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RATT: Rapid Annotation Transfer Tool

Second-generation sequencing technologies have made large-scale sequencing projects commonplace. However, making use of these datasets often requires gene function to be ascribed genome wide. Although tool development has kept pace with the changes in sequence production, for tasks such as mapping,...

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Detalles Bibliográficos
Autores principales: Otto, Thomas D., Dillon, Gary P., Degrave, Wim S., Berriman, Matthew
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089447/
https://www.ncbi.nlm.nih.gov/pubmed/21306991
http://dx.doi.org/10.1093/nar/gkq1268
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author Otto, Thomas D.
Dillon, Gary P.
Degrave, Wim S.
Berriman, Matthew
author_facet Otto, Thomas D.
Dillon, Gary P.
Degrave, Wim S.
Berriman, Matthew
author_sort Otto, Thomas D.
collection PubMed
description Second-generation sequencing technologies have made large-scale sequencing projects commonplace. However, making use of these datasets often requires gene function to be ascribed genome wide. Although tool development has kept pace with the changes in sequence production, for tasks such as mapping, de novo assembly or visualization, genome annotation remains a challenge. We have developed a method to rapidly provide accurate annotation for new genomes using previously annotated genomes as a reference. The method, implemented in a tool called RATT (Rapid Annotation Transfer Tool), transfers annotations from a high-quality reference to a new genome on the basis of conserved synteny. We demonstrate that a Mycobacterium tuberculosis genome or a single 2.5 Mb chromosome from a malaria parasite can be annotated in less than five minutes with only modest computational resources. RATT is available at http://ratt.sourceforge.net.
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spelling pubmed-30894472011-05-09 RATT: Rapid Annotation Transfer Tool Otto, Thomas D. Dillon, Gary P. Degrave, Wim S. Berriman, Matthew Nucleic Acids Res Methods Online Second-generation sequencing technologies have made large-scale sequencing projects commonplace. However, making use of these datasets often requires gene function to be ascribed genome wide. Although tool development has kept pace with the changes in sequence production, for tasks such as mapping, de novo assembly or visualization, genome annotation remains a challenge. We have developed a method to rapidly provide accurate annotation for new genomes using previously annotated genomes as a reference. The method, implemented in a tool called RATT (Rapid Annotation Transfer Tool), transfers annotations from a high-quality reference to a new genome on the basis of conserved synteny. We demonstrate that a Mycobacterium tuberculosis genome or a single 2.5 Mb chromosome from a malaria parasite can be annotated in less than five minutes with only modest computational resources. RATT is available at http://ratt.sourceforge.net. Oxford University Press 2011-05 2011-02-08 /pmc/articles/PMC3089447/ /pubmed/21306991 http://dx.doi.org/10.1093/nar/gkq1268 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Otto, Thomas D.
Dillon, Gary P.
Degrave, Wim S.
Berriman, Matthew
RATT: Rapid Annotation Transfer Tool
title RATT: Rapid Annotation Transfer Tool
title_full RATT: Rapid Annotation Transfer Tool
title_fullStr RATT: Rapid Annotation Transfer Tool
title_full_unstemmed RATT: Rapid Annotation Transfer Tool
title_short RATT: Rapid Annotation Transfer Tool
title_sort ratt: rapid annotation transfer tool
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089447/
https://www.ncbi.nlm.nih.gov/pubmed/21306991
http://dx.doi.org/10.1093/nar/gkq1268
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