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CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing
The CRISPR–Cas system is a powerful genome editing tool that functions in a diverse array of organisms and cell types. The technology was initially developed to induce targeted mutations in DNA, but CRISPR–Cas has now been adapted to target nucleic acids for a range of purposes. CHOPCHOP is a web to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602426/ https://www.ncbi.nlm.nih.gov/pubmed/31106371 http://dx.doi.org/10.1093/nar/gkz365 |
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author | Labun, Kornel Montague, Tessa G Krause, Maximilian Torres Cleuren, Yamila N Tjeldnes, Håkon Valen, Eivind |
author_facet | Labun, Kornel Montague, Tessa G Krause, Maximilian Torres Cleuren, Yamila N Tjeldnes, Håkon Valen, Eivind |
author_sort | Labun, Kornel |
collection | PubMed |
description | The CRISPR–Cas system is a powerful genome editing tool that functions in a diverse array of organisms and cell types. The technology was initially developed to induce targeted mutations in DNA, but CRISPR–Cas has now been adapted to target nucleic acids for a range of purposes. CHOPCHOP is a web tool for identifying CRISPR–Cas single guide RNA (sgRNA) targets. In this major update of CHOPCHOP, we expand our toolbox beyond knockouts. We introduce functionality for targeting RNA with Cas13, which includes support for alternative transcript isoforms and RNA accessibility predictions. We incorporate new DNA targeting modes, including CRISPR activation/repression, targeted enrichment of loci for long-read sequencing, and prediction of Cas9 repair outcomes. Finally, we expand our results page visualization to reveal alternative isoforms and downstream ATG sites, which will aid users in avoiding the expression of truncated proteins. The CHOPCHOP web tool now supports over 200 genomes and we have released a command-line script for running larger jobs and handling unsupported genomes. CHOPCHOP v3 can be found at https://chopchop.cbu.uib.no |
format | Online Article Text |
id | pubmed-6602426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66024262019-07-05 CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing Labun, Kornel Montague, Tessa G Krause, Maximilian Torres Cleuren, Yamila N Tjeldnes, Håkon Valen, Eivind Nucleic Acids Res Web Server Issue The CRISPR–Cas system is a powerful genome editing tool that functions in a diverse array of organisms and cell types. The technology was initially developed to induce targeted mutations in DNA, but CRISPR–Cas has now been adapted to target nucleic acids for a range of purposes. CHOPCHOP is a web tool for identifying CRISPR–Cas single guide RNA (sgRNA) targets. In this major update of CHOPCHOP, we expand our toolbox beyond knockouts. We introduce functionality for targeting RNA with Cas13, which includes support for alternative transcript isoforms and RNA accessibility predictions. We incorporate new DNA targeting modes, including CRISPR activation/repression, targeted enrichment of loci for long-read sequencing, and prediction of Cas9 repair outcomes. Finally, we expand our results page visualization to reveal alternative isoforms and downstream ATG sites, which will aid users in avoiding the expression of truncated proteins. The CHOPCHOP web tool now supports over 200 genomes and we have released a command-line script for running larger jobs and handling unsupported genomes. CHOPCHOP v3 can be found at https://chopchop.cbu.uib.no Oxford University Press 2019-07-02 2019-05-20 /pmc/articles/PMC6602426/ /pubmed/31106371 http://dx.doi.org/10.1093/nar/gkz365 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Web Server Issue Labun, Kornel Montague, Tessa G Krause, Maximilian Torres Cleuren, Yamila N Tjeldnes, Håkon Valen, Eivind CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing |
title | CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing |
title_full | CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing |
title_fullStr | CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing |
title_full_unstemmed | CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing |
title_short | CHOPCHOP v3: expanding the CRISPR web toolbox beyond genome editing |
title_sort | chopchop v3: expanding the crispr web toolbox beyond genome editing |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602426/ https://www.ncbi.nlm.nih.gov/pubmed/31106371 http://dx.doi.org/10.1093/nar/gkz365 |
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