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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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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. |
format | Online Article Text |
id | pubmed-5658704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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