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Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches
We present a novel genome-wide off-target prediction method named Extru-seq and compare it with cell-based (GUIDE-seq), in vitro (Digenome-seq), and in silico methods using promiscuous guide RNAs with large numbers of valid off-target sites. Extru-seq demonstrates a high validation rate and retentio...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832775/ https://www.ncbi.nlm.nih.gov/pubmed/36627653 http://dx.doi.org/10.1186/s13059-022-02842-4 |
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author | Kwon, Jeonghun Kim, Minyoung Hwang, Woochang Jo, Anna Hwang, Gue-Ho Jung, Minhee Kim, Un Gi Cui, Gang Kim, Heonseok Eom, Joon-Ho Hur, Junho K. Lee, Junwon Kim, Youngho Kim, Jin-soo Bae, Sangsu Lee, Jungjoon K. |
author_facet | Kwon, Jeonghun Kim, Minyoung Hwang, Woochang Jo, Anna Hwang, Gue-Ho Jung, Minhee Kim, Un Gi Cui, Gang Kim, Heonseok Eom, Joon-Ho Hur, Junho K. Lee, Junwon Kim, Youngho Kim, Jin-soo Bae, Sangsu Lee, Jungjoon K. |
author_sort | Kwon, Jeonghun |
collection | PubMed |
description | We present a novel genome-wide off-target prediction method named Extru-seq and compare it with cell-based (GUIDE-seq), in vitro (Digenome-seq), and in silico methods using promiscuous guide RNAs with large numbers of valid off-target sites. Extru-seq demonstrates a high validation rate and retention of information about the intracellular environment, both beneficial characteristics of cell-based methods. Extru-seq also shows a low miss rate and could easily be performed in clinically relevant cell types with little optimization, which are major positive features of the in vitro methods. In summary, Extru-seq shows beneficial features of cell-based and in vitro methods. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-022-02842-4. |
format | Online Article Text |
id | pubmed-9832775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98327752023-01-12 Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches Kwon, Jeonghun Kim, Minyoung Hwang, Woochang Jo, Anna Hwang, Gue-Ho Jung, Minhee Kim, Un Gi Cui, Gang Kim, Heonseok Eom, Joon-Ho Hur, Junho K. Lee, Junwon Kim, Youngho Kim, Jin-soo Bae, Sangsu Lee, Jungjoon K. Genome Biol Method We present a novel genome-wide off-target prediction method named Extru-seq and compare it with cell-based (GUIDE-seq), in vitro (Digenome-seq), and in silico methods using promiscuous guide RNAs with large numbers of valid off-target sites. Extru-seq demonstrates a high validation rate and retention of information about the intracellular environment, both beneficial characteristics of cell-based methods. Extru-seq also shows a low miss rate and could easily be performed in clinically relevant cell types with little optimization, which are major positive features of the in vitro methods. In summary, Extru-seq shows beneficial features of cell-based and in vitro methods. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-022-02842-4. BioMed Central 2023-01-10 /pmc/articles/PMC9832775/ /pubmed/36627653 http://dx.doi.org/10.1186/s13059-022-02842-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 | Method Kwon, Jeonghun Kim, Minyoung Hwang, Woochang Jo, Anna Hwang, Gue-Ho Jung, Minhee Kim, Un Gi Cui, Gang Kim, Heonseok Eom, Joon-Ho Hur, Junho K. Lee, Junwon Kim, Youngho Kim, Jin-soo Bae, Sangsu Lee, Jungjoon K. Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches |
title | Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches |
title_full | Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches |
title_fullStr | Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches |
title_full_unstemmed | Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches |
title_short | Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches |
title_sort | extru-seq: a method for predicting genome-wide cas9 off-target sites with advantages of both cell-based and in vitro approaches |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832775/ https://www.ncbi.nlm.nih.gov/pubmed/36627653 http://dx.doi.org/10.1186/s13059-022-02842-4 |
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