利用基于sat的有界模型检验寻找同步多值网络中的吸引子

E. Dubrova, Ming Liu, M. Teslenko
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引用次数: 11

摘要

同步多值网络是活细胞基因调控网络的离散空间离散时间模型。在该模型中,细胞类型由网络状态转移图中的循环表示,称为吸引子。当研究疾病或突变对细胞的影响时,每次在模型中注入错误时,都必须重新计算吸引子。这激发了对寻找吸引子算法的研究。现有的基于决策图的方法由于对决策图的内存需求过大而容量有限。基于仿真的方法可以应用于更大的网络,但是,它们是不完整的。我们提出了一种利用基于sat的有界模型检验来寻找吸引子的算法。我们的模型检查方法利用网络模型的确定性来减少运行时间。虽然将模型检查应用于基因调控网络分析的想法并不新鲜,但据我们所知,我们是第一个将其用于计算模型中所有吸引子的人。通过分析7个真实生物过程的网络模型和35000个随机生成的4值网络,对该算法的有效性进行了评价。结果表明,我们的方法有可能处理比目前可能的更大数量级的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Finding Attractors in Synchronous Multiple-Valued Networks Using SAT-Based Bounded Model Checking
Synchronous multiple-valued networks are a discrete-space discrete-time model of the gene regulatory network of living cells. In this model, cell types are represented by the cycles in the state transition graph of a network, called attractors. When the effect of a disease or a mutation on a cell is studied, attractors have to be re-computed each time a fault is injected in the model. This motivates research on algorithms for finding attractors. Existing decision diagram-based approaches have limited capacity due to the excessive memory requirements of decision diagrams. Simulation-based approaches can be applied to larger networks, however, they are incomplete. We present an algorithm for finding attractors which uses a SAT-based bounded model checking. Our model checking approach exploits the deterministic nature of the network model to reduce runtime. Although the idea of applying model checking to the analysis of gene regulatory networks is not new, to our best knowledge, we are the first to use it for computing all attractors in a model. The efficiency of the presented algorithm is evaluated by analyzing 7 networks models of real biological processes as well as 35.000 randomly generated 4-valued networks. The results show that our approach has a potential to handle an order of magnitude larger models than currently possible.
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