首页> 外文会议>Intelligent Systems, Modelling and Simulation (ISMS 2010), 2010 >Correlation-Based Network Inference and Modelling in Systems Biology: The NF-kappa B Signalling Network Case Study
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Correlation-Based Network Inference and Modelling in Systems Biology: The NF-kappa B Signalling Network Case Study

机译:系统生物学中基于相关性的网络推理和建模:NF-kappa信令网络案例研究

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It is currently attracting the interest of theoretical biologists, biochemicists and experimentalists to attempt to deduce the structure of biochemical networks "ab initio" from routinely available experimental data. The recent advances in systems biology have been driven by the methods that generate in vivo time-course data characterizing biochemical network interactions. Such data can be used for inferring a model structure and its parameters in order to examine the dynamic behavior of biological processes on a systemic level. We present here a new correlation-based approach to network inference, whose most attractive feature is that information can be extracted from the observed data with little a priori knowledge of the underlying mechanisms. Our method introduces a new correlation metric based on a Voronoi tessellation of the variable space and infers correlations among stationary time series data of reactant concentrations. These correlations can be used to reveal dependencies between variables, as well as connectivity between species. The method has been applied to a real case study: the binding kinetics of the enzyme inhibitor kappa B kinase to its substrate inhibitor kappa B alpha, whose interaction is an integral part of the transduction of signals in the NF-kappa B signalling pathway.
机译:当前,试图从常规可获得的实验数据推论“从头开始”的生化网络结构吸引了理论生物学家,生化学家和实验学家的兴趣。系统生物学的最新进展受到生成表征生化网络相互作用的体内时程数据的方法的驱动。此类数据可用于推断模型结构及其参数,以便在系统水平上检查生物过程的动态行为。我们在这里提出了一种基于相关性的网络推理新方法,其最吸引人的特点是可以在几乎不了解底层机制的前提下从观测数据中提取信息。我们的方法基于可变空间的Voronoi细分引入了一种新的相关度量,并推断出反应物浓度的固定时间序列数据之间的相关性。这些相关性可以用来揭示变量之间的依存关系,以及物种之间的连通性。该方法已应用于实际案例研究:酶抑制剂kappa B激酶与其底物抑制剂kappa B alpha的结合动力学,其相互作用是NF-kappa B信号通路中信号转导的组成部分。

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