File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Functional module analysis for gene coexpression networks with network integration

TitleFunctional module analysis for gene coexpression networks with network integration
Authors
Keywordsgene coexpression networks
spectral clustering
Functional module identification
network integration
Issue Date2015
Citation
IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2015, v. 12, n. 5, p. 1146-1160 How to Cite?
Abstract© 2015 IEEE. Network has been a general tool for studying the complex interactions between different genes, proteins, and other small molecules. Module as a fundamental property of many biological networks has been widely studied and many computational methods have been proposed to identify the modules in an individual network. However, in many cases, a single network is insufficient for module analysis due to the noise in the data or the tuning of parameters when building the biological network. The availability of a large amount of biological networks makes network integration study possible. By integrating such networks, more informative modules for some specific disease can be derived from the networks constructed from different tissues, and consistent factors for different diseases can be inferred. In this paper, we have developed an effective method for module identification from multiple networks under different conditions. The problem is formulated as an optimization model, which combines the module identification in each individual network and alignment of the modules from different networks together. An approximation algorithm based on eigenvector computation is proposed. Our method outperforms the existing methods, especially when the underlying modules in multiple networks are different in simulation studies. We also applied our method to two groups of gene coexpression networks for humans, which include one for three different cancers, and one for three tissues from the morbidly obese patients. We identified 13 modules with three complete subgraphs, and 11 modules with two complete subgraphs, respectively. The modules were validated through Gene Ontology enrichment and KEGG pathway enrichment analysis. We also showed that the main functions of most modules for the corresponding disease have been addressed by other researchers, which may provide the theoretical basis for further studying the modules experimentally.
Persistent Identifierhttp://hdl.handle.net/10722/276706
ISSN
2021 Impact Factor: 3.702
2020 SCImago Journal Rankings: 0.745
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhang, Shuqin-
dc.contributor.authorZhao, Hongyu-
dc.contributor.authorNg, Michael K.-
dc.date.accessioned2019-09-18T08:34:24Z-
dc.date.available2019-09-18T08:34:24Z-
dc.date.issued2015-
dc.identifier.citationIEEE/ACM Transactions on Computational Biology and Bioinformatics, 2015, v. 12, n. 5, p. 1146-1160-
dc.identifier.issn1545-5963-
dc.identifier.urihttp://hdl.handle.net/10722/276706-
dc.description.abstract© 2015 IEEE. Network has been a general tool for studying the complex interactions between different genes, proteins, and other small molecules. Module as a fundamental property of many biological networks has been widely studied and many computational methods have been proposed to identify the modules in an individual network. However, in many cases, a single network is insufficient for module analysis due to the noise in the data or the tuning of parameters when building the biological network. The availability of a large amount of biological networks makes network integration study possible. By integrating such networks, more informative modules for some specific disease can be derived from the networks constructed from different tissues, and consistent factors for different diseases can be inferred. In this paper, we have developed an effective method for module identification from multiple networks under different conditions. The problem is formulated as an optimization model, which combines the module identification in each individual network and alignment of the modules from different networks together. An approximation algorithm based on eigenvector computation is proposed. Our method outperforms the existing methods, especially when the underlying modules in multiple networks are different in simulation studies. We also applied our method to two groups of gene coexpression networks for humans, which include one for three different cancers, and one for three tissues from the morbidly obese patients. We identified 13 modules with three complete subgraphs, and 11 modules with two complete subgraphs, respectively. The modules were validated through Gene Ontology enrichment and KEGG pathway enrichment analysis. We also showed that the main functions of most modules for the corresponding disease have been addressed by other researchers, which may provide the theoretical basis for further studying the modules experimentally.-
dc.languageeng-
dc.relation.ispartofIEEE/ACM Transactions on Computational Biology and Bioinformatics-
dc.subjectgene coexpression networks-
dc.subjectspectral clustering-
dc.subjectFunctional module identification-
dc.subjectnetwork integration-
dc.titleFunctional module analysis for gene coexpression networks with network integration-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1109/TCBB.2015.2396073-
dc.identifier.pmid26451826-
dc.identifier.scopuseid_2-s2.0-84951913497-
dc.identifier.volume12-
dc.identifier.issue5-
dc.identifier.spage1146-
dc.identifier.epage1160-
dc.identifier.isiWOS:000362909500017-
dc.identifier.issnl1545-5963-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats