Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/1169
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dc.contributor.authorTan, Mehmet-
dc.date.accessioned2019-06-26T07:40:35Z-
dc.date.available2019-06-26T07:40:35Z-
dc.date.issued2016-10-
dc.identifier.citationTan, M. (2016). Prediction of anti-cancer drug response by kernelized multi-task learning. Artificial intelligence in medicine, 73, 70-77.en_US
dc.identifier.issn0933-3657-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0933365716301920?via%3Dihub-
dc.identifier.urihttps://hdl.handle.net/20.500.11851/1169-
dc.description.abstractMotivation: Chemotherapy or targeted therapy are two of the main treatment options for many types of cancer. Due to the heterogeneous nature of cancer, the success of the therapeutic agents differs among patients. In this sense, determination of chemotherapeutic response of the malign cells is essential for establishing a personalized treatment protocol and designing new drugs. With the recent technological advances in producing large amounts of pharmacogenomic data, in silico methods have become important tools to achieve this aim. Objective: Data produced by using cancer cell lines provide a test bed for machine learning algorithms that try to predict the response of cancer cells to different agents. The potential use of these algorithms in drug discovery/repositioning and personalized treatments motivated us in this study to work on predicting drug response by exploiting the recent pharmacogenomic databases. We aim to improve the prediction of drug response of cancer cell lines. Methods: We propose to use a method that employs multi-task learning to improve learning by transfer, and kernels to extract non-linear relationships to predict drug response. Results: The method outperforms three state-of-the-art algorithms on three anti-cancer drug screen datasets. We achieved a mean squared error of 3.305 and 0.501 on two different large scale screen data sets. On a recent challenge dataset, we obtained an error of 0.556. We report the methodological comparison results as well as the performance of the proposed algorithm on each single drug. Conclusion: The results show that the proposed method is a strong candidate to predict drug response of cancer cell lines in silico for pre-clinical studies. The source code of the algorithm and data used can be obtained from http://mtan.etu.edu.tr/Supplementary/kMTrace/. (C) 2016 Elsevier B.V. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofArtificial intelligence in Medicineen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMulti-Task Learningen_US
dc.subjectDrug Response Predictionen_US
dc.subjectCancer Cell Linesen_US
dc.subjectGene Expression Dataen_US
dc.titlePrediction of Anti-Cancer Drug Response by Kernelized Multi-Task Learningen_US
dc.typeArticleen_US
dc.departmentFaculties, Faculty of Engineering, Department of Computer Engineeringen_US
dc.departmentFakülteler, Mühendislik Fakültesi, Bilgisayar Mühendisliği Bölümütr_TR
dc.identifier.volume73-
dc.identifier.startpage70-
dc.identifier.endpage77-
dc.relation.tubitakScientific and Technological Research Council of Turkey, Career Grant Program [115E274]en_US
dc.authorid0000-0002-1741-0570-
dc.identifier.wosWOS:000388046500006en_US
dc.identifier.scopus2-s2.0-84992126922en_US
dc.institutionauthorTan, Mehmet-
dc.identifier.pmid27926382en_US
dc.identifier.doi10.1016/j.artmed.2016.09.004-
dc.authorwosidI-2328-2019-
dc.authorscopusid36984623900-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopusqualityQ2-
item.openairetypeArticle-
item.languageiso639-1en-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.dept02.1. Department of Artificial Intelligence Engineering-
Appears in Collections:Bilgisayar Mühendisliği Bölümü / Department of Computer Engineering
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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