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Predicting gene knockout effects from expression data
BACKGROUND: The study of gene essentiality, which measures the importance of a gene for cell division and survival, is used for the identification of cancer drug targets and understanding of tissue-specific manifestation of genetic conditions. In this work, we analyze essentiality and gene expressio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938619/ https://www.ncbi.nlm.nih.gov/pubmed/36803845 http://dx.doi.org/10.1186/s12920-023-01446-6 |
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author | Rosenski, Jonathan Shifman, Sagiv Kaplan, Tommy |
author_facet | Rosenski, Jonathan Shifman, Sagiv Kaplan, Tommy |
author_sort | Rosenski, Jonathan |
collection | PubMed |
description | BACKGROUND: The study of gene essentiality, which measures the importance of a gene for cell division and survival, is used for the identification of cancer drug targets and understanding of tissue-specific manifestation of genetic conditions. In this work, we analyze essentiality and gene expression data from over 900 cancer lines from the DepMap project to create predictive models of gene essentiality. METHODS: We developed machine learning algorithms to identify those genes whose essentiality levels are explained by the expression of a small set of “modifier genes”. To identify these gene sets, we developed an ensemble of statistical tests capturing linear and non-linear dependencies. We trained several regression models predicting the essentiality of each target gene, and used an automated model selection procedure to identify the optimal model and hyperparameters. Overall, we examined linear models, gradient boosted trees, Gaussian process regression models, and deep learning networks. RESULTS: We identified nearly 3000 genes for which we accurately predict essentiality using gene expression data of a small set of modifier genes. We show that both in the number of genes we successfully make predictions for, as well as in the prediction accuracy, our model outperforms current state-of-the-art works. CONCLUSIONS: Our modeling framework avoids overfitting by identifying the small set of modifier genes, which are of clinical and genetic importance, and ignores the expression of noisy and irrelevant genes. Doing so improves the accuracy of essentiality prediction in various conditions and provides interpretable models. Overall, we present an accurate computational approach, as well as interpretable modeling of essentiality in a wide range of cellular conditions, thus contributing to a better understanding of the molecular mechanisms that govern tissue-specific effects of genetic disease and cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01446-6. |
format | Online Article Text |
id | pubmed-9938619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99386192023-02-19 Predicting gene knockout effects from expression data Rosenski, Jonathan Shifman, Sagiv Kaplan, Tommy BMC Med Genomics Research BACKGROUND: The study of gene essentiality, which measures the importance of a gene for cell division and survival, is used for the identification of cancer drug targets and understanding of tissue-specific manifestation of genetic conditions. In this work, we analyze essentiality and gene expression data from over 900 cancer lines from the DepMap project to create predictive models of gene essentiality. METHODS: We developed machine learning algorithms to identify those genes whose essentiality levels are explained by the expression of a small set of “modifier genes”. To identify these gene sets, we developed an ensemble of statistical tests capturing linear and non-linear dependencies. We trained several regression models predicting the essentiality of each target gene, and used an automated model selection procedure to identify the optimal model and hyperparameters. Overall, we examined linear models, gradient boosted trees, Gaussian process regression models, and deep learning networks. RESULTS: We identified nearly 3000 genes for which we accurately predict essentiality using gene expression data of a small set of modifier genes. We show that both in the number of genes we successfully make predictions for, as well as in the prediction accuracy, our model outperforms current state-of-the-art works. CONCLUSIONS: Our modeling framework avoids overfitting by identifying the small set of modifier genes, which are of clinical and genetic importance, and ignores the expression of noisy and irrelevant genes. Doing so improves the accuracy of essentiality prediction in various conditions and provides interpretable models. Overall, we present an accurate computational approach, as well as interpretable modeling of essentiality in a wide range of cellular conditions, thus contributing to a better understanding of the molecular mechanisms that govern tissue-specific effects of genetic disease and cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01446-6. BioMed Central 2023-02-18 /pmc/articles/PMC9938619/ /pubmed/36803845 http://dx.doi.org/10.1186/s12920-023-01446-6 Text en © The Author(s) 2023 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 Rosenski, Jonathan Shifman, Sagiv Kaplan, Tommy Predicting gene knockout effects from expression data |
title | Predicting gene knockout effects from expression data |
title_full | Predicting gene knockout effects from expression data |
title_fullStr | Predicting gene knockout effects from expression data |
title_full_unstemmed | Predicting gene knockout effects from expression data |
title_short | Predicting gene knockout effects from expression data |
title_sort | predicting gene knockout effects from expression data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938619/ https://www.ncbi.nlm.nih.gov/pubmed/36803845 http://dx.doi.org/10.1186/s12920-023-01446-6 |
work_keys_str_mv | AT rosenskijonathan predictinggeneknockouteffectsfromexpressiondata AT shifmansagiv predictinggeneknockouteffectsfromexpressiondata AT kaplantommy predictinggeneknockouteffectsfromexpressiondata |