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MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data
MOTIVATION: Screening new drug–target interactions (DTIs) by traditional experimental methods is costly and time-consuming. Recent advances in knowledge graphs, chemical linear notations, and genomic data enable researchers to develop computational-based-DTI models, which play a pivotal role in drug...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10329491/ https://www.ncbi.nlm.nih.gov/pubmed/37379157 http://dx.doi.org/10.1093/bioinformatics/btad411 |
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author | Xia, Xiaoqiong Zhu, Chaoyu Zhong, Fan Liu, Lei |
author_facet | Xia, Xiaoqiong Zhu, Chaoyu Zhong, Fan Liu, Lei |
author_sort | Xia, Xiaoqiong |
collection | PubMed |
description | MOTIVATION: Screening new drug–target interactions (DTIs) by traditional experimental methods is costly and time-consuming. Recent advances in knowledge graphs, chemical linear notations, and genomic data enable researchers to develop computational-based-DTI models, which play a pivotal role in drug repurposing and discovery. However, there still needs to develop a multimodal fusion DTI model that integrates available heterogeneous data into a unified framework. RESULTS: We developed MDTips, a multimodal-data-based DTI prediction system, by fusing the knowledge graphs, gene expression profiles, and structural information of drugs/targets. MDTips yielded accurate and robust performance on DTI predictions. We found that multimodal fusion learning can fully consider the importance of each modality and incorporate information from multiple aspects, thus improving model performance. Extensive experimental results demonstrate that deep learning-based encoders (i.e. Attentive FP and Transformer) outperform traditional chemical descriptors/fingerprints, and MDTips outperforms other state-of-the-art prediction models. MDTips is designed to predict the input drugs’ candidate targets, side effects, and indications with all available modalities. Via MDTips, we reverse-screened candidate targets of 6766 drugs, which can be used for drug repurposing and discovery. AVAILABILITY AND IMPLEMENTATION: https://github.com/XiaoqiongXia/MDTips and https://doi.org/10.5281/zenodo.7560544. |
format | Online Article Text |
id | pubmed-10329491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103294912023-07-09 MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data Xia, Xiaoqiong Zhu, Chaoyu Zhong, Fan Liu, Lei Bioinformatics Original Paper MOTIVATION: Screening new drug–target interactions (DTIs) by traditional experimental methods is costly and time-consuming. Recent advances in knowledge graphs, chemical linear notations, and genomic data enable researchers to develop computational-based-DTI models, which play a pivotal role in drug repurposing and discovery. However, there still needs to develop a multimodal fusion DTI model that integrates available heterogeneous data into a unified framework. RESULTS: We developed MDTips, a multimodal-data-based DTI prediction system, by fusing the knowledge graphs, gene expression profiles, and structural information of drugs/targets. MDTips yielded accurate and robust performance on DTI predictions. We found that multimodal fusion learning can fully consider the importance of each modality and incorporate information from multiple aspects, thus improving model performance. Extensive experimental results demonstrate that deep learning-based encoders (i.e. Attentive FP and Transformer) outperform traditional chemical descriptors/fingerprints, and MDTips outperforms other state-of-the-art prediction models. MDTips is designed to predict the input drugs’ candidate targets, side effects, and indications with all available modalities. Via MDTips, we reverse-screened candidate targets of 6766 drugs, which can be used for drug repurposing and discovery. AVAILABILITY AND IMPLEMENTATION: https://github.com/XiaoqiongXia/MDTips and https://doi.org/10.5281/zenodo.7560544. Oxford University Press 2023-06-28 /pmc/articles/PMC10329491/ /pubmed/37379157 http://dx.doi.org/10.1093/bioinformatics/btad411 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Xia, Xiaoqiong Zhu, Chaoyu Zhong, Fan Liu, Lei MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data |
title | MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data |
title_full | MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data |
title_fullStr | MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data |
title_full_unstemmed | MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data |
title_short | MDTips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data |
title_sort | mdtips: a multimodal-data-based drug–target interaction prediction system fusing knowledge, gene expression profile, and structural data |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10329491/ https://www.ncbi.nlm.nih.gov/pubmed/37379157 http://dx.doi.org/10.1093/bioinformatics/btad411 |
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