基于关联推理和传递熵估计的模型识别

C. Damiani, P. Lecca
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引用次数: 6

摘要

生物网络推理利用数学方法从观测数据中推断出生物化学相互作用网络的拓扑结构。最近,许多努力都是为了实现这一目标,越来越多的文献提出了新的推理数学模型。然而,这仍然是一项具有挑战性的任务,需要结合不同的方法来克服每个单一程序的局限性。在这项工作中,我们提出了三种方法来推断从反应物的丰度时间序列的生化网络的结构。第一种方法将物种间时滞相关性的评估与模型校准的概率方法相结合。第二种方法估计传递熵来检测时间序列之间的因果关系。第三种方法是将基于传递熵的方法与参数估计的概率模型相结合。我们讨论了这三种方法的动机、优势和局限性,并在实验验证的代谢网络模型生成的数据上展示了它们的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Model Identification Using Correlation-Based Inference and Transfer Entropy Estimation
Biological network inference makes use of mathematical methods to deduce the topology of networks of biochemical interactions from observational data. Recently, many efforts have been directed towards the achievement of this goal, and an increasing literature is proposing new mathematical models of inference. However, this still remains a challenging task, requiring a combination of different methods in order to overcome the limitations of each single procedure. In this work, we propose three methods to infer the structure of a biochemical network from the abundance of reactants time series. The first method combines the evaluation of the time-lagged correlation between species with a probabilistic method of model calibration. The second method estimates the transfer entropy to detect the causal relationships between time series. The third method is a combination of the transfer entropy-based method with the probabilistic model of parameter estimation. We argue the motivations, the advantages and the limitations of the three methods, and we present their performances on data generated from models of experimentally validated metabolic networks.
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