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LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network
BACKGROUND: Cancer is a complex disease which is characterized by the accumulation of genetic alterations during the patient’s lifetime. With the development of the next-generation sequencing technology, multiple omics data, such as cancer genomic, epigenomic and transcriptomic data etc., can be mea...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259866/ https://www.ncbi.nlm.nih.gov/pubmed/28155630 http://dx.doi.org/10.1186/s12859-016-1332-y |
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author | Wei, Pi-Jing Zhang, Di Xia, Junfeng Zheng, Chun-Hou |
author_facet | Wei, Pi-Jing Zhang, Di Xia, Junfeng Zheng, Chun-Hou |
author_sort | Wei, Pi-Jing |
collection | PubMed |
description | BACKGROUND: Cancer is a complex disease which is characterized by the accumulation of genetic alterations during the patient’s lifetime. With the development of the next-generation sequencing technology, multiple omics data, such as cancer genomic, epigenomic and transcriptomic data etc., can be measured from each individual. Correspondingly, one of the key challenges is to pinpoint functional driver mutations or pathways, which contributes to tumorigenesis, from millions of functional neutral passenger mutations. RESULTS: In this paper, in order to identify driver genes effectively, we applied a generalized additive model to mutation profiles to filter genes with long length and constructed a new gene-gene interaction network. Then we integrated the mutation data and expression data into the gene-gene interaction network. Lastly, greedy algorithm was used to prioritize candidate driver genes from the integrated data. We named the proposed method Length-Net-Driver (LNDriver). CONCLUSIONS: Experiments on three TCGA datasets, i.e., head and neck squamous cell carcinoma, kidney renal clear cell carcinoma and thyroid carcinoma, demonstrated that the proposed method was effective. Also, it can identify not only frequently mutated drivers, but also rare candidate driver genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1332-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5259866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52598662017-01-26 LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network Wei, Pi-Jing Zhang, Di Xia, Junfeng Zheng, Chun-Hou BMC Bioinformatics Research BACKGROUND: Cancer is a complex disease which is characterized by the accumulation of genetic alterations during the patient’s lifetime. With the development of the next-generation sequencing technology, multiple omics data, such as cancer genomic, epigenomic and transcriptomic data etc., can be measured from each individual. Correspondingly, one of the key challenges is to pinpoint functional driver mutations or pathways, which contributes to tumorigenesis, from millions of functional neutral passenger mutations. RESULTS: In this paper, in order to identify driver genes effectively, we applied a generalized additive model to mutation profiles to filter genes with long length and constructed a new gene-gene interaction network. Then we integrated the mutation data and expression data into the gene-gene interaction network. Lastly, greedy algorithm was used to prioritize candidate driver genes from the integrated data. We named the proposed method Length-Net-Driver (LNDriver). CONCLUSIONS: Experiments on three TCGA datasets, i.e., head and neck squamous cell carcinoma, kidney renal clear cell carcinoma and thyroid carcinoma, demonstrated that the proposed method was effective. Also, it can identify not only frequently mutated drivers, but also rare candidate driver genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1332-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-23 /pmc/articles/PMC5259866/ /pubmed/28155630 http://dx.doi.org/10.1186/s12859-016-1332-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 Wei, Pi-Jing Zhang, Di Xia, Junfeng Zheng, Chun-Hou LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network |
title | LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network |
title_full | LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network |
title_fullStr | LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network |
title_full_unstemmed | LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network |
title_short | LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network |
title_sort | lndriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259866/ https://www.ncbi.nlm.nih.gov/pubmed/28155630 http://dx.doi.org/10.1186/s12859-016-1332-y |
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