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VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder
MOTIVATION: Accurate identification of Drug-Target Interactions (DTIs) plays a crucial role in many stages of drug development and drug repurposing. (i) Traditional methods do not consider the use of multi-source data and do not consider the complex relationship between data sources. (ii) How to bet...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324201/ https://www.ncbi.nlm.nih.gov/pubmed/37415176 http://dx.doi.org/10.1186/s12859-023-05387-w |
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author | Zhang, Yuanyuan Feng, Yinfei Wu, Mengjie Deng, Zengqian Wang, Shudong |
author_facet | Zhang, Yuanyuan Feng, Yinfei Wu, Mengjie Deng, Zengqian Wang, Shudong |
author_sort | Zhang, Yuanyuan |
collection | PubMed |
description | MOTIVATION: Accurate identification of Drug-Target Interactions (DTIs) plays a crucial role in many stages of drug development and drug repurposing. (i) Traditional methods do not consider the use of multi-source data and do not consider the complex relationship between data sources. (ii) How to better mine the hidden features of drug and target space from high-dimensional data, and better solve the accuracy and robustness of the model. RESULTS: To solve the above problems, a novel prediction model named VGAEDTI is proposed in this paper. We constructed a heterogeneous network with multiple sources of information using multiple types of drug and target dataIn order to obtain deeper features of drugs and targets, we use two different autoencoders. One is variational graph autoencoder (VGAE) which is used to infer feature representations from drug and target spaces. The second is graph autoencoder (GAE) propagating labels between known DTIs. Experimental results on two public datasets show that the prediction accuracy of VGAEDTI is better than that of six DTIs prediction methods. These results indicate that model can predict new DTIs and provide an effective tool for accelerating drug development and repurposing. |
format | Online Article Text |
id | pubmed-10324201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103242012023-07-07 VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder Zhang, Yuanyuan Feng, Yinfei Wu, Mengjie Deng, Zengqian Wang, Shudong BMC Bioinformatics Research MOTIVATION: Accurate identification of Drug-Target Interactions (DTIs) plays a crucial role in many stages of drug development and drug repurposing. (i) Traditional methods do not consider the use of multi-source data and do not consider the complex relationship between data sources. (ii) How to better mine the hidden features of drug and target space from high-dimensional data, and better solve the accuracy and robustness of the model. RESULTS: To solve the above problems, a novel prediction model named VGAEDTI is proposed in this paper. We constructed a heterogeneous network with multiple sources of information using multiple types of drug and target dataIn order to obtain deeper features of drugs and targets, we use two different autoencoders. One is variational graph autoencoder (VGAE) which is used to infer feature representations from drug and target spaces. The second is graph autoencoder (GAE) propagating labels between known DTIs. Experimental results on two public datasets show that the prediction accuracy of VGAEDTI is better than that of six DTIs prediction methods. These results indicate that model can predict new DTIs and provide an effective tool for accelerating drug development and repurposing. BioMed Central 2023-07-06 /pmc/articles/PMC10324201/ /pubmed/37415176 http://dx.doi.org/10.1186/s12859-023-05387-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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 Zhang, Yuanyuan Feng, Yinfei Wu, Mengjie Deng, Zengqian Wang, Shudong VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder |
title | VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder |
title_full | VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder |
title_fullStr | VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder |
title_full_unstemmed | VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder |
title_short | VGAEDTI: drug-target interaction prediction based on variational inference and graph autoencoder |
title_sort | vgaedti: drug-target interaction prediction based on variational inference and graph autoencoder |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324201/ https://www.ncbi.nlm.nih.gov/pubmed/37415176 http://dx.doi.org/10.1186/s12859-023-05387-w |
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