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DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome

Despite great advances, molecular cancer pathology is often limited to the use of a small number of biomarkers rather than the whole transcriptome, partly due to computational challenges. Here, we introduce a novel architecture of Deep Neural Networks (DNNs) that is capable of simultaneous inference...

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Autores principales: Azarkhalili, Behrooz, Saberi, Ali, Chitsaz, Hamidreza, Sharifi-Zarchi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848155/
https://www.ncbi.nlm.nih.gov/pubmed/31712594
http://dx.doi.org/10.1038/s41598-019-52937-5
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author Azarkhalili, Behrooz
Saberi, Ali
Chitsaz, Hamidreza
Sharifi-Zarchi, Ali
author_facet Azarkhalili, Behrooz
Saberi, Ali
Chitsaz, Hamidreza
Sharifi-Zarchi, Ali
author_sort Azarkhalili, Behrooz
collection PubMed
description Despite great advances, molecular cancer pathology is often limited to the use of a small number of biomarkers rather than the whole transcriptome, partly due to computational challenges. Here, we introduce a novel architecture of Deep Neural Networks (DNNs) that is capable of simultaneous inference of various properties of biological samples, through multi-task and transfer learning. It encodes the whole transcription profile into a strikingly low-dimensional latent vector of size 8, and then recovers mRNA and miRNA expression profiles, tissue and disease type from this vector. This latent space is significantly better than the original gene expression profiles for discriminating samples based on their tissue and disease. We employed this architecture on mRNA transcription profiles of 10750 clinical samples from 34 classes (one healthy and 33 different types of cancer) from 27 tissues. Our method significantly outperforms prior works and classical machine learning approaches in predicting tissue-of-origin, normal or disease state and cancer type of each sample. For tissues with more than one type of cancer, it reaches 99.4% accuracy in identifying the correct cancer subtype. We also show this system is very robust against noise and missing values. Collectively, our results highlight applications of artificial intelligence in molecular cancer pathology and oncological research. DeePathology is freely available at https://github.com/SharifBioinf/DeePathology.
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spelling pubmed-68481552019-11-19 DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome Azarkhalili, Behrooz Saberi, Ali Chitsaz, Hamidreza Sharifi-Zarchi, Ali Sci Rep Article Despite great advances, molecular cancer pathology is often limited to the use of a small number of biomarkers rather than the whole transcriptome, partly due to computational challenges. Here, we introduce a novel architecture of Deep Neural Networks (DNNs) that is capable of simultaneous inference of various properties of biological samples, through multi-task and transfer learning. It encodes the whole transcription profile into a strikingly low-dimensional latent vector of size 8, and then recovers mRNA and miRNA expression profiles, tissue and disease type from this vector. This latent space is significantly better than the original gene expression profiles for discriminating samples based on their tissue and disease. We employed this architecture on mRNA transcription profiles of 10750 clinical samples from 34 classes (one healthy and 33 different types of cancer) from 27 tissues. Our method significantly outperforms prior works and classical machine learning approaches in predicting tissue-of-origin, normal or disease state and cancer type of each sample. For tissues with more than one type of cancer, it reaches 99.4% accuracy in identifying the correct cancer subtype. We also show this system is very robust against noise and missing values. Collectively, our results highlight applications of artificial intelligence in molecular cancer pathology and oncological research. DeePathology is freely available at https://github.com/SharifBioinf/DeePathology. Nature Publishing Group UK 2019-11-11 /pmc/articles/PMC6848155/ /pubmed/31712594 http://dx.doi.org/10.1038/s41598-019-52937-5 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Azarkhalili, Behrooz
Saberi, Ali
Chitsaz, Hamidreza
Sharifi-Zarchi, Ali
DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome
title DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome
title_full DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome
title_fullStr DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome
title_full_unstemmed DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome
title_short DeePathology: Deep Multi-Task Learning for Inferring Molecular Pathology from Cancer Transcriptome
title_sort deepathology: deep multi-task learning for inferring molecular pathology from cancer transcriptome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848155/
https://www.ncbi.nlm.nih.gov/pubmed/31712594
http://dx.doi.org/10.1038/s41598-019-52937-5
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