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dc.contributor.advisorHalaas, Arnenb_NO
dc.contributor.advisorSætrom, Pålnb_NO
dc.contributor.authorSætrom, Olanb_NO
dc.date.accessioned2014-12-19T13:33:15Z
dc.date.available2014-12-19T13:33:15Z
dc.date.created2010-09-03nb_NO
dc.date.issued2005nb_NO
dc.identifier348133nb_NO
dc.identifierntnudaim:1087nb_NO
dc.identifier.urihttp://hdl.handle.net/11250/251026
dc.description.abstractMicroRNAs are a large family of short non-encoding RNAs that regulated protein production by binding to mRNAs. A single miRNA can regulate an mRNA by itself, or several miRNAs can cooperate in regulating the mRNAs. This is all dependent on the degree of complementarity between the miRNA and the target mRNA. Here, we present the program TargetBoost that, using a classifier generated by a combination of hardware accelerated genetic programming and boosting, allows for screening several large dataset against several miRNAs, and computes a likelihood of that genes in the dataset is regulated by the set of miRNAs used in the screening. We also present results from comparison of several different scoring functions for measuring cooperative effects. We found that the classifier used in TargetBoost is best for finding target sites that regulate mRNAs by themselves. A demo of TargetBoost can be found on http://www.interagon.com/demo.nb_NO
dc.languageengnb_NO
dc.publisherInstitutt for datateknikk og informasjonsvitenskapnb_NO
dc.subjectntnudaimno_NO
dc.subjectSIF2 datateknikkno_NO
dc.subjectProgram- og informasjonssystemerno_NO
dc.titlePredicting MicroRNA targetsnb_NO
dc.typeMaster thesisnb_NO
dc.source.pagenumber82nb_NO
dc.contributor.departmentNorges teknisk-naturvitenskapelige universitet, Fakultet for informasjonsteknologi, matematikk og elektroteknikk, Institutt for datateknikk og informasjonsvitenskapnb_NO


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