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이세민

Lee, Semin
Computational Biology Lab.
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dc.citation.number 1 -
dc.citation.startPage bbac504 -
dc.citation.title BRIEFINGS IN BIOINFORMATICS -
dc.citation.volume 24 -
dc.contributor.author Lee, Kanggeun -
dc.contributor.author Cho, Dongbin -
dc.contributor.author Jang, Jinho -
dc.contributor.author Choi, Kang -
dc.contributor.author Jeong, Hyoung-oh -
dc.contributor.author Seo, Jiwon -
dc.contributor.author Jeong, Won-Ki -
dc.contributor.author Lee, Semin -
dc.date.accessioned 2023-12-21T13:10:04Z -
dc.date.available 2023-12-21T13:10:04Z -
dc.date.created 2022-12-08 -
dc.date.issued 2023-01 -
dc.description.abstract The accurate prediction of cancer drug sensitivity according to the multiomics profiles of individual patients is crucial for precision cancer medicine. However, the development of prediction models has been challenged by the complex crosstalk of input features and the resistance-dominant drug response information contained in public databases. In this study, we propose a novel multidrug response prediction framework, response-aware multitask prediction (RAMP), via a Bayesian neural network and restrict it by soft-supervised contrastive regularization. To utilize network embedding vectors as representation learning features for heterogeneous networks, we harness response-aware negative sampling, which applies cell line–drug response information to the training of network embeddings. RAMP overcomes the prediction accuracy limitation induced by the imbalance of trained response data based on the comprehensive selection and utilization of drug response features. When trained on the Genomics of Drug Sensitivity in Cancer dataset, RAMP achieved an area under the receiver operating characteristic curve > 89%, an area under the precision-recall curve > 59% and an F1 score > 52% and outperformed previously developed methods on both balanced and imbalanced datasets. Furthermore, RAMP predicted many missing drug responses that were not included in the public databases. Our results showed that RAMP will be suitable for the high-throughput prediction of cancer drug sensitivity and will be useful for guiding cancer drug selection processes. The Python implementation for RAMP is available at https://github.com/hvcl/RAMP. -
dc.identifier.bibliographicCitation BRIEFINGS IN BIOINFORMATICS, v.24, no.1, pp.bbac504 -
dc.identifier.doi 10.1093/bib/bbac504 -
dc.identifier.issn 1467-5463 -
dc.identifier.scopusid 2-s2.0-85168141621 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/60076 -
dc.identifier.wosid 000912736500001 -
dc.language 영어 -
dc.publisher Oxford University Press -
dc.title RAMP: response-aware multi-task learning with contrastive regularization for cancer drug response prediction -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Biochemical Research Methods;Mathematical & Computational Biology -
dc.relation.journalResearchArea Biochemistry & Molecular Biology;Mathematical & Computational Biology -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor multiomics -
dc.subject.keywordAuthor network embedding -
dc.subject.keywordAuthor multitask learning -
dc.subject.keywordAuthor contrastive learning -
dc.subject.keywordAuthor Bayesian neural network -
dc.subject.keywordPlus RESISTANCE -
dc.subject.keywordPlus SENSITIVITY -
dc.subject.keywordPlus LANDSCAPE -
dc.subject.keywordPlus LABEL -

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