Centre for Health Informatics and Multiprofessional Education, University College London London, UK ; Auckland Bioengineering Institute, University of Auckland Auckland, New Zealand.
Auckland Bioengineering Institute, University of Auckland Auckland, New Zealand.
Front Physiol. 2015 Feb 24;6:24. doi: 10.3389/fphys.2015.00024. eCollection 2015.
A key challenge for the physiology modeling community is to enable the searching, objective comparison and, ultimately, re-use of models and associated data that are interoperable in terms of their physiological meaning. In this work, we outline the development of a workflow to modularize the simulation of tissue-level processes in physiology. In particular, we show how, via this approach, we can systematically extract, parcellate and annotate tissue histology data to represent component units of tissue function. These functional units are semantically interoperable, in terms of their physiological meaning. In particular, they are interoperable with respect to [i] each other and with respect to [ii] a circuitboard representation of long-range advective routes of fluid flow over which to model long-range molecular exchange between these units. We exemplify this approach through the combination of models for physiology-based pharmacokinetics and pharmacodynamics to quantitatively depict biological mechanisms across multiple scales. Links to the data, models and software components that constitute this workflow are found at http://open-physiology.org/.
对生理学建模社区来说,一个关键挑战是能够搜索、客观比较并最终重用在生理学意义上可互操作的模型和相关数据。在这项工作中,我们概述了开发一个工作流程的过程,以实现组织水平过程模拟的模块化。特别是,我们展示了如何通过这种方法,我们可以系统地提取、分割和注释组织组织学数据,以表示组织功能的组成单元。这些功能单元在生理学意义上是语义可互操作的。特别是,它们在[一]彼此之间以及[二]长程扩散流的电路板表示之间是可互操作的,以在这些单元之间建模长程分子交换。我们通过结合基于生理学的药代动力学和药效动力学模型来举例说明这种方法,以定量描述多个尺度上的生物学机制。构成该工作流程的数据、模型和软件组件的链接可在 http://open-physiology.org/ 找到。