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Uncovering signal transduction networks from high-throughput data by integer linear programming

机译:通过整数线性编程从高通量数据中发现信号转导网络

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摘要

Signal transduction is an important process that transmits signals from the outside of a cell to the inside to mediate sophisticated biological responses. Effective computational models to unravel such a process by taking advantage of high-throughput genomic and proteomic data are needed to understand the essential mechanisms underlying the signaling pathways. In this article, we propose a novel method for uncovering signal transduction networks (STNs) by integrating protein interaction with gene expression data. Specifically, we formulate STN identification problem as an integer linear programming (ILP) model, which can be actually solved by a relaxed linear programming algorithm and is flexible for handling various prior information without any restriction on the network structures. The numerical results on yeast MAPK signaling pathways demonstrate that the proposed ILP model is able to uncover STNs or pathways in an efficient and accurate manner. In particular, the prediction results are found to be in high agreement with current biological knowledge and available information in literature. In addition, the proposed model is simple to be interpreted and easy to be implemented even for a large-scale system.
机译:信号转导是将信号从细胞外部传递到内部以介导复杂的生物反应的重要过程。需要有效的计算模型来利用高通量的基因组和蛋白质组数据来解开这一过程,以了解信号通路的基本机制。在本文中,我们提出了一种通过整合蛋白质相互作用与基因表达数据来揭示信号转导网络(STN)的新颖方法。具体来说,我们将STN识别问题公式化为整数线性规划(ILP)模型,该模型实际上可以通过宽松的线性规划算法来解决,并且可以灵活地处理各种先验信息,而对网络结构没有任何限制。酵母MAPK信号通路的数值结果表明,所提出的ILP模型能够有效,准确地发现STN或通路。特别地,发现预测结果与当前的生物学知识和文献中可获得的信息高度一致。另外,即使对于大规模系统,所提出的模型也易于解释并且易于实现。

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