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Finding Instability in Biological Models

机译:在生物模型中发现不稳定性

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摘要

The stability of biological models is an important test for establishing their soundness and accuracy. Stability in biological systems represents the ability of a robust system to always return to homeosta-sis. In recent work, modular approaches for proving stability have been found to be swift and scalable. If stability is however not proved, the currently available techniques apply an exhaustive search through the unstable state space to find loops. This search is frequently prohibitively computationally expensive, limiting its usefulness. Here we present a new modular approach eliminating the need for an exhaustive search for loops. Using models of biological systems we show that the technique finds loops significantly faster than brute force approaches. Furthermore, for a subset of stable systems which are resistant to modular proofs, we observe a speed up of up to 3 orders of magnitude as the exhaustive searches for loops which cause instability are avoided. With our new procedure we are able to prove instability and stability in a number of realistic biological models, including adaptation in bacterial chemotaxis, the lambda phage lysogeny/lysis switch, voltage gated channel opening and cAMP oscillations in the slime mold Dictyostelium discoideum. This new approach will support the development of new tools for biomedicine.
机译:生物学模型的稳定性是确定其健全性和准确性的重要测试。生物系统中的稳定性代表了强大的系统始终能够恢复稳态的能力。在最近的工作中,已经证明用于证明稳定性的模块化方法是快速且可扩展的。但是,如果没有证明稳定性,则当前可用的技术将在不稳定状态空间中进行详尽的搜索,以找到循环。该搜索经常在计算上非常昂贵,从而限制了其实用性。在这里,我们提出了一种新的模块化方法,无需彻底搜索循环。使用生物系统的模型,我们证明了该技术发现循环的速度比蛮力方法快得多。此外,对于可抵抗模块化证明的稳定系统的子集,由于避免了对导致不稳定性的回路的详尽搜索,我们观察到速度可提高3个数量级。通过我们的新程序,我们能够证明许多现实的生物学模型的不稳定性和稳定性,包括细菌趋化性的适应性,λ噬菌体的溶源/裂解开关,电压控制的通道打开以及粘液霉菌盘基网柄菌中的cAMP振荡。这种新方法将支持生物医学新工具的开发。

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