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Modeling Gene Regulatory Subnetworks from Time Course Gene Expression Data

机译:从时程基因表达数据建模基因调控子网

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Identifying gene regulatory network (GRN) from time course gene expression data has attracted more and more attentions. Due to the computational complexity, most approaches for GRN econstruction are limited on a small number of genes and low connectivity of the underlying networks. These approaches can only identify a single network for a given set of genes. However, for a large-scale gene network, there might exist multiple potential sub-networks, in which genes are only functionally related to thers in the sub-networks. In this paper, we propose an efficient algorithm for identifying multiple sub-networks from gene expression data by incorporating community structure information into GRN inference. The proposed algorithm iteratively solves two optimization problems, and thus promisingly applies to large-scale GRNs. Experimental studies on synthetic datasets validate the effectiveness of the proposed algorithm in the inference of sub-networks.
机译:从时程基因表达数据鉴定基因调控网络(GRN)已引起越来越多的关注。由于计算复杂性,大多数用于GRN构建的方法都限于少数基因和底层网络的低连通性。这些方法只能为给定的一组基因识别单个网络。但是,对于大规模的基因网络,可能存在多个潜在的子网络,其中基因在功能上仅与子网络中的其他功能相关。在本文中,我们提出了一种有效的算法,通过将社区结构信息纳入GRN推理,可以从基因表达数据中识别多个子网。所提出的算法迭代地解决了两个优化问题,因此有望应用于大规模GRN。综合数据集的实验研究证明了该算法在子网推理中的有效性。

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