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SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost

BACKGROUND: Identifying miRNA and disease associations helps us understand disease mechanisms of action from the molecular level. However, it is usually blind, time-consuming, and small-scale based on biological experiments. Hence, developing computational methods to predict unknown miRNA and diseas...

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Autores principales: Liu, Dayun, Huang, Yibiao, Nie, Wenjuan, Zhang, Jiaxuan, Deng, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082881/
https://www.ncbi.nlm.nih.gov/pubmed/33910505
http://dx.doi.org/10.1186/s12859-021-04135-2
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author Liu, Dayun
Huang, Yibiao
Nie, Wenjuan
Zhang, Jiaxuan
Deng, Lei
author_facet Liu, Dayun
Huang, Yibiao
Nie, Wenjuan
Zhang, Jiaxuan
Deng, Lei
author_sort Liu, Dayun
collection PubMed
description BACKGROUND: Identifying miRNA and disease associations helps us understand disease mechanisms of action from the molecular level. However, it is usually blind, time-consuming, and small-scale based on biological experiments. Hence, developing computational methods to predict unknown miRNA and disease associations is becoming increasingly important. RESULTS: In this work, we develop a computational framework called SMALF to predict unknown miRNA-disease associations. SMALF first utilizes a stacked autoencoder to learn miRNA latent feature and disease latent feature from the original miRNA-disease association matrix. Then, SMALF obtains the feature vector of representing miRNA-disease by integrating miRNA functional similarity, miRNA latent feature, disease semantic similarity, and disease latent feature. Finally, XGBoost is utilized to predict unknown miRNA-disease associations. We implement cross-validation experiments. Compared with other state-of-the-art methods, SAMLF achieved the best AUC value. We also construct three case studies, including hepatocellular carcinoma, colon cancer, and breast cancer. The results show that 10, 10, and 9 out of the top ten predicted miRNAs are verified in MNDR v3.0 or miRCancer, respectively. CONCLUSION: The comprehensive experimental results demonstrate that SMALF is effective in identifying unknown miRNA-disease associations.
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spelling pubmed-80828812021-04-29 SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost Liu, Dayun Huang, Yibiao Nie, Wenjuan Zhang, Jiaxuan Deng, Lei BMC Bioinformatics Research BACKGROUND: Identifying miRNA and disease associations helps us understand disease mechanisms of action from the molecular level. However, it is usually blind, time-consuming, and small-scale based on biological experiments. Hence, developing computational methods to predict unknown miRNA and disease associations is becoming increasingly important. RESULTS: In this work, we develop a computational framework called SMALF to predict unknown miRNA-disease associations. SMALF first utilizes a stacked autoencoder to learn miRNA latent feature and disease latent feature from the original miRNA-disease association matrix. Then, SMALF obtains the feature vector of representing miRNA-disease by integrating miRNA functional similarity, miRNA latent feature, disease semantic similarity, and disease latent feature. Finally, XGBoost is utilized to predict unknown miRNA-disease associations. We implement cross-validation experiments. Compared with other state-of-the-art methods, SAMLF achieved the best AUC value. We also construct three case studies, including hepatocellular carcinoma, colon cancer, and breast cancer. The results show that 10, 10, and 9 out of the top ten predicted miRNAs are verified in MNDR v3.0 or miRCancer, respectively. CONCLUSION: The comprehensive experimental results demonstrate that SMALF is effective in identifying unknown miRNA-disease associations. BioMed Central 2021-04-28 /pmc/articles/PMC8082881/ /pubmed/33910505 http://dx.doi.org/10.1186/s12859-021-04135-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Dayun
Huang, Yibiao
Nie, Wenjuan
Zhang, Jiaxuan
Deng, Lei
SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost
title SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost
title_full SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost
title_fullStr SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost
title_full_unstemmed SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost
title_short SMALF: miRNA-disease associations prediction based on stacked autoencoder and XGBoost
title_sort smalf: mirna-disease associations prediction based on stacked autoencoder and xgboost
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082881/
https://www.ncbi.nlm.nih.gov/pubmed/33910505
http://dx.doi.org/10.1186/s12859-021-04135-2
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