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Nucleic Acids Res. 2016 Jan 4;44(D1):D646-53. doi: 10.1093/nar/gkv1227. Epub 2015 Nov 17.

Enhanced annotations and features for comparing thousands of Pseudomonas genomes in the Pseudomonas genome database.

Author information

1
Department of Molecular Biology and Biochemistry, Simon Fraser University, Greater Vancouver, BC V5A 1S6, Canada gwinsor@sfu.ca.
2
Department of Molecular Biology and Biochemistry, Simon Fraser University, Greater Vancouver, BC V5A 1S6, Canada.
3
Department of Molecular Biology and Biochemistry, Simon Fraser University, Greater Vancouver, BC V5A 1S6, Canada brinkman@sfu.ca.

Abstract

The Pseudomonas Genome Database (http://www.pseudomonas.com) is well known for the application of community-based annotation approaches for producing a high-quality Pseudomonas aeruginosa PAO1 genome annotation, and facilitating whole-genome comparative analyses with other Pseudomonas strains. To aid analysis of potentially thousands of complete and draft genome assemblies, this database and analysis platform was upgraded to integrate curated genome annotations and isolate metadata with enhanced tools for larger scale comparative analysis and visualization. Manually curated gene annotations are supplemented with improved computational analyses that help identify putative drug targets and vaccine candidates or assist with evolutionary studies by identifying orthologs, pathogen-associated genes and genomic islands. The database schema has been updated to integrate isolate metadata that will facilitate more powerful analysis of genomes across datasets in the future. We continue to place an emphasis on providing high-quality updates to gene annotations through regular review of the scientific literature and using community-based approaches including a major new Pseudomonas community initiative for the assignment of high-quality gene ontology terms to genes. As we further expand from thousands of genomes, we plan to provide enhancements that will aid data visualization and analysis arising from whole-genome comparative studies including more pan-genome and population-based approaches.

PMID:
26578582
PMCID:
PMC4702867
DOI:
10.1093/nar/gkv1227
[Indexed for MEDLINE]
Free PMC Article

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