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A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules

BACKGROUND:  Gene co-expression network analysis (GCNA) is widely adopted in bioinformatics and biomedical research with applications such as gene function prediction, protein-protein interaction inference, disease markers identification, and copy number variance discovery. Currently there is a lack...

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Autores principales: Han, Zhi, Zhang, Jie, Sun, Guoyuan, Liu, Gang, Huang, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001231/
https://www.ncbi.nlm.nih.gov/pubmed/27556416
http://dx.doi.org/10.1186/s12864-016-2912-y
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author Han, Zhi
Zhang, Jie
Sun, Guoyuan
Liu, Gang
Huang, Kun
author_facet Han, Zhi
Zhang, Jie
Sun, Guoyuan
Liu, Gang
Huang, Kun
author_sort Han, Zhi
collection PubMed
description BACKGROUND:  Gene co-expression network analysis (GCNA) is widely adopted in bioinformatics and biomedical research with applications such as gene function prediction, protein-protein interaction inference, disease markers identification, and copy number variance discovery. Currently there is a lack of rigorous analysis on the mathematical condition for which the co-expressed gene module should satisfy. METHODS: In this paper, we present a linear algebraic based Centralized Concordance Index (CCI) for evaluating the concordance of co-expressed gene modules from gene co-expression network analysis. The CCI can be used to evaluate the performance for co-expression network analysis algorithms as well as for detecting condition specific co-expression modules. We applied CCI in detecting lung tumor specific gene modules. RESULTS AND DISCUSSION: Simulation showed that CCI is a robust indicator for evaluating the concordance of a group of co-expressed genes. The application to lung cancer datasets revealed interesting potential tumor specific genetic alterations including CNVs and even hints for gene-fusion. Deeper analysis required for understanding the molecular mechanisms of all such condition specific co-expression relationships. CONCLUSION: The CCI can be used to evaluate the performance for co-expression network analysis algorithms as well as for detecting condition specific co-expression modules. It is shown to be more robust to outliers and interfering modules than density based on Pearson correlation coefficients.
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spelling pubmed-50012312016-09-06 A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules Han, Zhi Zhang, Jie Sun, Guoyuan Liu, Gang Huang, Kun BMC Genomics Research BACKGROUND:  Gene co-expression network analysis (GCNA) is widely adopted in bioinformatics and biomedical research with applications such as gene function prediction, protein-protein interaction inference, disease markers identification, and copy number variance discovery. Currently there is a lack of rigorous analysis on the mathematical condition for which the co-expressed gene module should satisfy. METHODS: In this paper, we present a linear algebraic based Centralized Concordance Index (CCI) for evaluating the concordance of co-expressed gene modules from gene co-expression network analysis. The CCI can be used to evaluate the performance for co-expression network analysis algorithms as well as for detecting condition specific co-expression modules. We applied CCI in detecting lung tumor specific gene modules. RESULTS AND DISCUSSION: Simulation showed that CCI is a robust indicator for evaluating the concordance of a group of co-expressed genes. The application to lung cancer datasets revealed interesting potential tumor specific genetic alterations including CNVs and even hints for gene-fusion. Deeper analysis required for understanding the molecular mechanisms of all such condition specific co-expression relationships. CONCLUSION: The CCI can be used to evaluate the performance for co-expression network analysis algorithms as well as for detecting condition specific co-expression modules. It is shown to be more robust to outliers and interfering modules than density based on Pearson correlation coefficients. BioMed Central 2016-08-22 /pmc/articles/PMC5001231/ /pubmed/27556416 http://dx.doi.org/10.1186/s12864-016-2912-y Text en © The Author(s). 2016 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
Han, Zhi
Zhang, Jie
Sun, Guoyuan
Liu, Gang
Huang, Kun
A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules
title A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules
title_full A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules
title_fullStr A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules
title_full_unstemmed A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules
title_short A matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules
title_sort matrix rank based concordance index for evaluating and detecting conditional specific co-expressed gene modules
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001231/
https://www.ncbi.nlm.nih.gov/pubmed/27556416
http://dx.doi.org/10.1186/s12864-016-2912-y
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