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A benchmark of computational CRISPR-Cas9 guide design methods
The popularity of CRISPR-based gene editing has resulted in an abundance of tools to design CRISPR-Cas9 guides. This is also driven by the fact that designing highly specific and efficient guides is a crucial, but not trivial, task in using CRISPR for gene editing. Here, we thoroughly analyse the pe...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6738662/ https://www.ncbi.nlm.nih.gov/pubmed/31465436 http://dx.doi.org/10.1371/journal.pcbi.1007274 |
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author | Bradford, Jacob Perrin, Dimitri |
author_facet | Bradford, Jacob Perrin, Dimitri |
author_sort | Bradford, Jacob |
collection | PubMed |
description | The popularity of CRISPR-based gene editing has resulted in an abundance of tools to design CRISPR-Cas9 guides. This is also driven by the fact that designing highly specific and efficient guides is a crucial, but not trivial, task in using CRISPR for gene editing. Here, we thoroughly analyse the performance of 18 design tools. They are evaluated based on runtime performance, compute requirements, and guides generated. To achieve this, we implemented a method for auditing system resources while a given tool executes, and tested each tool on datasets of increasing size, derived from the mouse genome. We found that only five tools had a computational performance that would allow them to analyse an entire genome in a reasonable time, and without exhausting computing resources. There was wide variation in the guides identified, with some tools reporting every possible guide while others filtered for predicted efficiency. Some tools also failed to exclude guides that would target multiple positions in the genome. We also considered two collections with over a thousand guides each, for which experimental data is available. There is a lot of variation in performance between the datasets, but the relative order of the tools is partially conserved. Importantly, the most striking result is a lack of consensus between the tools. Our results show that CRISPR-Cas9 guide design tools need further work in order to achieve rapid whole-genome analysis and that improvements in guide design will likely require combining multiple approaches. |
format | Online Article Text |
id | pubmed-6738662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67386622019-09-20 A benchmark of computational CRISPR-Cas9 guide design methods Bradford, Jacob Perrin, Dimitri PLoS Comput Biol Research Article The popularity of CRISPR-based gene editing has resulted in an abundance of tools to design CRISPR-Cas9 guides. This is also driven by the fact that designing highly specific and efficient guides is a crucial, but not trivial, task in using CRISPR for gene editing. Here, we thoroughly analyse the performance of 18 design tools. They are evaluated based on runtime performance, compute requirements, and guides generated. To achieve this, we implemented a method for auditing system resources while a given tool executes, and tested each tool on datasets of increasing size, derived from the mouse genome. We found that only five tools had a computational performance that would allow them to analyse an entire genome in a reasonable time, and without exhausting computing resources. There was wide variation in the guides identified, with some tools reporting every possible guide while others filtered for predicted efficiency. Some tools also failed to exclude guides that would target multiple positions in the genome. We also considered two collections with over a thousand guides each, for which experimental data is available. There is a lot of variation in performance between the datasets, but the relative order of the tools is partially conserved. Importantly, the most striking result is a lack of consensus between the tools. Our results show that CRISPR-Cas9 guide design tools need further work in order to achieve rapid whole-genome analysis and that improvements in guide design will likely require combining multiple approaches. Public Library of Science 2019-08-29 /pmc/articles/PMC6738662/ /pubmed/31465436 http://dx.doi.org/10.1371/journal.pcbi.1007274 Text en © 2019 Bradford, Perrin 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Bradford, Jacob Perrin, Dimitri A benchmark of computational CRISPR-Cas9 guide design methods |
title | A benchmark of computational CRISPR-Cas9 guide design methods |
title_full | A benchmark of computational CRISPR-Cas9 guide design methods |
title_fullStr | A benchmark of computational CRISPR-Cas9 guide design methods |
title_full_unstemmed | A benchmark of computational CRISPR-Cas9 guide design methods |
title_short | A benchmark of computational CRISPR-Cas9 guide design methods |
title_sort | benchmark of computational crispr-cas9 guide design methods |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6738662/ https://www.ncbi.nlm.nih.gov/pubmed/31465436 http://dx.doi.org/10.1371/journal.pcbi.1007274 |
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