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CRISPR/Cas9 screening using unique molecular identifiers

Loss‐of‐function screening by CRISPR/Cas9 gene knockout with pooled, lentiviral guide libraries is a widely applicable method for systematic identification of genes contributing to diverse cellular phenotypes. Here, Random Sequence Labels (RSLs) are incorporated into the guide library, which act as...

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Detalles Bibliográficos
Autores principales: Schmierer, Bernhard, Botla, Sandeep K, Zhang, Jilin, Turunen, Mikko, Kivioja, Teemu, Taipale, Jussi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658704/
https://www.ncbi.nlm.nih.gov/pubmed/28993443
http://dx.doi.org/10.15252/msb.20177834
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author Schmierer, Bernhard
Botla, Sandeep K
Zhang, Jilin
Turunen, Mikko
Kivioja, Teemu
Taipale, Jussi
author_facet Schmierer, Bernhard
Botla, Sandeep K
Zhang, Jilin
Turunen, Mikko
Kivioja, Teemu
Taipale, Jussi
author_sort Schmierer, Bernhard
collection PubMed
description Loss‐of‐function screening by CRISPR/Cas9 gene knockout with pooled, lentiviral guide libraries is a widely applicable method for systematic identification of genes contributing to diverse cellular phenotypes. Here, Random Sequence Labels (RSLs) are incorporated into the guide library, which act as unique molecular identifiers (UMIs) to allow massively parallel lineage tracing and lineage dropout screening. RSLs greatly improve the reproducibility of results by increasing both the precision and the accuracy of screens. They reduce the number of cells needed to reach a set statistical power, or allow a more robust screen using the same number of cells.
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spelling pubmed-56587042017-11-01 CRISPR/Cas9 screening using unique molecular identifiers Schmierer, Bernhard Botla, Sandeep K Zhang, Jilin Turunen, Mikko Kivioja, Teemu Taipale, Jussi Mol Syst Biol Method Loss‐of‐function screening by CRISPR/Cas9 gene knockout with pooled, lentiviral guide libraries is a widely applicable method for systematic identification of genes contributing to diverse cellular phenotypes. Here, Random Sequence Labels (RSLs) are incorporated into the guide library, which act as unique molecular identifiers (UMIs) to allow massively parallel lineage tracing and lineage dropout screening. RSLs greatly improve the reproducibility of results by increasing both the precision and the accuracy of screens. They reduce the number of cells needed to reach a set statistical power, or allow a more robust screen using the same number of cells. John Wiley and Sons Inc. 2017-10-09 /pmc/articles/PMC5658704/ /pubmed/28993443 http://dx.doi.org/10.15252/msb.20177834 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method
Schmierer, Bernhard
Botla, Sandeep K
Zhang, Jilin
Turunen, Mikko
Kivioja, Teemu
Taipale, Jussi
CRISPR/Cas9 screening using unique molecular identifiers
title CRISPR/Cas9 screening using unique molecular identifiers
title_full CRISPR/Cas9 screening using unique molecular identifiers
title_fullStr CRISPR/Cas9 screening using unique molecular identifiers
title_full_unstemmed CRISPR/Cas9 screening using unique molecular identifiers
title_short CRISPR/Cas9 screening using unique molecular identifiers
title_sort crispr/cas9 screening using unique molecular identifiers
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658704/
https://www.ncbi.nlm.nih.gov/pubmed/28993443
http://dx.doi.org/10.15252/msb.20177834
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