首页> 外文期刊>Communications in Information and Systems >BAYESIAN MODELS AND GIBBS SAMPLING STRATEGIES FOR LOCAL GRAPH ALIGNMENT AND MOTIF IDENTIFICATION IN STOCHASTIC BIOLOGICAL NETWORKS
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BAYESIAN MODELS AND GIBBS SAMPLING STRATEGIES FOR LOCAL GRAPH ALIGNMENT AND MOTIF IDENTIFICATION IN STOCHASTIC BIOLOGICAL NETWORKS

机译:随机生物网络中局部图形对齐和基元识别的贝叶斯模型和吉布斯采样策略

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摘要

With increasing amounts of interaction data collected by high-throughput techniques, understanding the structure and dynamics of biological networks becomes one of the central tasks in post-genomic molecular biology. Recent studies have shown that many biological networks contain a small set of "network motifs," which are suggested to be the basic cellular information-processing units in these networks. Nevertheless, most biological networks have stochastic nature, due to the intrinsic uncertainties of biological interactions and/or experimental noises accompanying the high-throughput data. The building blocks in these networks thus also have stochastic properties. In this paper, we study the problem of identifying stochastic network motifs that are derived from families of mutually similar but not necessarily identical patterns of interactions. Motivated by existing methods for detecting sequence motifs in biopolymer sequences, we establish Bayesian models for stochastic biological networks and develop a group of Gibbs sampling strategies for finding stochastic network motifs. The methods are applied to several available transcriptional regulatory networks and protein-protein interaction networks, and several stochastic network motifs are successfully identified.
机译:随着通过高通量技术收集的相互作用数据数量的增加,了解生物网络的结构和动力学成为后基因组分子生物学的中心任务之一。最近的研究表明,许多生物网络都包含一小组“网络主题”,这被认为是这些网络中基本的细胞信息处理单元。然而,由于伴随高通量数据的生物相互作用和/或实验性噪声的内在不确定性,大多数生物网络具有随机性。因此,这些网络中的构造块也具有随机属性。在本文中,我们研究识别随机网络图案的问题,这些图案是从相互相似但不一定相同的相互作用模式族中得出的。受用于检测生物聚合物序列中序列基序的现有方法的启发,我们建立了用于随机生物网络的贝叶斯模型,并开发了一组Gibbs采样策略来查找随机网络基序。将该方法应用于几种可用的转录调节网络和蛋白质-蛋白质相互作用网络,并成功鉴定了几种随机网络基序。

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  • 来源
    《Communications in Information and Systems》 |2009年第4期|347-370|共24页
  • 作者单位

    MOE Key Laboratory of Bioinformatics, Bioinformatics Division, TNLIST/Department of Automation, Tsinghua University, Beijing 100084, China;

    rnMolecular and Computational Biology Program, University of Southern California, Los Angeles,CA 90089-2910;

    rnMolecular and Computational Biology Program,University of Southern California. RRI 201, 1050 Childs Way, Los Angeles, CA 90089-2910;

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