Cargando…

Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library

CRISPR-based genetic screens revolutionized our ability to genetically probe cell biology. We present a protocol to conduct genome-scale chemogenomic dropout CRISPR screens in the human RPE1-hTERT p53(−/−) cell line. We use the TKOv3 library, which contains 70,948 sgRNAs targeting 18,053 genes. Here...

Descripción completa

Detalles Bibliográficos
Autores principales: Olivieri, Michele, Durocher, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868615/
https://www.ncbi.nlm.nih.gov/pubmed/33598657
http://dx.doi.org/10.1016/j.xpro.2021.100321
_version_ 1783648485864636416
author Olivieri, Michele
Durocher, Daniel
author_facet Olivieri, Michele
Durocher, Daniel
author_sort Olivieri, Michele
collection PubMed
description CRISPR-based genetic screens revolutionized our ability to genetically probe cell biology. We present a protocol to conduct genome-scale chemogenomic dropout CRISPR screens in the human RPE1-hTERT p53(−/−) cell line. We use the TKOv3 library, which contains 70,948 sgRNAs targeting 18,053 genes. Here, we describe how to set up the screen, the reagents required, and how to sequence and analyze the results. This protocol can be customized for other libraries, cell lines, and sequencing instruments. For complete details on the use and execution of this protocol, please refer to Olivieri et al. (2020).
format Online
Article
Text
id pubmed-7868615
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-78686152021-02-16 Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library Olivieri, Michele Durocher, Daniel STAR Protoc Protocol CRISPR-based genetic screens revolutionized our ability to genetically probe cell biology. We present a protocol to conduct genome-scale chemogenomic dropout CRISPR screens in the human RPE1-hTERT p53(−/−) cell line. We use the TKOv3 library, which contains 70,948 sgRNAs targeting 18,053 genes. Here, we describe how to set up the screen, the reagents required, and how to sequence and analyze the results. This protocol can be customized for other libraries, cell lines, and sequencing instruments. For complete details on the use and execution of this protocol, please refer to Olivieri et al. (2020). Elsevier 2021-02-05 /pmc/articles/PMC7868615/ /pubmed/33598657 http://dx.doi.org/10.1016/j.xpro.2021.100321 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Olivieri, Michele
Durocher, Daniel
Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library
title Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library
title_full Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library
title_fullStr Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library
title_full_unstemmed Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library
title_short Genome-scale chemogenomic CRISPR screens in human cells using the TKOv3 library
title_sort genome-scale chemogenomic crispr screens in human cells using the tkov3 library
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868615/
https://www.ncbi.nlm.nih.gov/pubmed/33598657
http://dx.doi.org/10.1016/j.xpro.2021.100321
work_keys_str_mv AT olivierimichele genomescalechemogenomiccrisprscreensinhumancellsusingthetkov3library
AT durocherdaniel genomescalechemogenomiccrisprscreensinhumancellsusingthetkov3library