完整後設資料紀錄
DC 欄位語言
dc.contributor.authorHu, YJen_US
dc.date.accessioned2014-12-08T15:25:13Z-
dc.date.available2014-12-08T15:25:13Z-
dc.date.issued2005en_US
dc.identifier.isbn1-932415-83-1en_US
dc.identifier.urihttp://hdl.handle.net/11536/17605-
dc.description.abstractRNA plays a crucial role in post-transcriptional regulation. Similar to transcriptional regulation, post-transcriptional regulation is often accomplished by the binding of proteins to specific motifs in mRNA molecules. Unlike DNA binding proteins, which recognize motifs composed of conserved sequences, RNA protein binding sites are more conserved in structures than in sequences. A lot of works have been done for RNA structure prediction; however, most of them focus on single RNA structure prediction instead of finding characteristic structure motifs within a RNA family. Though some current approaches can now identify common structure motifs from a set of RNAs, they typically assume the given set forms a single family, which is not necessarily correct. We propose a new adaptive method that conducts structure prediction and clustering simultaneously. Its performance is demonstrated on several real RNA families.en_US
dc.language.isoen_USen_US
dc.subjectRNAen_US
dc.subjectsecondary structure elementen_US
dc.subjectclusteringen_US
dc.titleRNA clustering and secondary structure predictionen_US
dc.typeProceedings Paperen_US
dc.identifier.journalMETMBS '05: PROCEEDINGS OF THE 2005 INTERNATIONAL CONFERENCE ON MATHEMATICS AND ENGINEERING TECHNIQUES IN MEDICINE AND BIOLOGICAL SCIENCESen_US
dc.citation.spage59en_US
dc.citation.epage65en_US
dc.contributor.department資訊工程學系zh_TW
dc.contributor.departmentDepartment of Computer Scienceen_US
dc.identifier.wosnumberWOS:000236731800009-
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