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Microbial genotype–phenotype mapping by class association rule mining

Motivation: Microbial phenotypes are typically due to the concerted action of multiple gene functions, yet the presence of each gene may have only a weak correlation with the observed phenotype. Hence, it may be more appropriate to examine co-occurrence between sets of genes and a phenotype (multipl...

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Autores principales: Tamura, Makio, D'haeseleer, Patrik
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2718668/
https://www.ncbi.nlm.nih.gov/pubmed/18467347
http://dx.doi.org/10.1093/bioinformatics/btn210
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author Tamura, Makio
D'haeseleer, Patrik
author_facet Tamura, Makio
D'haeseleer, Patrik
author_sort Tamura, Makio
collection PubMed
description Motivation: Microbial phenotypes are typically due to the concerted action of multiple gene functions, yet the presence of each gene may have only a weak correlation with the observed phenotype. Hence, it may be more appropriate to examine co-occurrence between sets of genes and a phenotype (multiple-to-one) instead of pairwise relations between a single gene and the phenotype. Here, we propose an efficient class association rule mining algorithm, netCAR, in order to extract sets of COGs (clusters of orthologous groups of proteins) associated with a phenotype from COG phylogenetic profiles and a phenotype profile. netCAR takes into account the phylogenetic co-occurrence graph between COGs to restrict hypothesis space, and uses mutual information to evaluate the biconditional relation. Results: We examined the mining capability of pairwise and multiple-to-one association by using netCAR to extract COGs relevant to six microbial phenotypes (aerobic, anaerobic, facultative, endospore, motility and Gram negative) from 11 969 unique COG profiles across 155 prokaryotic organisms. With the same level of false discovery rate, multiple-to-one association can extract about 10 times more relevant COGs than one-to-one association. We also reveal various topologies of association networks among COGs (modules) from extracted multiple-to-one correlation rules relevant with the six phenotypes; including a well-connected network for motility, a star-shaped network for aerobic and intermediate topologies for the other phenotypes. netCAR outperforms a standard CAR mining algorithm, CARapriori, while requiring several orders of magnitude less computational time for extracting 3-COG sets. Availability: Source code of the Java implementation is available as Supplementary Material at the Bioinformatics online website, or upon request to the author. Contact: makio323@gmail.com Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-27186682009-07-31 Microbial genotype–phenotype mapping by class association rule mining Tamura, Makio D'haeseleer, Patrik Bioinformatics Original Papers Motivation: Microbial phenotypes are typically due to the concerted action of multiple gene functions, yet the presence of each gene may have only a weak correlation with the observed phenotype. Hence, it may be more appropriate to examine co-occurrence between sets of genes and a phenotype (multiple-to-one) instead of pairwise relations between a single gene and the phenotype. Here, we propose an efficient class association rule mining algorithm, netCAR, in order to extract sets of COGs (clusters of orthologous groups of proteins) associated with a phenotype from COG phylogenetic profiles and a phenotype profile. netCAR takes into account the phylogenetic co-occurrence graph between COGs to restrict hypothesis space, and uses mutual information to evaluate the biconditional relation. Results: We examined the mining capability of pairwise and multiple-to-one association by using netCAR to extract COGs relevant to six microbial phenotypes (aerobic, anaerobic, facultative, endospore, motility and Gram negative) from 11 969 unique COG profiles across 155 prokaryotic organisms. With the same level of false discovery rate, multiple-to-one association can extract about 10 times more relevant COGs than one-to-one association. We also reveal various topologies of association networks among COGs (modules) from extracted multiple-to-one correlation rules relevant with the six phenotypes; including a well-connected network for motility, a star-shaped network for aerobic and intermediate topologies for the other phenotypes. netCAR outperforms a standard CAR mining algorithm, CARapriori, while requiring several orders of magnitude less computational time for extracting 3-COG sets. Availability: Source code of the Java implementation is available as Supplementary Material at the Bioinformatics online website, or upon request to the author. Contact: makio323@gmail.com Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2008-07-01 2008-05-08 /pmc/articles/PMC2718668/ /pubmed/18467347 http://dx.doi.org/10.1093/bioinformatics/btn210 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Tamura, Makio
D'haeseleer, Patrik
Microbial genotype–phenotype mapping by class association rule mining
title Microbial genotype–phenotype mapping by class association rule mining
title_full Microbial genotype–phenotype mapping by class association rule mining
title_fullStr Microbial genotype–phenotype mapping by class association rule mining
title_full_unstemmed Microbial genotype–phenotype mapping by class association rule mining
title_short Microbial genotype–phenotype mapping by class association rule mining
title_sort microbial genotype–phenotype mapping by class association rule mining
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2718668/
https://www.ncbi.nlm.nih.gov/pubmed/18467347
http://dx.doi.org/10.1093/bioinformatics/btn210
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