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DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies
Although rapid progress has been made in computational approaches for prioritizing cancer driver genes, research is far from achieving the ultimate goal of discovering a complete catalog of genes truly associated with cancer. Driver gene lists predicted from these computational tools lack consistenc...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486576/ https://www.ncbi.nlm.nih.gov/pubmed/30773592 http://dx.doi.org/10.1093/nar/gkz096 |
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author | Han, Yi Yang, Juze Qian, Xinyi Cheng, Wei-Chung Liu, Shu-Hsuan Hua, Xing Zhou, Liyuan Yang, Yaning Wu, Qingbiao Liu, Pengyuan Lu, Yan |
author_facet | Han, Yi Yang, Juze Qian, Xinyi Cheng, Wei-Chung Liu, Shu-Hsuan Hua, Xing Zhou, Liyuan Yang, Yaning Wu, Qingbiao Liu, Pengyuan Lu, Yan |
author_sort | Han, Yi |
collection | PubMed |
description | Although rapid progress has been made in computational approaches for prioritizing cancer driver genes, research is far from achieving the ultimate goal of discovering a complete catalog of genes truly associated with cancer. Driver gene lists predicted from these computational tools lack consistency and are prone to false positives. Here, we developed an approach (DriverML) integrating Rao’s score test and supervised machine learning to identify cancer driver genes. The weight parameters in the score statistics quantified the functional impacts of mutations on the protein. To obtain optimized weight parameters, the score statistics of prior driver genes were maximized on pan-cancer training data. We conducted rigorous and unbiased benchmark analysis and comparisons of DriverML with 20 other existing tools in 31 independent datasets from The Cancer Genome Atlas (TCGA). Our comprehensive evaluations demonstrated that DriverML was robust and powerful among various datasets and outperformed the other tools with a better balance of precision and sensitivity. In vitro cell-based assays further proved the validity of the DriverML prediction of novel driver genes. In summary, DriverML uses an innovative, machine learning-based approach to prioritize cancer driver genes and provides dramatic improvements over currently existing methods. Its source code is available at https://github.com/HelloYiHan/DriverML. |
format | Online Article Text |
id | pubmed-6486576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64865762019-05-01 DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies Han, Yi Yang, Juze Qian, Xinyi Cheng, Wei-Chung Liu, Shu-Hsuan Hua, Xing Zhou, Liyuan Yang, Yaning Wu, Qingbiao Liu, Pengyuan Lu, Yan Nucleic Acids Res Methods Online Although rapid progress has been made in computational approaches for prioritizing cancer driver genes, research is far from achieving the ultimate goal of discovering a complete catalog of genes truly associated with cancer. Driver gene lists predicted from these computational tools lack consistency and are prone to false positives. Here, we developed an approach (DriverML) integrating Rao’s score test and supervised machine learning to identify cancer driver genes. The weight parameters in the score statistics quantified the functional impacts of mutations on the protein. To obtain optimized weight parameters, the score statistics of prior driver genes were maximized on pan-cancer training data. We conducted rigorous and unbiased benchmark analysis and comparisons of DriverML with 20 other existing tools in 31 independent datasets from The Cancer Genome Atlas (TCGA). Our comprehensive evaluations demonstrated that DriverML was robust and powerful among various datasets and outperformed the other tools with a better balance of precision and sensitivity. In vitro cell-based assays further proved the validity of the DriverML prediction of novel driver genes. In summary, DriverML uses an innovative, machine learning-based approach to prioritize cancer driver genes and provides dramatic improvements over currently existing methods. Its source code is available at https://github.com/HelloYiHan/DriverML. Oxford University Press 2019-05-07 2019-02-18 /pmc/articles/PMC6486576/ /pubmed/30773592 http://dx.doi.org/10.1093/nar/gkz096 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Han, Yi Yang, Juze Qian, Xinyi Cheng, Wei-Chung Liu, Shu-Hsuan Hua, Xing Zhou, Liyuan Yang, Yaning Wu, Qingbiao Liu, Pengyuan Lu, Yan DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies |
title | DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies |
title_full | DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies |
title_fullStr | DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies |
title_full_unstemmed | DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies |
title_short | DriverML: a machine learning algorithm for identifying driver genes in cancer sequencing studies |
title_sort | driverml: a machine learning algorithm for identifying driver genes in cancer sequencing studies |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486576/ https://www.ncbi.nlm.nih.gov/pubmed/30773592 http://dx.doi.org/10.1093/nar/gkz096 |
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