Development of computational models using omics data for the identification of effective cancer metabolic biomarkers

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dc.contributor.authorLee, Sang Miko
dc.contributor.authorKim, Hyun Ukko
dc.date.accessioned2021-12-15T06:40:36Z-
dc.date.available2021-12-15T06:40:36Z-
dc.date.created2021-10-18-
dc.date.created2021-10-18-
dc.date.issued2021-12-
dc.identifier.citationMOLECULAR OMICS, v.17, no.6, pp.881 - 893-
dc.identifier.issn2515-4184-
dc.identifier.urihttp://hdl.handle.net/10203/290667-
dc.description.abstractIdentification of novel biomarkers has been an active area of study for the effective diagnosis, prognosis and treatment of cancers. Among various types of cancer biomarkers, metabolic biomarkers, including enzymes, metabolites and metabolic genes, deserve attention as they can serve as a reliable source for diagnosis, prognosis and treatment of cancers. In particular, efforts to identify novel biomarkers have been greatly facilitated by a rapid increase in the volume of multiple omics data generated for a range of cancer cells. These omics data in turn serve as ingredients for developing computational models that can help derive deeper insights into the biology of cancer cells, and identify metabolic biomarkers. In this review, we provide an overview of omics data generated for cancer cells, and discuss recent studies on computational models that were developed using omics data in order to identify effective cancer metabolic biomarkers.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleDevelopment of computational models using omics data for the identification of effective cancer metabolic biomarkers-
dc.typeArticle-
dc.identifier.wosid000703629600001-
dc.type.rimsART-
dc.citation.volume17-
dc.citation.issue6-
dc.citation.beginningpage881-
dc.citation.endingpage893-
dc.citation.publicationnameMOLECULAR OMICS-
dc.identifier.doi10.1039/d1mo00337b-
dc.contributor.localauthorKim, Hyun Uk-
dc.contributor.nonIdAuthorLee, Sang Mi-
dc.description.isOpenAccessN-
dc.type.journalArticleReview-
dc.subject.keywordPlusPARTIAL LEAST-SQUARES-
dc.subject.keywordPlusREGRESSION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusNETWORK-
dc.subject.keywordPlusHMDB-
dc.subject.keywordPlusFLUX-
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