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Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning
BACKGROUND: Alzheimer’s disease (AD) is an important, progressive neurodegenerative disease, with a complex genetic architecture. A key goal of biomedical research is to seek out disease risk genes, and to elucidate the function of these risk genes in the development of disease. For this purpose, ex...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763548/ https://www.ncbi.nlm.nih.gov/pubmed/29320986 http://dx.doi.org/10.1186/s12883-017-1010-3 |
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author | Huang, Xiaoyan Liu, Hankui Li, Xinming Guan, Liping Li, Jiankang Tellier, Laurent Christian Asker M. Yang, Huanming Wang, Jian Zhang, Jianguo |
author_facet | Huang, Xiaoyan Liu, Hankui Li, Xinming Guan, Liping Li, Jiankang Tellier, Laurent Christian Asker M. Yang, Huanming Wang, Jian Zhang, Jianguo |
author_sort | Huang, Xiaoyan |
collection | PubMed |
description | BACKGROUND: Alzheimer’s disease (AD) is an important, progressive neurodegenerative disease, with a complex genetic architecture. A key goal of biomedical research is to seek out disease risk genes, and to elucidate the function of these risk genes in the development of disease. For this purpose, expanding the AD-associated gene set is necessary. In past research, the prediction methods for AD related genes has been limited in their exploration of the target genome regions. We here present a genome-wide method for AD candidate genes predictions. METHODS: We present a machine learning approach (SVM), based upon integrating gene expression data with human brain-specific gene network data, to discover the full spectrum of AD genes across the whole genome. RESULTS: We classified AD candidate genes with an accuracy and the area under the receiver operating characteristic (ROC) curve of 84.56% and 94%. Our approach provides a supplement for the spectrum of AD-associated genes extracted from more than 20,000 genes in a genome wide scale. CONCLUSIONS: In this study, we have elucidated the whole-genome spectrum of AD, using a machine learning approach. Through this method, we expect for the candidate gene catalogue to provide a more comprehensive annotation of AD for researchers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12883-017-1010-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5763548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57635482018-01-17 Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning Huang, Xiaoyan Liu, Hankui Li, Xinming Guan, Liping Li, Jiankang Tellier, Laurent Christian Asker M. Yang, Huanming Wang, Jian Zhang, Jianguo BMC Neurol Research Article BACKGROUND: Alzheimer’s disease (AD) is an important, progressive neurodegenerative disease, with a complex genetic architecture. A key goal of biomedical research is to seek out disease risk genes, and to elucidate the function of these risk genes in the development of disease. For this purpose, expanding the AD-associated gene set is necessary. In past research, the prediction methods for AD related genes has been limited in their exploration of the target genome regions. We here present a genome-wide method for AD candidate genes predictions. METHODS: We present a machine learning approach (SVM), based upon integrating gene expression data with human brain-specific gene network data, to discover the full spectrum of AD genes across the whole genome. RESULTS: We classified AD candidate genes with an accuracy and the area under the receiver operating characteristic (ROC) curve of 84.56% and 94%. Our approach provides a supplement for the spectrum of AD-associated genes extracted from more than 20,000 genes in a genome wide scale. CONCLUSIONS: In this study, we have elucidated the whole-genome spectrum of AD, using a machine learning approach. Through this method, we expect for the candidate gene catalogue to provide a more comprehensive annotation of AD for researchers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12883-017-1010-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-10 /pmc/articles/PMC5763548/ /pubmed/29320986 http://dx.doi.org/10.1186/s12883-017-1010-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Huang, Xiaoyan Liu, Hankui Li, Xinming Guan, Liping Li, Jiankang Tellier, Laurent Christian Asker M. Yang, Huanming Wang, Jian Zhang, Jianguo Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning |
title | Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning |
title_full | Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning |
title_fullStr | Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning |
title_full_unstemmed | Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning |
title_short | Revealing Alzheimer’s disease genes spectrum in the whole-genome by machine learning |
title_sort | revealing alzheimer’s disease genes spectrum in the whole-genome by machine learning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763548/ https://www.ncbi.nlm.nih.gov/pubmed/29320986 http://dx.doi.org/10.1186/s12883-017-1010-3 |
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