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dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells
With the technology's accessibility and ease of use, CRISPR has been employed widely in many different organisms and experimental settings. As a result, thousands of publications have used CRISPR to make specific genetic perturbations, establishing in itself a resource of validated guide RNA se...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779039/ https://www.ncbi.nlm.nih.gov/pubmed/33051688 http://dx.doi.org/10.1093/nar/gkaa848 |
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author | Gooden, Alexander A Evans, Christine N Sheets, Timothy P Clapp, Michelle E Chari, Raj |
author_facet | Gooden, Alexander A Evans, Christine N Sheets, Timothy P Clapp, Michelle E Chari, Raj |
author_sort | Gooden, Alexander A |
collection | PubMed |
description | With the technology's accessibility and ease of use, CRISPR has been employed widely in many different organisms and experimental settings. As a result, thousands of publications have used CRISPR to make specific genetic perturbations, establishing in itself a resource of validated guide RNA sequences. While numerous computational tools to assist in the design and identification of candidate guide RNAs exist, these are still just at best predictions and generally, researchers inevitably will test multiple sequences for functional activity. Here, we present dbGuide (https://sgrnascorer.cancer.gov/dbguide), a database of functionally validated guide RNA sequences for CRISPR/Cas9-based knockout in human and mouse. Our database not only contains computationally determined candidate guide RNA sequences, but of even greater value, over 4000 sequences which have been functionally validated either through direct amplicon sequencing or manual curation of literature from over 1000 publications. Finally, our established framework will allow for continual addition of newly published and experimentally validated guide RNA sequences for CRISPR/Cas9-based knockout as well as incorporation of sequences from different gene editing systems, additional species and other types of site-specific functionalities such as base editing, gene activation, repression and epigenetic modification. |
format | Online Article Text |
id | pubmed-7779039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77790392021-01-07 dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells Gooden, Alexander A Evans, Christine N Sheets, Timothy P Clapp, Michelle E Chari, Raj Nucleic Acids Res Database Issue With the technology's accessibility and ease of use, CRISPR has been employed widely in many different organisms and experimental settings. As a result, thousands of publications have used CRISPR to make specific genetic perturbations, establishing in itself a resource of validated guide RNA sequences. While numerous computational tools to assist in the design and identification of candidate guide RNAs exist, these are still just at best predictions and generally, researchers inevitably will test multiple sequences for functional activity. Here, we present dbGuide (https://sgrnascorer.cancer.gov/dbguide), a database of functionally validated guide RNA sequences for CRISPR/Cas9-based knockout in human and mouse. Our database not only contains computationally determined candidate guide RNA sequences, but of even greater value, over 4000 sequences which have been functionally validated either through direct amplicon sequencing or manual curation of literature from over 1000 publications. Finally, our established framework will allow for continual addition of newly published and experimentally validated guide RNA sequences for CRISPR/Cas9-based knockout as well as incorporation of sequences from different gene editing systems, additional species and other types of site-specific functionalities such as base editing, gene activation, repression and epigenetic modification. Oxford University Press 2020-10-13 /pmc/articles/PMC7779039/ /pubmed/33051688 http://dx.doi.org/10.1093/nar/gkaa848 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), 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 | Database Issue Gooden, Alexander A Evans, Christine N Sheets, Timothy P Clapp, Michelle E Chari, Raj dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells |
title | dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells |
title_full | dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells |
title_fullStr | dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells |
title_full_unstemmed | dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells |
title_short | dbGuide: a database of functionally validated guide RNAs for genome editing in human and mouse cells |
title_sort | dbguide: a database of functionally validated guide rnas for genome editing in human and mouse cells |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779039/ https://www.ncbi.nlm.nih.gov/pubmed/33051688 http://dx.doi.org/10.1093/nar/gkaa848 |
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