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The integration of weighted human gene association networks based on link prediction

BACKGROUND: Physical and functional interplays between genes or proteins have important biological meaning for cellular functions. Some efforts have been made to construct weighted gene association meta-networks by integrating multiple biological resources, where the weight indicates the confidence...

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Autores principales: Yang, Jian, Yang, Tinghong, Wu, Duzhi, Lin, Limei, Yang, Fan, Zhao, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282786/
https://www.ncbi.nlm.nih.gov/pubmed/28137253
http://dx.doi.org/10.1186/s12918-017-0398-0
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author Yang, Jian
Yang, Tinghong
Wu, Duzhi
Lin, Limei
Yang, Fan
Zhao, Jing
author_facet Yang, Jian
Yang, Tinghong
Wu, Duzhi
Lin, Limei
Yang, Fan
Zhao, Jing
author_sort Yang, Jian
collection PubMed
description BACKGROUND: Physical and functional interplays between genes or proteins have important biological meaning for cellular functions. Some efforts have been made to construct weighted gene association meta-networks by integrating multiple biological resources, where the weight indicates the confidence of the interaction. However, it is found that these existing human gene association networks share only quite limited overlapped interactions, suggesting their incompleteness and noise. RESULTS: Here we proposed a workflow to construct a weighted human gene association network using information of six existing networks, including two weighted specific PPI networks and four gene association meta-networks. We applied link prediction algorithm to predict possible missing links of the networks, cross-validation approach to refine each network and finally integrated the refined networks to get the final integrated network. CONCLUSIONS: The common information among the refined networks increases notably, suggesting their higher reliability. Our final integrated network owns much more links than most of the original networks, meanwhile its links still keep high functional relevance. Being used as background network in a case study of disease gene prediction, the final integrated network presents good performance, implying its reliability and application significance. Our workflow could be insightful for integrating and refining existing gene association data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-017-0398-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-52827862017-02-03 The integration of weighted human gene association networks based on link prediction Yang, Jian Yang, Tinghong Wu, Duzhi Lin, Limei Yang, Fan Zhao, Jing BMC Syst Biol Research Article BACKGROUND: Physical and functional interplays between genes or proteins have important biological meaning for cellular functions. Some efforts have been made to construct weighted gene association meta-networks by integrating multiple biological resources, where the weight indicates the confidence of the interaction. However, it is found that these existing human gene association networks share only quite limited overlapped interactions, suggesting their incompleteness and noise. RESULTS: Here we proposed a workflow to construct a weighted human gene association network using information of six existing networks, including two weighted specific PPI networks and four gene association meta-networks. We applied link prediction algorithm to predict possible missing links of the networks, cross-validation approach to refine each network and finally integrated the refined networks to get the final integrated network. CONCLUSIONS: The common information among the refined networks increases notably, suggesting their higher reliability. Our final integrated network owns much more links than most of the original networks, meanwhile its links still keep high functional relevance. Being used as background network in a case study of disease gene prediction, the final integrated network presents good performance, implying its reliability and application significance. Our workflow could be insightful for integrating and refining existing gene association data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-017-0398-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-31 /pmc/articles/PMC5282786/ /pubmed/28137253 http://dx.doi.org/10.1186/s12918-017-0398-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yang, Jian
Yang, Tinghong
Wu, Duzhi
Lin, Limei
Yang, Fan
Zhao, Jing
The integration of weighted human gene association networks based on link prediction
title The integration of weighted human gene association networks based on link prediction
title_full The integration of weighted human gene association networks based on link prediction
title_fullStr The integration of weighted human gene association networks based on link prediction
title_full_unstemmed The integration of weighted human gene association networks based on link prediction
title_short The integration of weighted human gene association networks based on link prediction
title_sort integration of weighted human gene association networks based on link prediction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282786/
https://www.ncbi.nlm.nih.gov/pubmed/28137253
http://dx.doi.org/10.1186/s12918-017-0398-0
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