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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2021-08-01
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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 |
_version_ |
1721197679703228416 |