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首页> 外文期刊>Journal of the Royal Society Interface >Accurate and efficient discretizations for stochastic models providing near agent-based spatial resolution at low computational cost
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Accurate and efficient discretizations for stochastic models providing near agent-based spatial resolution at low computational cost

机译:在低计算成本下提供基于代理的空间分辨率附近的随机模型的准确和有效的离散化

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摘要

Understanding how cells proliferate, migrate and die in various environments is essential in determining how organisms develop and repair themselves. Continuum mathematical models, such as the logistic equation and the Fisher-Kolmogorov equation, can describe the global characteristics observed in commonly used cell biology assays, such as proliferation and scratch assays. However, these continuum models do not account for single-cell-level mechanics observed in high-throughput experiments. Mathematical modelling frameworks that represent individual cells, often called agent-based models, can successfully describe key single-cell-level features of these assays but are computationally infeasible when dealing with large populations. In this work, we propose an agent-based model with crowding effects that is computationally efficient and matches the logistic and Fisher-Kolmogorov equations in parameter regimes relevant to proliferation and scratch assays, respectively. This stochastic agent-based model allows multiple agents to be contained within compartments on an underlying lattice, thereby reducing the computational storage compared to existing agent-based models that allow one agent per site only. We propose a systematic method to determine a suitable compartment size. Implementing this compartment-based model with this compartment size provides a balance between computational storage, local resolution of agent behaviour and agreement with classical continuum descriptions.
机译:了解细胞在各种环境中如何激增,迁移和死亡对于确定有机体如何发展和修复自己是必不可少的。连续体数学模型,例如物流方程和Fisher-Kolmogorov方程,可以描述在常用的细胞生物学测定中观察到的全局特征,例如增殖和划痕测定。然而,这些连续模型不考虑在高通量实验中观察到的单细胞级机制。数学建模框架,代表各个单元格,通常称为基于代理的模型,可以成功描述这些测定的关键单细胞级别特征,而是在处理大群中的计算地是可行的。在这项工作中,我们提出了一种基于代理的模型,该模型具有挤出效应,该挤压效应分别在计算上有效,并将逻辑和Fisher-Kolmogorov方程分别与增殖和划痕测定相关的参数制度匹配。基于随机代理的模型允许多个代理包含在底层晶格上的隔间内,从而与每个站点允许一个代理的基于代理的模型相比减少计算存储。我们提出了一种系统的方法来确定合适的隔间大小。使用此隔间大小实现基于隔间的模型在计算存储,代理行为的本地分辨率和与经典连续内描述协议之间提供平衡。

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