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i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability
Effective and precise classification of glioma patients for their disease risks is critical to improving early diagnosis and patient survival. In the recent past, a significant amount of multi-omics data derived from cancer patients has emerged. However, a robust framework for integrating multi-omic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284388/ https://www.ncbi.nlm.nih.gov/pubmed/35860408 http://dx.doi.org/10.1016/j.csbj.2022.06.058 |
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author | Pan, Xingxin Burgman, Brandon Wu, Erxi Huang, Jason H. Sahni, Nidhi Stephen Yi, S. |
author_facet | Pan, Xingxin Burgman, Brandon Wu, Erxi Huang, Jason H. Sahni, Nidhi Stephen Yi, S. |
author_sort | Pan, Xingxin |
collection | PubMed |
description | Effective and precise classification of glioma patients for their disease risks is critical to improving early diagnosis and patient survival. In the recent past, a significant amount of multi-omics data derived from cancer patients has emerged. However, a robust framework for integrating multi-omics data types to efficiently and precisely subgroup glioma patients and predict survival prognosis is still lacking. In addition, effective therapeutic targets for treating glioma patients with poor prognoses are in dire need. To begin to resolve this difficulty, we developed i-Modern, an integrated Multi-omics deep learning network method, and optimized a sophisticated computational model in gliomas that can accurately stratify patients based on their prognosis. We built a survival-associated predictive framework integrating transcription profile, miRNA expression, somatic mutations, copy number variation (CNV), DNA methylation, and protein expression. This framework achieved promising performance in distinguishing high-risk glioma patients from those with good prognoses. Furthermore, we constructed multiple fully connected neural networks that are trained on prioritized multi-omics signatures or even only potential single-omics signatures, based on our customized scoring system. Together, the landmark multi-omics signatures we identified may serve as potential therapeutic targets in gliomas. |
format | Online Article Text |
id | pubmed-9284388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92843882022-07-19 i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability Pan, Xingxin Burgman, Brandon Wu, Erxi Huang, Jason H. Sahni, Nidhi Stephen Yi, S. Comput Struct Biotechnol J Research Article Effective and precise classification of glioma patients for their disease risks is critical to improving early diagnosis and patient survival. In the recent past, a significant amount of multi-omics data derived from cancer patients has emerged. However, a robust framework for integrating multi-omics data types to efficiently and precisely subgroup glioma patients and predict survival prognosis is still lacking. In addition, effective therapeutic targets for treating glioma patients with poor prognoses are in dire need. To begin to resolve this difficulty, we developed i-Modern, an integrated Multi-omics deep learning network method, and optimized a sophisticated computational model in gliomas that can accurately stratify patients based on their prognosis. We built a survival-associated predictive framework integrating transcription profile, miRNA expression, somatic mutations, copy number variation (CNV), DNA methylation, and protein expression. This framework achieved promising performance in distinguishing high-risk glioma patients from those with good prognoses. Furthermore, we constructed multiple fully connected neural networks that are trained on prioritized multi-omics signatures or even only potential single-omics signatures, based on our customized scoring system. Together, the landmark multi-omics signatures we identified may serve as potential therapeutic targets in gliomas. Research Network of Computational and Structural Biotechnology 2022-06-30 /pmc/articles/PMC9284388/ /pubmed/35860408 http://dx.doi.org/10.1016/j.csbj.2022.06.058 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Pan, Xingxin Burgman, Brandon Wu, Erxi Huang, Jason H. Sahni, Nidhi Stephen Yi, S. i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability |
title | i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability |
title_full | i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability |
title_fullStr | i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability |
title_full_unstemmed | i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability |
title_short | i-Modern: Integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability |
title_sort | i-modern: integrated multi-omics network model identifies potential therapeutic targets in glioma by deep learning with interpretability |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284388/ https://www.ncbi.nlm.nih.gov/pubmed/35860408 http://dx.doi.org/10.1016/j.csbj.2022.06.058 |
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