Abstract
Agent-based models (ABM) are widely used to study immune systems, providing a procedural and interactive view of the underlying system. The interaction of components and the behavior of individual objects is described procedurally as a function of the internal states and the local interactions, which are often stochastic in nature. Such models typically have complex structures and consist of a large number of modeling parameters. Determining the key modeling parameters which govern the outcomes of the system is very challenging. Sensitivity analysis plays a vital role in quantifying the impact of modeling parameters in massively interacting systems, including large complex ABM. The high computational cost of executing simulations impedes running experiments with exhaustive parameter settings. Existing techniques of analyzing such a complex system typically focus on local sensitivity analysis, i.e. one parameter at a time, or a close "neighborhood" of particular parameter settings. However, such methods are not adequate to measure the uncertainty and sensitivity of parameters accurately because they overlook the global impacts of parameters on the system. In this article, we develop novel experimental design and analysis techniques to perform both global and local sensitivity analysis of large-scale ABMs. The proposed method can efficiently identify the most significant parameters and quantify their contributions to outcomes of the system. We demonstrate the proposed methodology for ENteric Immune SImulator (ENISI), a large-scale ABM environment, using a computational model of immune responses to Helicobacter pylori colonization of the gastric mucosa.
Original language | English |
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Article number | e0136139 |
Journal | PLoS ONE |
Volume | 10 |
Issue number | 9 |
DOIs | |
State | Published - Sep 1 2015 |
Externally published | Yes |
Funding
We thank our external collaborators and members of the Network Dynamics and Simulation Science Laboratory (NDSSL) and the Nutritional Immunology and Molecular Medicine Laboratory (NIMML, http://www.nimml.org ) for their suggestions and comments. This work has been partially supported by Defense Threat Reduction Agency (DTRA)—R&D (HPC) Award No. HDTRA1-09-1-0017, DTRA—Validation Award No. HDTRA1-11-1-0016, DTRA—Comprehensive National Incident Management System (CNIMS) Award No. HDRTA1-11-D-0016-0001, National Science Foundation (NSF) PetaApps Grant OCI-0904844, NSF Network Science and Engineering (NetSE) Grant CNS-1011769, NSF Software Development for Cyberinfrastructure (SDCI) Grant OCI-1032677, National Institutes of Health (NIH) MIDAS project 2U01GM070694-7 and National Institute of Allergy and Infectious Diseases (NIAID) & NIH project HHSN272201000056C.
Funders | Funder number |
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NSF Network Science and Engineering | |
NSF Software Development for Cyberinfrastructure | |
National Institute of Allergy and Infectious Diseases | |
National Institutes of Health | |
NetSE | CNS-1011769 |
SDCI | OCI-1032677 |
National Science Foundation | OCI-0904844 |
National Institutes of Health | |
National Institute of General Medical Sciences | U01GM070694 |
National Institute of Allergy and Infectious Diseases | HHSN272201000056C |
Defense Threat Reduction Agency | HDRTA1-11-D-0016-0001, HDTRA1-09-1-0017, HDTRA1-11-1-0016 |