在系统不变水平上实现心脏模型的自动理解和对齐

Samuel Huang, Madeline Diep, Kuk Jin Jang, E. Cherry, F. Fenton, R. Cleaveland, Mikael Lindvall, R. Mangharam, Adam Porter
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引用次数: 1

摘要

心律失常的研究促进了各种模型的发展,这些模型具有不同的配方和尺度,并为不同的目的而设计,每个模型都具有不同的配置空间。然而,当它们的上下文重叠时,这些模型应该能够表现出相同的行为。将模型配置为既支持这种上下文等价性,又显示预期的行为特征,可能是一项挑战。由于这个问题的复杂性,自动化是可取的。我们提出了一个旨在自动化理解和对齐心脏模型行为的框架。为了理解模型,我们挖掘具有给定配置的模型在执行时将显示的一组属性(不变量)。理解可以扩展到模型对齐:我们执行一个模型的理解,然后为第二个模型挖掘一组配置,其中每个模型都产生与第一个模型的不变量对齐的不变量。所研究的两个模型的构型空间不需要以任何方式相关联;相反,系统是通过它们各自表现出的系统不变量来进行比较的。我们将系统不变量建模为关联规则,这是一种在数据挖掘领域中得到充分研究的表示。我们将我们的方法应用于两个一维心脏组织模型。一个模型是著名的基于微分方程的Fenton-Karma模型,代表相互连接的心脏细胞的电生理,而另一个模型是心脏组织的时间自动机表示,旨在实现形式分析。我们证明了模型在激活率和路径电导方面的一致性。我们希望这种方法可以推广到心脏模型之外。
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Towards Automated Comprehension and Alignment of Cardiac Models at the System Invariant Level
The study of cardiac arrhythmias has spurred the development of models across a variety of formulations and scales and designed for different purposes, each with distinct configuration spaces. Nevertheless, these models should be able to exhibit equivalent behavior when their contexts overlap. Configuring models to both support this context equivalence and still exhibit intended behavioral characteristics can be challenging. Due to the complexity of this problem, automation can be desirable. We present a framework aimed at automating the comprehension and alignment of cardiac model behaviors. For model comprehension, we mine a set of properties (invariants) that a model with given configuration will exhibit when executed. Comprehension can be extended to model alignment: we perform comprehension of one model, and then mine a set of configurations for a second, each of which produces invariants aligned to the invariants of the first. The configuration spaces of the two models under study need not be related in any way; rather, the systems are compared by means of the system invariants that they each exhibit. We model system invariants as association rules, a well-studied representation used in the field of data mining. We apply our methodology to two one-dimensional models of cardiac tissue. One model is the well-known differential-equations-based Fenton-Karma model representing the electrophysiology of interconnected cardiac cells, while the other is a timed automaton representation of cardiac tissue designed to enable formal analysis. We demonstrate alignment of the models with respect to activation rates and path conductance. We expect this methodology can be generalized beyond cardiac models.
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