2018
DOI: 10.1101/267070
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PhysiBoSS: a multi-scale agent based modelling framework integrating physical dimension and cell signalling

Abstract: Due to the complexity of biological systems, their heterogeneity, and the internal regulation of each cell and its surrounding, mathematical models that take into account cell signalling, cell population behaviour and the extracellular environment are particularly helpful to understand such complex systems. However, very few of these tools, freely available and computationally efficient, are currently available. To fill this gap, we present here our open-source software, PhysiBoSS, which is built on two availa… Show more

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Cited by 8 publications
(2 citation statements)
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References 81 publications
(114 reference statements)
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“…Over the years, a number of computational tools forf implementing ABMs have been developed, including advanced methods for incorporating both inter-and intra-cellular interactions to simulate the global dynamics of multicellular systems (22) (23). Here, we present an ABM implemented in Netlogo (24) (25) aiming to reproduce monocyte differentiation and polarization into NLC upon contact with B-CLL cells in an in-vitro environment.…”
Section: Introductionmentioning
confidence: 99%
“…Over the years, a number of computational tools forf implementing ABMs have been developed, including advanced methods for incorporating both inter-and intra-cellular interactions to simulate the global dynamics of multicellular systems (22) (23). Here, we present an ABM implemented in Netlogo (24) (25) aiming to reproduce monocyte differentiation and polarization into NLC upon contact with B-CLL cells in an in-vitro environment.…”
Section: Introductionmentioning
confidence: 99%
“…Previous 3D spatial models of human solid tumors have reflected some aspects of realistic phenotypes. However, these models have not explicitly included lymphocytes, stroma, and macrophages (8,9), which are key players in colorectal cancer (10), or have incorporated some parts of the microenvironment without clinical validation and in a computationally expensive way (11). To our knowledge, there is currently no computational model of tumor growth that encompasses all relevant aspects of the TME and, at the same time, runs fast enough to be fitted to clinicopathologic data on a per-patient basis in thousands of model runs, which is a requirement for drug screening and other clinically relevant applications.…”
Section: Introductionmentioning
confidence: 99%