Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2105-7-S5-S20
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dc.titleMicroTar: Predicting microRNA targets from RNA duplexes
dc.contributor.authorThadani, R.
dc.contributor.authorTammi, M.T.
dc.date.accessioned2014-10-27T08:33:29Z
dc.date.available2014-10-27T08:33:29Z
dc.date.issued2006-12-18
dc.identifier.citationThadani, R., Tammi, M.T. (2006-12-18). MicroTar: Predicting microRNA targets from RNA duplexes. BMC Bioinformatics 7 (SUPPL.5) : -. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2105-7-S5-S20
dc.identifier.issn14712105
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/101096
dc.description.abstractBackground: The accurate prediction of a comprehensive set of messenger RNAs (targets) regulated by animal microRNAs (miRNAs) remains an open problem. In particular, the prediction of targets that do not possess evolutionarily conserved complementarity to their miRNA regulators is not adequately addressed by current tools. Results: We have developed MicroTar, an animal miRNA target prediction tool based on miRNA-target complementarity and thermodynamic data. The algorithm uses predicted free energies of unbound mRNA and putative mRNA-miRNA heterodimers, implicitly addressing the accessibility of the mRNA 3′ untranslated region. MicroTar does not rely on evolutionary conservation to discern functional targets, and is able to predict both conserved and non-conserved targets. MicroTar source code and predictions are accessible at http://tiger.dbs.nus.edu.sg/microtar/, where both serial and parallel versions of the program can be downloaded under an open-source licence. Conclusion: MicroTar achieves better sensitivity than previously reported predictions when tested on three distinct datasets of experimentally-verified miRNA-target interactions in C elegans, Drosophila, and mouse. © 2006 Thadani and Tammi; licensee BioMed Central Ltd.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1186/1471-2105-7-S5-S20
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1186/1471-2105-7-S5-S20
dc.description.sourcetitleBMC Bioinformatics
dc.description.volume7
dc.description.issueSUPPL.5
dc.description.page-
dc.description.codenBBMIC
dc.identifier.isiut000244789800020
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