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iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks

BACKGROUND: The speed at which biological datasets are being accumulated stands in contrast to our ability to integrate them meaningfully. Large-scale biological databases containing datasets of genes, proteins, cells, organs, and diseases are being created but they are not connected. Integration of...

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Autores principales: Wang, Lili, Khankhanian, Pouya, Baranzini, Sergio E, Mousavi, Parvin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190406/
https://www.ncbi.nlm.nih.gov/pubmed/21943367
http://dx.doi.org/10.1186/1471-2105-12-380
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author Wang, Lili
Khankhanian, Pouya
Baranzini, Sergio E
Mousavi, Parvin
author_facet Wang, Lili
Khankhanian, Pouya
Baranzini, Sergio E
Mousavi, Parvin
author_sort Wang, Lili
collection PubMed
description BACKGROUND: The speed at which biological datasets are being accumulated stands in contrast to our ability to integrate them meaningfully. Large-scale biological databases containing datasets of genes, proteins, cells, organs, and diseases are being created but they are not connected. Integration of these vast but heterogeneous sources of information will allow the systematic and comprehensive analysis of molecular and clinical datasets, spanning hundreds of dimensions and thousands of individuals. This integration is essential to capitalize on the value of current and future molecular- and cellular-level data on humans to gain novel insights about health and disease. RESULTS: We describe a new open-source Cytoscape plugin named iCTNet (integrated Complex Traits Networks). iCTNet integrates several data sources to allow automated and systematic creation of networks with up to five layers of omics information: phenotype-SNP association, protein-protein interaction, disease-tissue, tissue-gene, and drug-gene relationships. It facilitates the generation of general or specific network views with diverse options for more than 200 diseases. Built-in tools are provided to prioritize candidate genes and create modules of specific phenotypes. CONCLUSIONS: iCTNet provides a user-friendly interface to search, integrate, visualize, and analyze genome-scale biological networks for human complex traits. We argue this tool is a key instrument that facilitates systematic integration of disparate large-scale data through network visualization, ultimately allowing the identification of disease similarities and the design of novel therapeutic approaches. The online database and Cytoscape plugin are freely available for academic use at: http://www.cs.queensu.ca/ictnet
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spelling pubmed-31904062011-10-12 iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks Wang, Lili Khankhanian, Pouya Baranzini, Sergio E Mousavi, Parvin BMC Bioinformatics Software BACKGROUND: The speed at which biological datasets are being accumulated stands in contrast to our ability to integrate them meaningfully. Large-scale biological databases containing datasets of genes, proteins, cells, organs, and diseases are being created but they are not connected. Integration of these vast but heterogeneous sources of information will allow the systematic and comprehensive analysis of molecular and clinical datasets, spanning hundreds of dimensions and thousands of individuals. This integration is essential to capitalize on the value of current and future molecular- and cellular-level data on humans to gain novel insights about health and disease. RESULTS: We describe a new open-source Cytoscape plugin named iCTNet (integrated Complex Traits Networks). iCTNet integrates several data sources to allow automated and systematic creation of networks with up to five layers of omics information: phenotype-SNP association, protein-protein interaction, disease-tissue, tissue-gene, and drug-gene relationships. It facilitates the generation of general or specific network views with diverse options for more than 200 diseases. Built-in tools are provided to prioritize candidate genes and create modules of specific phenotypes. CONCLUSIONS: iCTNet provides a user-friendly interface to search, integrate, visualize, and analyze genome-scale biological networks for human complex traits. We argue this tool is a key instrument that facilitates systematic integration of disparate large-scale data through network visualization, ultimately allowing the identification of disease similarities and the design of novel therapeutic approaches. The online database and Cytoscape plugin are freely available for academic use at: http://www.cs.queensu.ca/ictnet BioMed Central 2011-09-26 /pmc/articles/PMC3190406/ /pubmed/21943367 http://dx.doi.org/10.1186/1471-2105-12-380 Text en Copyright © 2011 Wang et al; licensee BioMed Central Ltd. https://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 (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software
Wang, Lili
Khankhanian, Pouya
Baranzini, Sergio E
Mousavi, Parvin
iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks
title iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks
title_full iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks
title_fullStr iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks
title_full_unstemmed iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks
title_short iCTNet: A Cytoscape plugin to produce and analyze integrative complex traits networks
title_sort ictnet: a cytoscape plugin to produce and analyze integrative complex traits networks
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190406/
https://www.ncbi.nlm.nih.gov/pubmed/21943367
http://dx.doi.org/10.1186/1471-2105-12-380
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