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BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models

BACKGROUND: In the CRISPR-Cas9 system, the efficiency of genetic modifications has been found to vary depending on the single guide RNA (sgRNA) used. A variety of sgRNA properties have been found to be predictive of CRISPR cleavage efficiency, including the position-specific sequence composition of...

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Autores principales: Zarate, Oscar A., Yang, Yiben, Wang, Xiaozhong, Wang, Ji-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597963/
https://www.ncbi.nlm.nih.gov/pubmed/36289480
http://dx.doi.org/10.1186/s12859-022-04998-z
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author Zarate, Oscar A.
Yang, Yiben
Wang, Xiaozhong
Wang, Ji-Ping
author_facet Zarate, Oscar A.
Yang, Yiben
Wang, Xiaozhong
Wang, Ji-Ping
author_sort Zarate, Oscar A.
collection PubMed
description BACKGROUND: In the CRISPR-Cas9 system, the efficiency of genetic modifications has been found to vary depending on the single guide RNA (sgRNA) used. A variety of sgRNA properties have been found to be predictive of CRISPR cleavage efficiency, including the position-specific sequence composition of sgRNAs, global sgRNA sequence properties, and thermodynamic features. While prevalent existing deep learning-based approaches provide competitive prediction accuracy, a more interpretable model is desirable to help understand how different features may contribute to CRISPR-Cas9 cleavage efficiency. RESULTS: We propose a gradient boosting approach, utilizing LightGBM to develop an integrated tool, BoostMEC (Boosting Model for Efficient CRISPR), for the prediction of wild-type CRISPR-Cas9 editing efficiency. We benchmark BoostMEC against 10 popular models on 13 external datasets and show its competitive performance. CONCLUSIONS: BoostMEC can provide state-of-the-art predictions of CRISPR-Cas9 cleavage efficiency for sgRNA design and selection. Relying on direct and derived sequence features of sgRNA sequences and based on conventional machine learning, BoostMEC maintains an advantage over other state-of-the-art CRISPR efficiency prediction models that are based on deep learning through its ability to produce more interpretable feature insights and predictions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04998-z.
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spelling pubmed-95979632022-10-27 BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models Zarate, Oscar A. Yang, Yiben Wang, Xiaozhong Wang, Ji-Ping BMC Bioinformatics Research BACKGROUND: In the CRISPR-Cas9 system, the efficiency of genetic modifications has been found to vary depending on the single guide RNA (sgRNA) used. A variety of sgRNA properties have been found to be predictive of CRISPR cleavage efficiency, including the position-specific sequence composition of sgRNAs, global sgRNA sequence properties, and thermodynamic features. While prevalent existing deep learning-based approaches provide competitive prediction accuracy, a more interpretable model is desirable to help understand how different features may contribute to CRISPR-Cas9 cleavage efficiency. RESULTS: We propose a gradient boosting approach, utilizing LightGBM to develop an integrated tool, BoostMEC (Boosting Model for Efficient CRISPR), for the prediction of wild-type CRISPR-Cas9 editing efficiency. We benchmark BoostMEC against 10 popular models on 13 external datasets and show its competitive performance. CONCLUSIONS: BoostMEC can provide state-of-the-art predictions of CRISPR-Cas9 cleavage efficiency for sgRNA design and selection. Relying on direct and derived sequence features of sgRNA sequences and based on conventional machine learning, BoostMEC maintains an advantage over other state-of-the-art CRISPR efficiency prediction models that are based on deep learning through its ability to produce more interpretable feature insights and predictions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04998-z. BioMed Central 2022-10-26 /pmc/articles/PMC9597963/ /pubmed/36289480 http://dx.doi.org/10.1186/s12859-022-04998-z Text en © The Author(s) 2022 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 Research
Zarate, Oscar A.
Yang, Yiben
Wang, Xiaozhong
Wang, Ji-Ping
BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models
title BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models
title_full BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models
title_fullStr BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models
title_full_unstemmed BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models
title_short BoostMEC: predicting CRISPR-Cas9 cleavage efficiency through boosting models
title_sort boostmec: predicting crispr-cas9 cleavage efficiency through boosting models
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597963/
https://www.ncbi.nlm.nih.gov/pubmed/36289480
http://dx.doi.org/10.1186/s12859-022-04998-z
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