infected individuals. Analytical methods, as typified by the SIR model, can conduct trialand- error verification with low computational costs; however, they must be reformulated to introduce additional constraints, and thus are inappropriate for case studies considering detailed constraint parameters. In contrast, multi-agent system (MAS) simulators introduce detailed parameters but incur high computation costs per simulation, making them unsuitable for extracting effective measures. Therefore, we propose a framework that implements an MAS for constructing a training dataset, and then trains a support vector regression (SVR) model to obtain effective measure results. The proposed framework overcomes the weaknesses of conventional methods to produce effective control measure recommendations. The constructed SVR model was experimentally verified by comparing its performance on datasets with expected and unexpected outputs. Although datasets producing an unexpected output decreased the prediction accuracy, by removing randomness from the training dataset, the accuracy of the proposed method was still high in these cases. High-precision predictions of the MAS-based simulation output were obtained for both test datasets in under one second of the computational time. Furthermore, the experimental results establish that the proposed framework can obtain intuitively correct outputs for unknown inputs, and produces suffciently high-precision prediction with lower computation costs than an existing method.
KW - fast screening framework
KW - identifying effective scheme
KW - infection control
KW - multi-agent system
KW - support vector regression
UR - http://www.scopus.com/inward/record.url?scp=85136461935&partnerID=8YFLogxK
U2 - 10.3934/mbe.2022574
DO - 10.3934/mbe.2022574
M3 - Article
C2 - 36653999
AN - SCOPUS:85136461935
SN - 1547-1063
VL - 19
SP - 12316
EP - 12333
JO - Mathematical Biosciences and Engineering
JF - Mathematical Biosciences and Engineering
IS - 12
ER -