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A method for estimating Hill function-based dynamic models of gene regulatory networks

机译:一种基于希尔函数的基因调控网络动态模型的估计方法

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摘要

Gene regulatory networks (GRNs) are quite large and complex. To better understand and analyse GRNs, mathematical models are being employed. Different types of models, such as logical, continuous and stochastic models, can be used to describe GRNs. In this paper, we present a new approach to identify continuous models, because they are more suitable for large number of genes and quantitative analysis. One of the most promising techniques for identifying continuous models of GRNs is based on Hill functions and the generalized profiling method (GPM). The advantage of this approach is low computational cost and insensitivity to initial conditions. In the GPM, a constrained nonlinear optimization problem has to be solved that is usually underdetermined. In this paper, we propose a new optimization approach in which we reformulate the optimization problem such that constraints are embedded implicitly in the cost function. Moreover, we propose to split the unknown parameter in two sets based on the structure of Hill functions. These two sets are estimated separately to resolve the issue of the underdetermined problem. As a case study, we apply the proposed technique on the SOS response in Escherichia coli and compare the results with the existing literature.
机译:基因调控网络(GRN)非常庞大且复杂。为了更好地理解和分析GRN,正在使用数学模型。可以使用不同类型的模型(例如逻辑模型,连续模型和随机模型)来描述GRN。在本文中,我们提出了一种识别连续模型的新方法,因为它们更适合大量基因和定量分析。用于识别GRN连续模型的最有前途的技术之一是基于Hill函数和广义剖析方法(GPM)。这种方法的优点是计算成本低,并且对初始条件不敏感。在GPM中,必须解决通常无法确定的约束非线性优化问题。在本文中,我们提出了一种新的优化方法,在该方法中,我们重新制定了优化问题,以便将约束隐式地嵌入到成本函数中。此外,我们建议根据希尔函数的结构将未知参数分为两组。分别估计这两个集合以解决不确定问题的问题。作为案例研究,我们将提出的技术应用于大肠杆菌中的SOS反应,并将结果与​​现有文献进行比较。

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