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dc.contributor.authorJeggari, Ashwini
dc.contributor.authorMarks, Debora
dc.contributor.authorLarsson, Erik
dc.date.accessioned2013-03-19T16:23:42Z
dc.date.issued2012
dc.identifier.citationJeggari, Ashwini, Debora S Marks, and Erik Larsson. 2012. miRcode: A map of putative microrna target sites in the long non-coding transcriptome. Bioinformatics 28(15): 2062-2063.en_US
dc.identifier.issn1367-4803en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:10445586
dc.description.abstractSummary: Although small non-coding RNAs, such as microRNAs, have well-established functions in the cell, long non-coding RNAs (lncRNAs) have only recently started to emerge as abundant regulators of cell physiology, and their functions may be diverse. A small number of studies describe interactions between small and lncRNAs, with lncRNAs acting either as inhibitory decoys or as regulatory targets of microRNAs, but such interactions are still poorly explored. To facilitate the study of microRNA–lncRNA interactions, we implemented miRcode: a comprehensive searchable map of putative microRNA target sites across the complete GENCODE annotated transcriptome, including 10 419 lncRNA genes in the current version.en_US
dc.language.isoen_USen_US
dc.publisherOxford University Pressen_US
dc.relation.isversionofdoi:10.1093/bioinformatics/bts344en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400968/pdf/en_US
dash.licenseLAA
dc.subjectSequence Analysisen_US
dc.titlemiRcode: A map of putative microRNA target sites in the long non-coding transcriptomeen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalBioinformaticsen_US
dash.depositing.authorMarks, Debora
dc.date.available2013-03-19T16:23:42Z
dc.identifier.doi10.1093/bioinformatics/bts344*
dash.contributor.affiliatedMarks, Debora


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