Abstract

The accumulated omic data provides an opportunity to exploit the mechanisms of cancers and poses a challenge for their integrative analysis. Although extensive efforts have been devoted to address this issue, the current algorithms result in undesirable performance because of the complexity of patterns and heterogeneity of data. In this study, the ultimate goal is to propose an effective and efficient algorithm (called NMF-DEC) to identify clusters by integrating the interactome and transcriptome data. By treating the expression profiles of genes as attributes of vertices in the gene interaction networks, we transform the integrative analysis of omic data into clustering of attributed networks. To circumvent the heterogeneity, we construct a similarity network for the attributes of genes and cast it into the common module detection problem in multi-layer networks. The NMF-DEC explores the relation between attributes and topological structure of networks by jointly factorizing the similarity and interaction networks with the same basis. In this optimization, the interaction network is dynamically updated and the information of attributes is dynamically incorporated, providing a better strategy to characterize the structure of modules in attributed networks. Extensive experiments indicate that compared with state-of-the-art baselines, NMF-DEC is more accurate on social network, and show better performance on cancer attributed networks, implying the superiority of the proposed methods for the integrative analysis of omic data.

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