Learning-accelerated discovery of immune-tumour interactions
dc.contributor.author | Ozik, J | |
dc.contributor.author | Collier, N | |
dc.contributor.author | Heiland, R | |
dc.contributor.author | An, G | |
dc.contributor.author | Macklin, Paul | |
dc.date.accessioned | 2025-02-20T15:58:44Z | |
dc.date.available | 2025-02-20T15:58:44Z | |
dc.date.issued | 2019-06-07 | |
dc.description.abstract | We present an integrated framework for enabling dynamic exploration of design spaces for cancer immunotherapies with detailed dynamical simulation models on high-performance computing resources. Our framework combines PhysiCell, an open source agent-based simulation platform for cancer and other multicellular systems, and EMEWS, an open source platform for extreme-scale model exploration. We build an agent-based model of immunosurveillance against heterogeneous tumours, which includes spatial dynamics of stochastic tumour–immune contact interactions. We implement active learning and genetic algorithms using high-performance computing workflows to adaptively sample the model parameter space and iteratively discover optimal cancer regression regions within biological and clinical constraints. | |
dc.identifier.citation | Ozik, J, et al. "Learning-accelerated discovery of immune-tumour interactions." Molecular Systems Design & Engineering, vol. 4, no. 4, 2019-06-07, https://doi.org/10.1039/c9me00036d. | |
dc.identifier.issn | 2058-9689 | |
dc.identifier.other | BRITE 6026 | |
dc.identifier.uri | https://hdl.handle.net/2022/31768 | |
dc.language.iso | en | |
dc.relation.isversionof | https://doi.org/10.1039/c9me00036d | |
dc.relation.isversionof | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690424 | |
dc.relation.journal | Molecular Systems Design & Engineering | |
dc.title | Learning-accelerated discovery of immune-tumour interactions |
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