2013
DOI: 10.4238/2013.august.16.2
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PANNOTATOR: an automated tool for annotation of pan-genomes

Abstract: ABSTRACT. Due to next-generation sequence technologies, sequencing of bacterial genomes is no longer one of the main bottlenecks in bacterial research and the number of new genomes deposited in public databases continues to increase at an accelerating rate. Among these new genomes, several belong to the same species and were generated for pan-genomic studies. A pan-genomic study allows investigation of strain phenotypic differences based on genotypic differences. Along with a need for good assembly quality, it… Show more

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Cited by 24 publications
(13 citation statements)
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“…pseudotuberculosis MB11 as the reference genome because its assembly was confirmed by the in vitro optical map. The high-quality scaffolds were submitted to the web software Pannotator [ 53 ] for automatic annotation using the C . pseudotuberculosis 316 as the reference genome.…”
Section: Methodsmentioning
confidence: 99%
“…pseudotuberculosis MB11 as the reference genome because its assembly was confirmed by the in vitro optical map. The high-quality scaffolds were submitted to the web software Pannotator [ 53 ] for automatic annotation using the C . pseudotuberculosis 316 as the reference genome.…”
Section: Methodsmentioning
confidence: 99%
“…When specified, an attempt will be made to inherit all annotations from the reference genome and also propagate gene names. Because gene names are used inconsistently across species, neither the SEED nor RAST has ever attempted to propagate them (32). For example, the gene sir A of Salmonella is also known as uvr Y in E. coli or gac A in Pseudomonas .…”
Section: Future Developmentsmentioning
confidence: 99%
“…An automatic annotation was first conducted using the online software Pannotator [ 13 ], which provided the .fasta files for the assembled genomes and a reference .embl file for C. pseudotuberculosis 316. The results were then manually curated to meet the gene annotation standards set by UniProt [ 14 ] using Artemis software [ 15 ] to visualize the coding sequences.…”
Section: Genome Sequencing Informationmentioning
confidence: 99%