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MycoBASE: expanding the functional annotation coverage of mycobacterial genomes

BACKGROUND: Central to most omic scale experiments is the interpretation and examination of resulting gene lists corresponding to differentially expressed, regulated, or observed gene or protein sets. Complicating interpretation is a lack of functional annotation assigned to a large percentage of ma...

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Autores principales: Garcia, Benjamin J., Datta, Gargi, Davidson, Rebecca M., Strong, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690229/
https://www.ncbi.nlm.nih.gov/pubmed/26704706
http://dx.doi.org/10.1186/s12864-015-2311-9
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author Garcia, Benjamin J.
Datta, Gargi
Davidson, Rebecca M.
Strong, Michael
author_facet Garcia, Benjamin J.
Datta, Gargi
Davidson, Rebecca M.
Strong, Michael
author_sort Garcia, Benjamin J.
collection PubMed
description BACKGROUND: Central to most omic scale experiments is the interpretation and examination of resulting gene lists corresponding to differentially expressed, regulated, or observed gene or protein sets. Complicating interpretation is a lack of functional annotation assigned to a large percentage of many microbial genomes. This is particularly noticeable in mycobacterial genomes, which are significantly divergent from many of the microbial model species used for gene and protein functional characterization, but which are extremely important clinically. Mycobacterial species, ranging from M. tuberculosis to M. abscessus, are responsible for deadly infectious diseases that kill over 1.5 million people each year across the world. A better understanding of the coding capacity of mycobacterial genomes is therefore necessary to shed increasing light on putative mechanisms of virulence, pathogenesis, and functional adaptations. DESCRIPTION: Here we describe the improved functional annotation coverage of 11 important mycobacterial genomes, many involved in human diseases including tuberculosis, leprosy, and nontuberculous mycobacterial (NTM) infections. Of the 11 mycobacterial genomes, we provide 9899 new functional annotations, compared to NCBI and TBDB annotations, for genes previously characterized as genes of unknown function, hypothetical, and hypothetical conserved proteins. Functional annotations are available at our newly developed web resource MycoBASE (Mycobacterial Annotation Server) at strong.ucdenver.edu/mycobase. CONCLUSION: Improved annotations allow for better understanding and interpretation of genomic and transcriptomic experiments, including analyzing the functional implications of insertions, deletions, and mutations, inferring the function of understudied genes, and determining functional changes resulting from differential expression studies. MycoBASE provides a valuable resource for mycobacterial researchers, through improved and searchable functional annotations and functional enrichment strategies. MycoBASE will be continually supported and updated to include new genomes, enabling a powerful resource to aid the quest to better understand these important pathogenic and environmental species.
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spelling pubmed-46902292015-12-25 MycoBASE: expanding the functional annotation coverage of mycobacterial genomes Garcia, Benjamin J. Datta, Gargi Davidson, Rebecca M. Strong, Michael BMC Genomics Database BACKGROUND: Central to most omic scale experiments is the interpretation and examination of resulting gene lists corresponding to differentially expressed, regulated, or observed gene or protein sets. Complicating interpretation is a lack of functional annotation assigned to a large percentage of many microbial genomes. This is particularly noticeable in mycobacterial genomes, which are significantly divergent from many of the microbial model species used for gene and protein functional characterization, but which are extremely important clinically. Mycobacterial species, ranging from M. tuberculosis to M. abscessus, are responsible for deadly infectious diseases that kill over 1.5 million people each year across the world. A better understanding of the coding capacity of mycobacterial genomes is therefore necessary to shed increasing light on putative mechanisms of virulence, pathogenesis, and functional adaptations. DESCRIPTION: Here we describe the improved functional annotation coverage of 11 important mycobacterial genomes, many involved in human diseases including tuberculosis, leprosy, and nontuberculous mycobacterial (NTM) infections. Of the 11 mycobacterial genomes, we provide 9899 new functional annotations, compared to NCBI and TBDB annotations, for genes previously characterized as genes of unknown function, hypothetical, and hypothetical conserved proteins. Functional annotations are available at our newly developed web resource MycoBASE (Mycobacterial Annotation Server) at strong.ucdenver.edu/mycobase. CONCLUSION: Improved annotations allow for better understanding and interpretation of genomic and transcriptomic experiments, including analyzing the functional implications of insertions, deletions, and mutations, inferring the function of understudied genes, and determining functional changes resulting from differential expression studies. MycoBASE provides a valuable resource for mycobacterial researchers, through improved and searchable functional annotations and functional enrichment strategies. MycoBASE will be continually supported and updated to include new genomes, enabling a powerful resource to aid the quest to better understand these important pathogenic and environmental species. BioMed Central 2015-12-24 /pmc/articles/PMC4690229/ /pubmed/26704706 http://dx.doi.org/10.1186/s12864-015-2311-9 Text en © Garcia et al. 2015 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 Database
Garcia, Benjamin J.
Datta, Gargi
Davidson, Rebecca M.
Strong, Michael
MycoBASE: expanding the functional annotation coverage of mycobacterial genomes
title MycoBASE: expanding the functional annotation coverage of mycobacterial genomes
title_full MycoBASE: expanding the functional annotation coverage of mycobacterial genomes
title_fullStr MycoBASE: expanding the functional annotation coverage of mycobacterial genomes
title_full_unstemmed MycoBASE: expanding the functional annotation coverage of mycobacterial genomes
title_short MycoBASE: expanding the functional annotation coverage of mycobacterial genomes
title_sort mycobase: expanding the functional annotation coverage of mycobacterial genomes
topic Database
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690229/
https://www.ncbi.nlm.nih.gov/pubmed/26704706
http://dx.doi.org/10.1186/s12864-015-2311-9
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