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A disease-related gene mining method based on weakly supervised learning model
BACKGROUND: Predicting disease-related genes is helpful for understanding the disease pathology and the molecular mechanisms during the disease progression. However, traditional methods are not suitable for screening genes related to the disease development, because there are some samples with weak...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886251/ https://www.ncbi.nlm.nih.gov/pubmed/31787083 http://dx.doi.org/10.1186/s12859-019-3078-9 |
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author | Zhang, Han Huo, Xueting Guo, Xia Su, Xin Quan, Xiongwen Jin, Chen |
author_facet | Zhang, Han Huo, Xueting Guo, Xia Su, Xin Quan, Xiongwen Jin, Chen |
author_sort | Zhang, Han |
collection | PubMed |
description | BACKGROUND: Predicting disease-related genes is helpful for understanding the disease pathology and the molecular mechanisms during the disease progression. However, traditional methods are not suitable for screening genes related to the disease development, because there are some samples with weak label information in the disease dataset and a small number of genes are known disease-related genes. RESULTS: We designed a disease-related gene mining method based on the weakly supervised learning model in this paper. The method is separated into two steps. Firstly, the differentially expressed genes are screened based on the weakly supervised learning model. In the model, the strong and weak label information at different stages of the disease progression is fully utilized. The obtained differentially expressed gene set is stable and complete after the algorithm converges. Then, we screen disease-related genes in the obtained differentially expressed gene set using transductive support vector machine based on the difference kernel function. The difference kernel function can map the input space of the original Huntington’s disease gene expression dataset to the difference space. The relation between the two genes can be evaluated more accurately in the difference space and the known disease-related gene information can be used effectively. CONCLUSIONS: The experimental results show that the disease-related gene mining method based on the weakly supervised learning model can effectively improve the precision of the disease-related gene prediction compared with other excellent methods. |
format | Online Article Text |
id | pubmed-6886251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68862512019-12-11 A disease-related gene mining method based on weakly supervised learning model Zhang, Han Huo, Xueting Guo, Xia Su, Xin Quan, Xiongwen Jin, Chen BMC Bioinformatics Research BACKGROUND: Predicting disease-related genes is helpful for understanding the disease pathology and the molecular mechanisms during the disease progression. However, traditional methods are not suitable for screening genes related to the disease development, because there are some samples with weak label information in the disease dataset and a small number of genes are known disease-related genes. RESULTS: We designed a disease-related gene mining method based on the weakly supervised learning model in this paper. The method is separated into two steps. Firstly, the differentially expressed genes are screened based on the weakly supervised learning model. In the model, the strong and weak label information at different stages of the disease progression is fully utilized. The obtained differentially expressed gene set is stable and complete after the algorithm converges. Then, we screen disease-related genes in the obtained differentially expressed gene set using transductive support vector machine based on the difference kernel function. The difference kernel function can map the input space of the original Huntington’s disease gene expression dataset to the difference space. The relation between the two genes can be evaluated more accurately in the difference space and the known disease-related gene information can be used effectively. CONCLUSIONS: The experimental results show that the disease-related gene mining method based on the weakly supervised learning model can effectively improve the precision of the disease-related gene prediction compared with other excellent methods. BioMed Central 2019-12-02 /pmc/articles/PMC6886251/ /pubmed/31787083 http://dx.doi.org/10.1186/s12859-019-3078-9 Text en © The Author(s) 2019 Open Access This 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 Zhang, Han Huo, Xueting Guo, Xia Su, Xin Quan, Xiongwen Jin, Chen A disease-related gene mining method based on weakly supervised learning model |
title | A disease-related gene mining method based on weakly supervised learning model |
title_full | A disease-related gene mining method based on weakly supervised learning model |
title_fullStr | A disease-related gene mining method based on weakly supervised learning model |
title_full_unstemmed | A disease-related gene mining method based on weakly supervised learning model |
title_short | A disease-related gene mining method based on weakly supervised learning model |
title_sort | disease-related gene mining method based on weakly supervised learning model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886251/ https://www.ncbi.nlm.nih.gov/pubmed/31787083 http://dx.doi.org/10.1186/s12859-019-3078-9 |
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