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LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction

An increasing number of evidences indicate microbes are implicated in human physiological mechanisms, including complicated disease pathology. Some microbes have been demonstrated to be associated with diverse important human diseases or disorders. Through investigating these disease-related microbe...

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Detalles Bibliográficos
Autores principales: Wang, Fan, Huang, Zhi-An, Chen, Xing, Zhu, Zexuan, Wen, Zhenkun, Zhao, Jiyun, Yan, Gui-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548838/
https://www.ncbi.nlm.nih.gov/pubmed/28790448
http://dx.doi.org/10.1038/s41598-017-08127-2
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author Wang, Fan
Huang, Zhi-An
Chen, Xing
Zhu, Zexuan
Wen, Zhenkun
Zhao, Jiyun
Yan, Gui-Ying
author_facet Wang, Fan
Huang, Zhi-An
Chen, Xing
Zhu, Zexuan
Wen, Zhenkun
Zhao, Jiyun
Yan, Gui-Ying
author_sort Wang, Fan
collection PubMed
description An increasing number of evidences indicate microbes are implicated in human physiological mechanisms, including complicated disease pathology. Some microbes have been demonstrated to be associated with diverse important human diseases or disorders. Through investigating these disease-related microbes, we can obtain a better understanding of human disease mechanisms for advancing medical scientific progress in terms of disease diagnosis, treatment, prevention, prognosis and drug discovery. Based on the known microbe-disease association network, we developed a semi-supervised computational model of Laplacian Regularized Least Squares for Human Microbe–Disease Association (LRLSHMDA) by introducing Gaussian interaction profile kernel similarity calculation and Laplacian regularized least squares classifier. LRLSHMDA reached the reliable AUCs of 0.8909 and 0.7657 based on the global and local leave-one-out cross validations, respectively. In the framework of 5-fold cross validation, average AUC value of 0.8794 +/−0.0029 further demonstrated its promising prediction ability. In case studies, 9, 9 and 8 of top-10 predicted microbes have been manually certified to be associated with asthma, colorectal carcinoma and chronic obstructive pulmonary disease by published literature evidence. Our proposed model achieves better prediction performance relative to the previous model. We expect that LRLSHMDA could offer insights into identifying more promising human microbe-disease associations in the future.
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spelling pubmed-55488382017-08-09 LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction Wang, Fan Huang, Zhi-An Chen, Xing Zhu, Zexuan Wen, Zhenkun Zhao, Jiyun Yan, Gui-Ying Sci Rep Article An increasing number of evidences indicate microbes are implicated in human physiological mechanisms, including complicated disease pathology. Some microbes have been demonstrated to be associated with diverse important human diseases or disorders. Through investigating these disease-related microbes, we can obtain a better understanding of human disease mechanisms for advancing medical scientific progress in terms of disease diagnosis, treatment, prevention, prognosis and drug discovery. Based on the known microbe-disease association network, we developed a semi-supervised computational model of Laplacian Regularized Least Squares for Human Microbe–Disease Association (LRLSHMDA) by introducing Gaussian interaction profile kernel similarity calculation and Laplacian regularized least squares classifier. LRLSHMDA reached the reliable AUCs of 0.8909 and 0.7657 based on the global and local leave-one-out cross validations, respectively. In the framework of 5-fold cross validation, average AUC value of 0.8794 +/−0.0029 further demonstrated its promising prediction ability. In case studies, 9, 9 and 8 of top-10 predicted microbes have been manually certified to be associated with asthma, colorectal carcinoma and chronic obstructive pulmonary disease by published literature evidence. Our proposed model achieves better prediction performance relative to the previous model. We expect that LRLSHMDA could offer insights into identifying more promising human microbe-disease associations in the future. Nature Publishing Group UK 2017-08-08 /pmc/articles/PMC5548838/ /pubmed/28790448 http://dx.doi.org/10.1038/s41598-017-08127-2 Text en © The Author(s) 2017 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
Wang, Fan
Huang, Zhi-An
Chen, Xing
Zhu, Zexuan
Wen, Zhenkun
Zhao, Jiyun
Yan, Gui-Ying
LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction
title LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction
title_full LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction
title_fullStr LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction
title_full_unstemmed LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction
title_short LRLSHMDA: Laplacian Regularized Least Squares for Human Microbe–Disease Association prediction
title_sort lrlshmda: laplacian regularized least squares for human microbe–disease association prediction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548838/
https://www.ncbi.nlm.nih.gov/pubmed/28790448
http://dx.doi.org/10.1038/s41598-017-08127-2
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