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Continuous Time Bayesian Networks for Gene Network Reconstruction: A Comparative Study on Time Course Data

机译:连续时间贝叶斯网络用于基因网络重构:时程数据的比较研究

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Dynamic aspects of regulatory networks are typically investigated by measuring relevant variables at multiple points in time. Current state-of-the-art approaches for gene network reconstruction directly build on such data, making the strong assumption that the system evolves in a synchronous fashion and in discrete time. However, omics data generated with increasing time-course granularity allow to model gene networks as systems whose state evolves in continuous time, thus improving the model's expressiveness. In this work continuous time Bayesian networks are proposed as a new approach for regulatory network reconstruction from time-course expression data. Their performance is compared to that of two state-of-the-art methods: dynamic Bayesian networks and Granger causality. The comparison is accomplished using both simulated and experimental data. Continuous time Bayesian networks achieve the highest F-measure on both datasets. Furthermore, precision, recall and F-measure degrade in a smoother way than those of dynamic Bayesian networks and Granger causality, when the complexity of the gene regulatory network increases.
机译:通常通过在多个时间点测量相关变量来研究监管网络的动态方面。基因网络重建的当前最先进方法直接建立在这些数据上,有力的假设是该系统以同步方式和离散时间演进。但是,随着时间进程粒度的增加而生成的组学数据可以对基因网络进行建模,使其成为状态在连续时间内不断发展的系统,从而提高了模型的表达能力。在这项工作中,提出了连续时间贝叶斯网络作为从时程表达数据重建监管网络的新方法。将它们的性能与两种最新方法的性能进行比较:动态贝叶斯网络和Granger因果关系。比较是使用模拟和实验数据来完成的。连续时间贝叶斯网络在两个数据集上均实现了最高的F测度。此外,当基因调节网络的复杂性增加时,与动态贝叶斯网络和Granger因果关系相比,精确度,召回率和F度量会以更平滑的方式下降。

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