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Detection of divergent genes in microbial aCGH experiments

BACKGROUND: Array-based comparative genome hybridization (aCGH) is a tool for rapid comparison of genomes from different bacterial strains. The purpose of such analysis is to detect highly divergent or absent genes in a sample strain compared to an index strain. Development of methods for analyzing...

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Autores principales: Snipen, Lars, Repsilber, Dirk, Nyquist, Ludvig, Ziegler, Andreas, Aakra, Ågot, Aastveit, Are
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563484/
https://www.ncbi.nlm.nih.gov/pubmed/16573812
http://dx.doi.org/10.1186/1471-2105-7-181
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author Snipen, Lars
Repsilber, Dirk
Nyquist, Ludvig
Ziegler, Andreas
Aakra, Ågot
Aastveit, Are
author_facet Snipen, Lars
Repsilber, Dirk
Nyquist, Ludvig
Ziegler, Andreas
Aakra, Ågot
Aastveit, Are
author_sort Snipen, Lars
collection PubMed
description BACKGROUND: Array-based comparative genome hybridization (aCGH) is a tool for rapid comparison of genomes from different bacterial strains. The purpose of such analysis is to detect highly divergent or absent genes in a sample strain compared to an index strain. Development of methods for analyzing aCGH data has primarily focused on copy number abberations in cancer research. In microbial aCGH analyses, genes are typically ranked by log-ratios, and classification into divergent or present is done by choosing a cutoff log-ratio, either manually or by statistics calculated from the log-ratio distribution. As experimental settings vary considerably, it is not possible to develop a classical discriminant or statistical learning approach. METHODS: We introduce a more efficient method for analyzing microbial aCGH data using a finite mixture model and a data rotation scheme. Using the average posterior probabilities from the model fitted to log-ratios before and after rotation, we get a score for each gene, and demonstrate its advantages for ranking and detecting divergent genes with enlarged specificity and sensitivity. RESULTS: The procedure is tested and compared to other approaches on simulated data sets, as well as on four experimental validation data sets for aCGH analysis on fully sequenced strains of Staphylococcus aureus and Streptococcus pneumoniae. CONCLUSION: When tested on simulated data as well as on four different experimental validation data sets from experiments with only fully sequenced strains, our procedure out-competes the standard procedures of using a simple log-ratio cutoff for classification into present and divergent genes.
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spelling pubmed-15634842006-09-11 Detection of divergent genes in microbial aCGH experiments Snipen, Lars Repsilber, Dirk Nyquist, Ludvig Ziegler, Andreas Aakra, Ågot Aastveit, Are BMC Bioinformatics Research Article BACKGROUND: Array-based comparative genome hybridization (aCGH) is a tool for rapid comparison of genomes from different bacterial strains. The purpose of such analysis is to detect highly divergent or absent genes in a sample strain compared to an index strain. Development of methods for analyzing aCGH data has primarily focused on copy number abberations in cancer research. In microbial aCGH analyses, genes are typically ranked by log-ratios, and classification into divergent or present is done by choosing a cutoff log-ratio, either manually or by statistics calculated from the log-ratio distribution. As experimental settings vary considerably, it is not possible to develop a classical discriminant or statistical learning approach. METHODS: We introduce a more efficient method for analyzing microbial aCGH data using a finite mixture model and a data rotation scheme. Using the average posterior probabilities from the model fitted to log-ratios before and after rotation, we get a score for each gene, and demonstrate its advantages for ranking and detecting divergent genes with enlarged specificity and sensitivity. RESULTS: The procedure is tested and compared to other approaches on simulated data sets, as well as on four experimental validation data sets for aCGH analysis on fully sequenced strains of Staphylococcus aureus and Streptococcus pneumoniae. CONCLUSION: When tested on simulated data as well as on four different experimental validation data sets from experiments with only fully sequenced strains, our procedure out-competes the standard procedures of using a simple log-ratio cutoff for classification into present and divergent genes. BioMed Central 2006-03-30 /pmc/articles/PMC1563484/ /pubmed/16573812 http://dx.doi.org/10.1186/1471-2105-7-181 Text en Copyright © 2006 Snipen et al; licensee BioMed Central Ltd. https://creativecommons.org/licenses/by/2.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Snipen, Lars
Repsilber, Dirk
Nyquist, Ludvig
Ziegler, Andreas
Aakra, Ågot
Aastveit, Are
Detection of divergent genes in microbial aCGH experiments
title Detection of divergent genes in microbial aCGH experiments
title_full Detection of divergent genes in microbial aCGH experiments
title_fullStr Detection of divergent genes in microbial aCGH experiments
title_full_unstemmed Detection of divergent genes in microbial aCGH experiments
title_short Detection of divergent genes in microbial aCGH experiments
title_sort detection of divergent genes in microbial acgh experiments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563484/
https://www.ncbi.nlm.nih.gov/pubmed/16573812
http://dx.doi.org/10.1186/1471-2105-7-181
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