具有公平性的定性路径模型的模块化验证

P. Drábik, A. Maggiolo-Schettini, P. Milazzo, G. Pardini
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引用次数: 2

摘要

模块化验证是针对并发交互系统等复杂系统特性验证中经常遇到的状态爆炸问题而提出的一种技术。模块化方法基于这样一种观察,即感兴趣的属性通常只涉及系统的很小一部分。因此,可以构建简化模型,以近似整个系统行为,从而允许更有效的验证。生化途径可以看作是复杂的并发交互系统。因此,验证它们的属性通常在计算上非常昂贵,并且可以利用模块化方法。在本文中,我们开发了生化途径的模块化验证框架。我们认为生化途径是竞争分子资源的并行反应系统。模块化验证技术可以基于只包含涉及感兴趣的分子资源的反应的简化模型。为了正确描述系统行为,我们认为有必要考虑一个合适的公平概念,这是并发理论中一个成熟的概念,但在路径建模领域是新颖的。我们考虑的公平概念禁止反应的饥饿,也就是说,它确保一个无限经常被激活的反应不会总是损害另一个无限经常被激活的反应,导致后者永远不会发生。我们证明了该方法的正确性,并在Schoeberl等人的EGF受体诱导的MAP激酶级联模型上进行了验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modular Verification of Qualitative Pathway Models with Fairness
Modular verification is a technique used to face the state explosion problem often encountered in the verification of properties of complex systems such as concurrent interactive systems. The modular approach is based on the observation that properties of interest often concern a rather small portion of the system. As a consequence, reduced models can be constructed which approximate the overall system behaviour thus allowing more efficient verification. Biochemical pathways can be seen as complex concurrent interactive systems. Consequently, verification of their properties is often computationally very expensive and could take advantage of the modular approach. In this paper we develop a modular verification framework for biochemical pathways. We view biochemical pathways as concurrent systems of reactions competing for molecular resources. A modular verification technique could be based on reduced models containing only reactions involving molecular resources of interest. For a proper description of the system behaviour we argue that it is essential to consider a suitable notion of fairness, which is a well-established notion in concurrency theory but novel in the field of pathway modelling. The fairness notion we consider forbids starvation of reactions, namely it ensures that a reaction that is enabled infinitely often cannot always occur to the detriment of another infinitely often enabled reaction causing the latter to never occur. We prove the correctness of the approach and demonstrate it on the model of the EGF receptor-induced MAP kinase cascade by Schoeberl et al.
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