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Semantic integration to identify overlapping functional modules in protein interaction networks
BACKGROUND: The systematic analysis of protein-protein interactions can enable a better understanding of cellular organization, processes and functions. Functional modules can be identified from the protein interaction networks derived from experimental data sets. However, these analyses are challen...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971074/ https://www.ncbi.nlm.nih.gov/pubmed/17650343 http://dx.doi.org/10.1186/1471-2105-8-265 |
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author | Cho, Young-Rae Hwang, Woochang Ramanathan, Murali Zhang, Aidong |
author_facet | Cho, Young-Rae Hwang, Woochang Ramanathan, Murali Zhang, Aidong |
author_sort | Cho, Young-Rae |
collection | PubMed |
description | BACKGROUND: The systematic analysis of protein-protein interactions can enable a better understanding of cellular organization, processes and functions. Functional modules can be identified from the protein interaction networks derived from experimental data sets. However, these analyses are challenging because of the presence of unreliable interactions and the complex connectivity of the network. The integration of protein-protein interactions with the data from other sources can be leveraged for improving the effectiveness of functional module detection algorithms. RESULTS: We have developed novel metrics, called semantic similarity and semantic interactivity, which use Gene Ontology (GO) annotations to measure the reliability of protein-protein interactions. The protein interaction networks can be converted into a weighted graph representation by assigning the reliability values to each interaction as a weight. We presented a flow-based modularization algorithm to efficiently identify overlapping modules in the weighted interaction networks. The experimental results show that the semantic similarity and semantic interactivity of interacting pairs were positively correlated with functional co-occurrence. The effectiveness of the algorithm for identifying modules was evaluated using functional categories from the MIPS database. We demonstrated that our algorithm had higher accuracy compared to other competing approaches. CONCLUSION: The integration of protein interaction networks with GO annotation data and the capability of detecting overlapping modules substantially improve the accuracy of module identification. |
format | Text |
id | pubmed-1971074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-19710742007-09-07 Semantic integration to identify overlapping functional modules in protein interaction networks Cho, Young-Rae Hwang, Woochang Ramanathan, Murali Zhang, Aidong BMC Bioinformatics Methodology Article BACKGROUND: The systematic analysis of protein-protein interactions can enable a better understanding of cellular organization, processes and functions. Functional modules can be identified from the protein interaction networks derived from experimental data sets. However, these analyses are challenging because of the presence of unreliable interactions and the complex connectivity of the network. The integration of protein-protein interactions with the data from other sources can be leveraged for improving the effectiveness of functional module detection algorithms. RESULTS: We have developed novel metrics, called semantic similarity and semantic interactivity, which use Gene Ontology (GO) annotations to measure the reliability of protein-protein interactions. The protein interaction networks can be converted into a weighted graph representation by assigning the reliability values to each interaction as a weight. We presented a flow-based modularization algorithm to efficiently identify overlapping modules in the weighted interaction networks. The experimental results show that the semantic similarity and semantic interactivity of interacting pairs were positively correlated with functional co-occurrence. The effectiveness of the algorithm for identifying modules was evaluated using functional categories from the MIPS database. We demonstrated that our algorithm had higher accuracy compared to other competing approaches. CONCLUSION: The integration of protein interaction networks with GO annotation data and the capability of detecting overlapping modules substantially improve the accuracy of module identification. BioMed Central 2007-07-24 /pmc/articles/PMC1971074/ /pubmed/17650343 http://dx.doi.org/10.1186/1471-2105-8-265 Text en Copyright © 2007 Cho et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Cho, Young-Rae Hwang, Woochang Ramanathan, Murali Zhang, Aidong Semantic integration to identify overlapping functional modules in protein interaction networks |
title | Semantic integration to identify overlapping functional modules in protein interaction networks |
title_full | Semantic integration to identify overlapping functional modules in protein interaction networks |
title_fullStr | Semantic integration to identify overlapping functional modules in protein interaction networks |
title_full_unstemmed | Semantic integration to identify overlapping functional modules in protein interaction networks |
title_short | Semantic integration to identify overlapping functional modules in protein interaction networks |
title_sort | semantic integration to identify overlapping functional modules in protein interaction networks |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971074/ https://www.ncbi.nlm.nih.gov/pubmed/17650343 http://dx.doi.org/10.1186/1471-2105-8-265 |
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