Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction Prediction

Drug repositioning is a method of systematically identifying potential molecular targets that known drugs may act on. Compared with traditional methods, drug repositioning has been extensively studied due to the development of multi-omics technology and system biology methods. Because of its biologi...

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Main Authors: Ying Zheng, Zheng Wu
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.702259/full
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spelling doaj-40d10ed05535495c93a580d18f1df83b2021-08-24T09:54:58ZengFrontiers Media S.A.Frontiers in Genetics1664-80212021-08-011210.3389/fgene.2021.702259702259Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction PredictionYing ZhengZheng WuDrug repositioning is a method of systematically identifying potential molecular targets that known drugs may act on. Compared with traditional methods, drug repositioning has been extensively studied due to the development of multi-omics technology and system biology methods. Because of its biological network properties, it is possible to apply machine learning related algorithms for prediction. Based on various heterogeneous network model, this paper proposes a method named THNCDF for predicting drug–target interactions. Various heterogeneous networks are integrated to build a tripartite network, and similarity calculation methods are used to obtain similarity matrix. Then, the cascade deep forest method is used to make prediction. Results indicate that THNCDF outperforms the previously reported methods based on the 10-fold cross-validation on the benchmark data sets proposed by Y. Yamanishi. The area under Precision Recall curve (AUPR) value on the Enzyme, GPCR, Ion Channel, and Nuclear Receptor data sets is 0.988, 0.980, 0.938, and 0.906 separately. The experimental results well illustrate the feasibility of this method.https://www.frontiersin.org/articles/10.3389/fgene.2021.702259/fulldrug repositioningdrug discoverydrug–target interactionheterogeneous similarity measurescascade deep forest
collection DOAJ
language English
format Article
sources DOAJ
author Ying Zheng
Zheng Wu
spellingShingle Ying Zheng
Zheng Wu
Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction Prediction
Frontiers in Genetics
drug repositioning
drug discovery
drug–target interaction
heterogeneous similarity measures
cascade deep forest
author_facet Ying Zheng
Zheng Wu
author_sort Ying Zheng
title Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction Prediction
title_short Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction Prediction
title_full Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction Prediction
title_fullStr Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction Prediction
title_full_unstemmed Cascade Deep Forest With Heterogeneous Similarity Measures for Drug–Target Interaction Prediction
title_sort cascade deep forest with heterogeneous similarity measures for drug–target interaction prediction
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2021-08-01
description Drug repositioning is a method of systematically identifying potential molecular targets that known drugs may act on. Compared with traditional methods, drug repositioning has been extensively studied due to the development of multi-omics technology and system biology methods. Because of its biological network properties, it is possible to apply machine learning related algorithms for prediction. Based on various heterogeneous network model, this paper proposes a method named THNCDF for predicting drug–target interactions. Various heterogeneous networks are integrated to build a tripartite network, and similarity calculation methods are used to obtain similarity matrix. Then, the cascade deep forest method is used to make prediction. Results indicate that THNCDF outperforms the previously reported methods based on the 10-fold cross-validation on the benchmark data sets proposed by Y. Yamanishi. The area under Precision Recall curve (AUPR) value on the Enzyme, GPCR, Ion Channel, and Nuclear Receptor data sets is 0.988, 0.980, 0.938, and 0.906 separately. The experimental results well illustrate the feasibility of this method.
topic drug repositioning
drug discovery
drug–target interaction
heterogeneous similarity measures
cascade deep forest
url https://www.frontiersin.org/articles/10.3389/fgene.2021.702259/full
work_keys_str_mv AT yingzheng cascadedeepforestwithheterogeneoussimilaritymeasuresfordrugtargetinteractionprediction
AT zhengwu cascadedeepforestwithheterogeneoussimilaritymeasuresfordrugtargetinteractionprediction
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