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ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens

High-throughput CRISPR-Cas9 knockout screens are widely used to evaluate gene essentiality in cancer research. Here we introduce a probabilistic modeling framework, Analysis of CRISPR-based Essentiality (ACE), that accounts for multiple sources of variation in CRISPR-Cas9 screens and enables new sta...

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Autores principales: Hutton, Elizabeth R., Vakoc, Christopher R., Siepel, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459512/
https://www.ncbi.nlm.nih.gov/pubmed/34556174
http://dx.doi.org/10.1186/s13059-021-02491-z
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author Hutton, Elizabeth R.
Vakoc, Christopher R.
Siepel, Adam
author_facet Hutton, Elizabeth R.
Vakoc, Christopher R.
Siepel, Adam
author_sort Hutton, Elizabeth R.
collection PubMed
description High-throughput CRISPR-Cas9 knockout screens are widely used to evaluate gene essentiality in cancer research. Here we introduce a probabilistic modeling framework, Analysis of CRISPR-based Essentiality (ACE), that accounts for multiple sources of variation in CRISPR-Cas9 screens and enables new statistical tests for essentiality. We show using simulations that ACE is effective at predicting both absolute and differential essentiality. When applied to publicly available data, ACE identifies known and novel candidates for genotype-specific essentiality, including RNA m(6)-A methyltransferases that exhibit enhanced essentiality in the presence of inactivating TP53 mutations. ACE provides a robust framework for identifying genes responsive to subtype-specific therapeutic targeting. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13059-021-02491-z).
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spelling pubmed-84595122021-09-23 ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens Hutton, Elizabeth R. Vakoc, Christopher R. Siepel, Adam Genome Biol Software High-throughput CRISPR-Cas9 knockout screens are widely used to evaluate gene essentiality in cancer research. Here we introduce a probabilistic modeling framework, Analysis of CRISPR-based Essentiality (ACE), that accounts for multiple sources of variation in CRISPR-Cas9 screens and enables new statistical tests for essentiality. We show using simulations that ACE is effective at predicting both absolute and differential essentiality. When applied to publicly available data, ACE identifies known and novel candidates for genotype-specific essentiality, including RNA m(6)-A methyltransferases that exhibit enhanced essentiality in the presence of inactivating TP53 mutations. ACE provides a robust framework for identifying genes responsive to subtype-specific therapeutic targeting. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13059-021-02491-z). BioMed Central 2021-09-23 /pmc/articles/PMC8459512/ /pubmed/34556174 http://dx.doi.org/10.1186/s13059-021-02491-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Software
Hutton, Elizabeth R.
Vakoc, Christopher R.
Siepel, Adam
ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens
title ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens
title_full ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens
title_fullStr ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens
title_full_unstemmed ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens
title_short ACE: a probabilistic model for characterizing gene-level essentiality in CRISPR screens
title_sort ace: a probabilistic model for characterizing gene-level essentiality in crispr screens
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459512/
https://www.ncbi.nlm.nih.gov/pubmed/34556174
http://dx.doi.org/10.1186/s13059-021-02491-z
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