Please use this identifier to cite or link to this item: https://doi.org/10.1186/1752-0509-2-93
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dc.titleAn in silico method for detecting overlapping functional modules from composite biological networks
dc.contributor.authorMaraziotis, I.A
dc.contributor.authorDimitrakopoulou, K
dc.contributor.authorBezerianos, A
dc.date.accessioned2020-10-20T08:27:06Z
dc.date.available2020-10-20T08:27:06Z
dc.date.issued2008
dc.identifier.citationMaraziotis, I.A, Dimitrakopoulou, K, Bezerianos, A (2008). An in silico method for detecting overlapping functional modules from composite biological networks. BMC Systems Biology 2 : 93. ScholarBank@NUS Repository. https://doi.org/10.1186/1752-0509-2-93
dc.identifier.issn1752-0509
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178231
dc.description.abstractBackground: The ever-increasing flow of gene expression and protein-protein interaction (PPI) data has assisted in understanding the dynamics of the cell. The detection of functional modules is the first step in deciphering the apparent modularity of biological networks. However, most network-partitioning algorithms consider only the topological aspects and ignore the underlying functional relationships. Results: In the current study we integrate proteomics and microarray data of yeast, in the form of a weighted PPI graph. We partition the enriched PPI network with the novel DetMod algorithm and we identify 335 modules. One of the main advantages of DetMod is that it manages to capture the inter-module cross-talk by allowing a controlled degree of overlap among the detected modules. The obtained modules are densely connected in terms of protein interactions, while their members share up to a high degree similar biological process GO terms. Moreover, known protein complexes are largely incorporated in the assessed modules. Finally, we display the prevalence of our method against modules resulting from other computational approaches. Conclusion: The successful integration of heterogeneous data and the concept of the proposed algorithm provide confident functional modules. We also proved that our approach is superior to methods restricted to PPI data only. © 2008 Maraziotis et al; licensee BioMed Central Ltd.
dc.publisherBMC
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectalgorithm
dc.subjectarticle
dc.subjectbiology
dc.subjectDNA microarray
dc.subjectgene expression profiling
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectprotein binding
dc.subjectproteomics
dc.subjectreproducibility
dc.subjectSaccharomyces cerevisiae
dc.subjectAlgorithms
dc.subjectComputational Biology
dc.subjectGene Expression Profiling
dc.subjectOligonucleotide Array Sequence Analysis
dc.subjectProtein Binding
dc.subjectProteomics
dc.subjectReproducibility of Results
dc.subjectSaccharomyces cerevisiae
dc.typeArticle
dc.contributor.departmentLIFE SCIENCES INSTITUTE
dc.description.doi10.1186/1752-0509-2-93
dc.description.sourcetitleBMC Systems Biology
dc.description.volume2
dc.description.page93
dc.published.statepublished
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