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Refine gene functional similarity network based on interaction networks.

ABSTRACT: BACKGROUND:In recent years, biological interaction networks have become the basis of some essential study and achieved success in many applications. Some typical networks such as protein-protein interaction networks have already been investigated systematically. However, little work has been available for the construction of gene functional similarity networks so far. In this research, we will try to build a high reliable gene functional similarity network to promote its further application. RESULTS:Here, we propose a novel method to construct and refine the gene functional similarity network. It mainly contains three steps. First, we establish an integrated gene functional similarity networks based on different functional similarity calculation methods. Then, we construct a referenced gene-gene association network based on the protein-protein interaction networks. At last, we refine the spurious edges in the integrated gene functional similarity network with the help of the referenced gene-gene association network. Experiment results indicate that the refined gene functional similarity network (RGFSN) exhibits a scale-free, small world and modular architecture, with its degrees fit best to power law distribution. In addition, we conduct protein complex prediction experiment for human based on RGFSN and achieve an outstanding result, which implies it has high reliability and wide application significance. CONCLUSIONS:Our efforts are insightful for constructing and refining gene functional similarity networks, which can be applied to build other high quality biological networks.

SUBMITTER: Tian Z

PROVIDER: S-EPMC5751769 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

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Refine gene functional similarity network based on interaction networks.

Tian Zhen Z Guo Maozu M Wang Chunyu C Liu Xiaoyan X Wang Shiming S

BMC bioinformatics 20171228 Suppl 16

<h4>Background</h4>In recent years, biological interaction networks have become the basis of some essential study and achieved success in many applications. Some typical networks such as protein-protein interaction networks have already been investigated systematically. However, little work has been available for the construction of gene functional similarity networks so far. In this research, we will try to build a high reliable gene functional similarity network to promote its further applicat ...[more]

PMID: 29297381

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Project description:BackgroundStudies have shown that miRNAs are functionally associated with the development of many human diseases, but the roles of miRNAs in diseases and their underlying molecular mechanisms have not been fully understood. The research on miRNA-disease interaction has received more and more attention. Compared with the complexity and high cost of biological experiments, computational methods can rapidly and efficiently predict the potential miRNA-disease interaction and can be used as a beneficial supplement to experimental methods.ResultsIn this paper, we proposed a novel computational model of kernel neighborhood similarity and multi-network bidirectional propagation (KNMBP) for miRNA-disease interaction prediction, especially for new miRNAs and new diseases. First, we integrated multiple data sources of diseases and miRNAs, respectively, to construct a novel disease semantic similarity network and miRNA functional similarity network. Secondly, based on the modified miRNA-disease interactions, we use the kernel neighborhood similarity algorithm to calculate the disease kernel neighborhood similarity and the miRNA kernel neighborhood similarity. Finally, we utilize bidirectional propagation algorithm to predict the miRNA-disease interaction scores based on the integrated disease similarity network and miRNA similarity network. As a result, the AUC value of 5-fold cross validation for all interactions by KNMBP is 0.93126 based on the commonly used dataset, and the AUC values for all interactions, for all miRNAs, for all disease is 0.93795、0.86363、0.86937 based on another dataset extracted by ourselves, which are higher than other state-of-the-art methods. In addition, our model has good parameter robustness. The case study further demonstrated the predictive performance of the model for novel miRNA-disease interactions.ConclusionsOur KNMBP algorithm efficiently integrates multiple omics data from miRNAs and diseases to stably and efficiently predict potential miRNA-disease interactions. It is anticipated that KNMBP would be a useful tool in biomedical research.

Dataset Information

Refine gene functional similarity network based on interaction networks.

Publications

Refine gene functional similarity network based on interaction networks.

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