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dc.contributor.author박현석*
dc.date.accessioned2022-06-02T16:32:20Z-
dc.date.available2022-06-02T16:32:20Z-
dc.date.issued2022*
dc.identifier.issn2234-0742*
dc.identifier.otherOAK-31567*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/261364-
dc.description.abstractA major issue in the use of immune checkpoint inhibitors is their lack of efficacy in many patients. Previous studies have reported that the T cell inflamed signature can help predict the response to immunotherapy. Thus, many studies have investigated mechanisms of im-munotherapy resistance by defining the tumor microenvironment based on T cell inflamed and non–T cell inflamed subsets. Although methods of calculating T cell inflamed subsets have been developed, valid screening tools for distinguishing T cell inflamed from non–T cell inflamed subsets using gene expression data are still needed, since general researchers who are unfamiliar with the details of the equations can experience difficulties using ex-tant scoring formulas to conduct analyses. Thus, we introduce TcellInflamedDetector, an R package for distinguishing T cell inflamed from non–T cell inflamed samples using cancer gene expression data via bulk RNA sequencing. © 2022 Korea Genome Organization.*
dc.languageEnglish*
dc.publisherKorea Genome Organization*
dc.subjectgene expression*
dc.subjectimmune checkpoint inhibitors*
dc.subjectimmunotherapy*
dc.subjectprognosis*
dc.subjectRNA-seq*
dc.subjectsoftware*
dc.titleTcellInflamedDetector: an R package to distinguish T cell inflamed tumor types from non–T cell inflamed tumor types*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume20*
dc.relation.indexSCOPUS*
dc.relation.journaltitleGenomics and Informatics*
dc.identifier.doi10.5808/gi.22005*
dc.identifier.scopusid2-s2.0-85128856528*
dc.author.googleYang S.-D.*
dc.author.googlePark H.-S.*
dc.contributor.scopusid박현석(22433646000)*
dc.date.modifydate20240322133434*
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인공지능대학 > 컴퓨터공학과 > Journal papers
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