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Using deep learning to associate human genes with age-related diseases

MOTIVATION: One way to identify genes possibly associated with ageing is to build a classification model (from the machine learning field) capable of classifying genes as associated with multiple age-related diseases. To build this model, we use a pre-compiled list of human genes associated with age...

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Detalles Bibliográficos
Autores principales: Fabris, Fabio, Palmer, Daniel, Salama, Khalid M, de Magalhães, João Pedro, Freitas, Alex A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141856/
https://www.ncbi.nlm.nih.gov/pubmed/31845988
http://dx.doi.org/10.1093/bioinformatics/btz887
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author Fabris, Fabio
Palmer, Daniel
Salama, Khalid M
de Magalhães, João Pedro
Freitas, Alex A
author_facet Fabris, Fabio
Palmer, Daniel
Salama, Khalid M
de Magalhães, João Pedro
Freitas, Alex A
author_sort Fabris, Fabio
collection PubMed
description MOTIVATION: One way to identify genes possibly associated with ageing is to build a classification model (from the machine learning field) capable of classifying genes as associated with multiple age-related diseases. To build this model, we use a pre-compiled list of human genes associated with age-related diseases and apply a novel Deep Neural Network (DNN) method to find associations between gene descriptors (e.g. Gene Ontology terms, protein–protein interaction data and biological pathway information) and age-related diseases. RESULTS: The novelty of our new DNN method is its modular architecture, which has the capability of combining several sources of biological data to predict which ageing-related diseases a gene is associated with (if any). Our DNN method achieves better predictive performance than standard DNN approaches, a Gradient Boosted Tree classifier (a strong baseline method) and a Logistic Regression classifier. Given the DNN model produced by our method, we use two approaches to identify human genes that are not known to be associated with age-related diseases according to our dataset. First, we investigate genes that are close to other disease-associated genes in a complex multi-dimensional feature space learned by the DNN algorithm. Second, using the class label probabilities output by our DNN approach, we identify genes with a high probability of being associated with age-related diseases according to the model. We provide evidence of these putative associations retrieved from the DNN model with literature support. AVAILABILITY AND IMPLEMENTATION: The source code and datasets can be found at: https://github.com/fabiofabris/Bioinfo2019. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-71418562020-04-13 Using deep learning to associate human genes with age-related diseases Fabris, Fabio Palmer, Daniel Salama, Khalid M de Magalhães, João Pedro Freitas, Alex A Bioinformatics Original Papers MOTIVATION: One way to identify genes possibly associated with ageing is to build a classification model (from the machine learning field) capable of classifying genes as associated with multiple age-related diseases. To build this model, we use a pre-compiled list of human genes associated with age-related diseases and apply a novel Deep Neural Network (DNN) method to find associations between gene descriptors (e.g. Gene Ontology terms, protein–protein interaction data and biological pathway information) and age-related diseases. RESULTS: The novelty of our new DNN method is its modular architecture, which has the capability of combining several sources of biological data to predict which ageing-related diseases a gene is associated with (if any). Our DNN method achieves better predictive performance than standard DNN approaches, a Gradient Boosted Tree classifier (a strong baseline method) and a Logistic Regression classifier. Given the DNN model produced by our method, we use two approaches to identify human genes that are not known to be associated with age-related diseases according to our dataset. First, we investigate genes that are close to other disease-associated genes in a complex multi-dimensional feature space learned by the DNN algorithm. Second, using the class label probabilities output by our DNN approach, we identify genes with a high probability of being associated with age-related diseases according to the model. We provide evidence of these putative associations retrieved from the DNN model with literature support. AVAILABILITY AND IMPLEMENTATION: The source code and datasets can be found at: https://github.com/fabiofabris/Bioinfo2019. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2020-04-01 2019-12-17 /pmc/articles/PMC7141856/ /pubmed/31845988 http://dx.doi.org/10.1093/bioinformatics/btz887 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Fabris, Fabio
Palmer, Daniel
Salama, Khalid M
de Magalhães, João Pedro
Freitas, Alex A
Using deep learning to associate human genes with age-related diseases
title Using deep learning to associate human genes with age-related diseases
title_full Using deep learning to associate human genes with age-related diseases
title_fullStr Using deep learning to associate human genes with age-related diseases
title_full_unstemmed Using deep learning to associate human genes with age-related diseases
title_short Using deep learning to associate human genes with age-related diseases
title_sort using deep learning to associate human genes with age-related diseases
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141856/
https://www.ncbi.nlm.nih.gov/pubmed/31845988
http://dx.doi.org/10.1093/bioinformatics/btz887
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