A tensor-based Markov chain method for module identification from multiple networks

Chenyang Shen, Shuqin Zhang, M. Ng
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引用次数: 2

Abstract

The interactions among different genes, proteins and other small molecules are becoming more and more significant and have been studied intensively nowadays. One general way that helps people understand these interactions is to analyze networks constructed from genes/proteins. In particular, module structure as a common property of most biological networks has drawn much attention of researchers from different fields. In most cases, biological networks can be corrupted by noise in the data and the corruption may cause mis-identification of module structure. Besides, some structure may be destroyed when improper experimental settings are built up. Thus module structure may be unstable when one single network is employed. In this paper, we consider employing multiple networks for consistent module detection in order to reduce the effect of noise and experimental setting. Instead of considering different networks separately, our idea is to combine multiple networks together by building them into tensor structure data. Then given any node as prior label information, tensor-based Markov chains are constructed iteratively for identification of the modules shared by the multiple networks. In addition, the proposed tensor-based Markov chain algorithm is capable of simultaneously evaluating the contribution from each network. It would be useful to measure the consistency of modules in the multiple networks. In the experiments, we test our method on two groups of gene co-expression networks from human beings. We also validate the modules identified by the proposed method.
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基于张量的马尔可夫链多网络模块识别方法
不同基因、蛋白质和其他小分子之间的相互作用越来越重要,目前已被深入研究。帮助人们理解这些相互作用的一个一般方法是分析由基因/蛋白质构成的网络。特别是模块结构作为大多数生物网络的共同特性,引起了不同领域研究者的广泛关注。在大多数情况下,生物网络可能会被数据中的噪声破坏,并且这种破坏可能导致模块结构的错误识别。此外,当实验设置不当时,一些结构可能会被破坏。因此,当采用单一网络时,模块结构可能不稳定。在本文中,我们考虑采用多个网络进行一致性模块检测,以减少噪声和实验环境的影响。我们的想法不是单独考虑不同的网络,而是通过构建张量结构数据将多个网络组合在一起。然后,给定任意节点作为先验标签信息,迭代构造基于张量的马尔可夫链来识别多个网络共享的模块。此外,提出的基于张量的马尔可夫链算法能够同时评估每个网络的贡献。这将有助于测量多个网络中模块的一致性。在实验中,我们在两组人类基因共表达网络上测试了我们的方法。我们还验证了该方法所识别的模块。
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