Pareto - epsilon-dominance和BioCAD建模的可识别解

C. Angione, Jole Costanza, Giovanni Carapezza, P. Lio’, Giuseppe Nicosia
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引用次数: 3

摘要

我们提出了一个框架来设计代谢途径,其中许多目标同时优化。这可以表征藻类和线粒体代谢模型中的能量特征。采用以epsilon-dominance和辨识性分析为驱动的多目标优化技术,实现了模型的优化设计和评估。通过放松Pareto优势,调节Pareto前沿逼近的粒度,允许具有鲁棒候选解的更快收敛过程。我们的框架也适用于黑盒分析,能够研究和优化任何用ode, DAEs, FBA和GPR建模的生物途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pareto epsilon-dominance and identifiable solutions for BioCAD modeling
We propose a framework to design metabolic pathways in which many objectives are optimized simultaneously. This allows to characterize the energy signature in models of algal and mitochondrial metabolism. The optimal design and assessment of the model is achieved through a multi-objective optimization technique driven by epsilon-dominance and identifiability analysis. A faster convergence process with robust candidate solutions is permitted by a relaxed Pareto dominance, regulating the granularity of the approximation of the Pareto front. Our framework is also suitable for black-box analysis, enabling to investigate and optimize any biological pathway modeled with ODEs, DAEs, FBA and GPR.
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