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Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data
MOTIVATION: Growth phenotype profiling of genome-wide gene-deletion strains over stress conditions can offer a clear picture that the essentiality of genes depends on environmental conditions. Systematically identifying groups of genes from such high-throughput data that share similar patterns of co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870648/ https://www.ncbi.nlm.nih.gov/pubmed/28379298 http://dx.doi.org/10.1093/bioinformatics/btx199 |
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author | Alzahrani, Majed Kuwahara, Hiroyuki Wang, Wei Gao, Xin |
author_facet | Alzahrani, Majed Kuwahara, Hiroyuki Wang, Wei Gao, Xin |
author_sort | Alzahrani, Majed |
collection | PubMed |
description | MOTIVATION: Growth phenotype profiling of genome-wide gene-deletion strains over stress conditions can offer a clear picture that the essentiality of genes depends on environmental conditions. Systematically identifying groups of genes from such high-throughput data that share similar patterns of conditional essentiality and dispensability under various environmental conditions can elucidate how genetic interactions of the growth phenotype are regulated in response to the environment. RESULTS: We first demonstrate that detecting such ‘co-fit’ gene groups can be cast as a less well-studied problem in biclustering, i.e. constant-column biclustering. Despite significant advances in biclustering techniques, very few were designed for mining in growth phenotype data. Here, we propose Gracob, a novel, efficient graph-based method that casts and solves the constant-column biclustering problem as a maximal clique finding problem in a multipartite graph. We compared Gracob with a large collection of widely used biclustering methods that cover different types of algorithms designed to detect different types of biclusters. Gracob showed superior performance on finding co-fit genes over all the existing methods on both a variety of synthetic data sets with a wide range of settings, and three real growth phenotype datasets for E. coli, proteobacteria and yeast. AVAILABILITY AND IMPLEMENTATION: Our program is freely available for download at http://sfb.kaust.edu.sa/Pages/Software.aspx. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-5870648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58706482018-04-05 Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data Alzahrani, Majed Kuwahara, Hiroyuki Wang, Wei Gao, Xin Bioinformatics Original Papers MOTIVATION: Growth phenotype profiling of genome-wide gene-deletion strains over stress conditions can offer a clear picture that the essentiality of genes depends on environmental conditions. Systematically identifying groups of genes from such high-throughput data that share similar patterns of conditional essentiality and dispensability under various environmental conditions can elucidate how genetic interactions of the growth phenotype are regulated in response to the environment. RESULTS: We first demonstrate that detecting such ‘co-fit’ gene groups can be cast as a less well-studied problem in biclustering, i.e. constant-column biclustering. Despite significant advances in biclustering techniques, very few were designed for mining in growth phenotype data. Here, we propose Gracob, a novel, efficient graph-based method that casts and solves the constant-column biclustering problem as a maximal clique finding problem in a multipartite graph. We compared Gracob with a large collection of widely used biclustering methods that cover different types of algorithms designed to detect different types of biclusters. Gracob showed superior performance on finding co-fit genes over all the existing methods on both a variety of synthetic data sets with a wide range of settings, and three real growth phenotype datasets for E. coli, proteobacteria and yeast. AVAILABILITY AND IMPLEMENTATION: Our program is freely available for download at http://sfb.kaust.edu.sa/Pages/Software.aspx. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2017-08-15 2017-04-04 /pmc/articles/PMC5870648/ /pubmed/28379298 http://dx.doi.org/10.1093/bioinformatics/btx199 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Papers Alzahrani, Majed Kuwahara, Hiroyuki Wang, Wei Gao, Xin Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data |
title | Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data |
title_full | Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data |
title_fullStr | Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data |
title_full_unstemmed | Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data |
title_short | Gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data |
title_sort | gracob: a novel graph-based constant-column biclustering method for mining growth phenotype data |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870648/ https://www.ncbi.nlm.nih.gov/pubmed/28379298 http://dx.doi.org/10.1093/bioinformatics/btx199 |
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