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Minimal genome-wide human CRISPR-Cas9 library
CRISPR guide RNA libraries have been iteratively improved to provide increasingly efficient reagents, although their large size is a barrier for many applications. We design an optimised minimal genome-wide human CRISPR-Cas9 library (MinLibCas9) by mining existing large-scale gene loss-of-function d...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818936/ https://www.ncbi.nlm.nih.gov/pubmed/33478580 http://dx.doi.org/10.1186/s13059-021-02268-4 |
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author | Gonçalves, Emanuel Thomas, Mark Behan, Fiona M. Picco, Gabriele Pacini, Clare Allen, Felicity Vinceti, Alessandro Sharma, Mamta Jackson, David A. Price, Stacey Beaver, Charlotte M. Dovey, Oliver Parry-Smith, David Iorio, Francesco Parts, Leopold Yusa, Kosuke Garnett, Mathew J. |
author_facet | Gonçalves, Emanuel Thomas, Mark Behan, Fiona M. Picco, Gabriele Pacini, Clare Allen, Felicity Vinceti, Alessandro Sharma, Mamta Jackson, David A. Price, Stacey Beaver, Charlotte M. Dovey, Oliver Parry-Smith, David Iorio, Francesco Parts, Leopold Yusa, Kosuke Garnett, Mathew J. |
author_sort | Gonçalves, Emanuel |
collection | PubMed |
description | CRISPR guide RNA libraries have been iteratively improved to provide increasingly efficient reagents, although their large size is a barrier for many applications. We design an optimised minimal genome-wide human CRISPR-Cas9 library (MinLibCas9) by mining existing large-scale gene loss-of-function datasets, resulting in a greater than 42% reduction in size compared to other CRISPR-Cas9 libraries while preserving assay sensitivity and specificity. MinLibCas9 provides backward compatibility with existing datasets, increases the dynamic range of CRISPR-Cas9 screens and extends their application to complex models and assays. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02268-4. |
format | Online Article Text |
id | pubmed-7818936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78189362021-01-22 Minimal genome-wide human CRISPR-Cas9 library Gonçalves, Emanuel Thomas, Mark Behan, Fiona M. Picco, Gabriele Pacini, Clare Allen, Felicity Vinceti, Alessandro Sharma, Mamta Jackson, David A. Price, Stacey Beaver, Charlotte M. Dovey, Oliver Parry-Smith, David Iorio, Francesco Parts, Leopold Yusa, Kosuke Garnett, Mathew J. Genome Biol Short Report CRISPR guide RNA libraries have been iteratively improved to provide increasingly efficient reagents, although their large size is a barrier for many applications. We design an optimised minimal genome-wide human CRISPR-Cas9 library (MinLibCas9) by mining existing large-scale gene loss-of-function datasets, resulting in a greater than 42% reduction in size compared to other CRISPR-Cas9 libraries while preserving assay sensitivity and specificity. MinLibCas9 provides backward compatibility with existing datasets, increases the dynamic range of CRISPR-Cas9 screens and extends their application to complex models and assays. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02268-4. BioMed Central 2021-01-21 /pmc/articles/PMC7818936/ /pubmed/33478580 http://dx.doi.org/10.1186/s13059-021-02268-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Short Report Gonçalves, Emanuel Thomas, Mark Behan, Fiona M. Picco, Gabriele Pacini, Clare Allen, Felicity Vinceti, Alessandro Sharma, Mamta Jackson, David A. Price, Stacey Beaver, Charlotte M. Dovey, Oliver Parry-Smith, David Iorio, Francesco Parts, Leopold Yusa, Kosuke Garnett, Mathew J. Minimal genome-wide human CRISPR-Cas9 library |
title | Minimal genome-wide human CRISPR-Cas9 library |
title_full | Minimal genome-wide human CRISPR-Cas9 library |
title_fullStr | Minimal genome-wide human CRISPR-Cas9 library |
title_full_unstemmed | Minimal genome-wide human CRISPR-Cas9 library |
title_short | Minimal genome-wide human CRISPR-Cas9 library |
title_sort | minimal genome-wide human crispr-cas9 library |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818936/ https://www.ncbi.nlm.nih.gov/pubmed/33478580 http://dx.doi.org/10.1186/s13059-021-02268-4 |
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