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E-TALEN: a web tool to design TALENs for genome engineering

Use of transcription activator-like effector nucleases (TALENs) is a promising new technique in the field of targeted genome engineering, editing and reverse genetics. Its applications span from introducing knockout mutations to endogenous tagging of proteins and targeted excision repair. Owing to t...

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Autores principales: Heigwer, Florian, Kerr, Grainne, Walther, Nike, Glaeser, Kathrin, Pelz, Oliver, Breinig, Marco, Boutros, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814377/
https://www.ncbi.nlm.nih.gov/pubmed/24003033
http://dx.doi.org/10.1093/nar/gkt789
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author Heigwer, Florian
Kerr, Grainne
Walther, Nike
Glaeser, Kathrin
Pelz, Oliver
Breinig, Marco
Boutros, Michael
author_facet Heigwer, Florian
Kerr, Grainne
Walther, Nike
Glaeser, Kathrin
Pelz, Oliver
Breinig, Marco
Boutros, Michael
author_sort Heigwer, Florian
collection PubMed
description Use of transcription activator-like effector nucleases (TALENs) is a promising new technique in the field of targeted genome engineering, editing and reverse genetics. Its applications span from introducing knockout mutations to endogenous tagging of proteins and targeted excision repair. Owing to this wide range of possible applications, there is a need for fast and user-friendly TALEN design tools. We developed E-TALEN (http://www.e-talen.org), a web-based tool to design TALENs for experiments of varying scale. E-TALEN enables the design of TALENs against a single target or a large number of target genes. We significantly extended previously published design concepts to consider genomic context and different applications. E-TALEN guides the user through an end-to-end design process of de novo TALEN pairs, which are specific to a certain sequence or genomic locus. Furthermore, E-TALEN offers a functionality to predict targeting and specificity for existing TALENs. Owing to the computational complexity of many of the steps in the design of TALENs, particular emphasis has been put on the implementation of fast yet accurate algorithms. We implemented a user-friendly interface, from the input parameters to the presentation of results. An additional feature of E-TALEN is the in-built sequence and annotation database available for many organisms, including human, mouse, zebrafish, Drosophila and Arabidopsis, which can be extended in the future.
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spelling pubmed-38143772013-12-27 E-TALEN: a web tool to design TALENs for genome engineering Heigwer, Florian Kerr, Grainne Walther, Nike Glaeser, Kathrin Pelz, Oliver Breinig, Marco Boutros, Michael Nucleic Acids Res Methods Online Use of transcription activator-like effector nucleases (TALENs) is a promising new technique in the field of targeted genome engineering, editing and reverse genetics. Its applications span from introducing knockout mutations to endogenous tagging of proteins and targeted excision repair. Owing to this wide range of possible applications, there is a need for fast and user-friendly TALEN design tools. We developed E-TALEN (http://www.e-talen.org), a web-based tool to design TALENs for experiments of varying scale. E-TALEN enables the design of TALENs against a single target or a large number of target genes. We significantly extended previously published design concepts to consider genomic context and different applications. E-TALEN guides the user through an end-to-end design process of de novo TALEN pairs, which are specific to a certain sequence or genomic locus. Furthermore, E-TALEN offers a functionality to predict targeting and specificity for existing TALENs. Owing to the computational complexity of many of the steps in the design of TALENs, particular emphasis has been put on the implementation of fast yet accurate algorithms. We implemented a user-friendly interface, from the input parameters to the presentation of results. An additional feature of E-TALEN is the in-built sequence and annotation database available for many organisms, including human, mouse, zebrafish, Drosophila and Arabidopsis, which can be extended in the future. Oxford University Press 2013-11 2013-09-03 /pmc/articles/PMC3814377/ /pubmed/24003033 http://dx.doi.org/10.1093/nar/gkt789 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Online
Heigwer, Florian
Kerr, Grainne
Walther, Nike
Glaeser, Kathrin
Pelz, Oliver
Breinig, Marco
Boutros, Michael
E-TALEN: a web tool to design TALENs for genome engineering
title E-TALEN: a web tool to design TALENs for genome engineering
title_full E-TALEN: a web tool to design TALENs for genome engineering
title_fullStr E-TALEN: a web tool to design TALENs for genome engineering
title_full_unstemmed E-TALEN: a web tool to design TALENs for genome engineering
title_short E-TALEN: a web tool to design TALENs for genome engineering
title_sort e-talen: a web tool to design talens for genome engineering
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814377/
https://www.ncbi.nlm.nih.gov/pubmed/24003033
http://dx.doi.org/10.1093/nar/gkt789
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