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Random Forest in Splice Site Prediction of Human Genome

dc.contributor.authorPashaei, Elham
dc.contributor.authorOzen, Mustafa
dc.contributor.authorAydin, Nizamettin
dc.date.accessioned2026-06-27T13:47:24Z
dc.date.issued2016
dc.description.abstractWith the rapid growth of huge amounts of DNA sequence, genes identification has become an important task in bioinformatics. To detect genes, it is important to accurately predict splice sites, i.e. exon intron boundaries. Moreover, in biology where structures are described by a large number of features as splice sites, the feature selection is an important step toward the classification task. It provides useful biological knowledge and allows for a faster and better classification. Feature selection techniques can be divided into two groups: feature-ranking and feature-subset selection. This paper investigates the performance of combining support vector machine (SVM) with two different feature ranking methods, namely F-score and Random Forest feature ranking competitively in splice site detection of Human genome. Also a new classification method based on Random Forest for splice site prediction is presented.en
dc.description.urihttps://doi.org/10.1007/978-3-319-32703-7_99
dc.identifier.doi10.1007/978-3-319-32703-7_99
dc.identifier.endpage517
dc.identifier.isbn978-3-319-32703-7; 978-3-319-32701-3
dc.identifier.issn1680-0737
dc.identifier.startpage512
dc.identifier.urihttps://hdl.handle.net/20.500.14981/54840
dc.identifier.volume57
dc.identifier.wos000376283000099
dc.language.isoeng
dc.publisherSPRINGER
dc.relation.conference14th Mediterranean Conference on Medical and Biological Engineering and Computing (MEDICON)
dc.relation.ispartofXIV MEDITERRANEAN CONFERENCE ON MEDICAL AND BIOLOGICAL ENGINEERING AND COMPUTING 2016
dc.subjectRandom Forest
dc.subjectFeature ranking
dc.subjectSplice site prediction
dc.subjectEngineering
dc.subjectMaterials Science
dc.titleRandom Forest in Splice Site Prediction of Human Genome
dc.typeProceedings Paper
dspace.entity.typePublication
local.import.sourceWOS

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