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Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites

Genome biology · 2010 · Vol. 11(8) · pp. R90–R90
Doron BetelAnjali KoppalPhaedra AgiusChris SanderChristina S. Leslie

Abstract

mirSVR is a new machine learning method for ranking microRNA target sites by a down-regulation score. The algorithm trains a regression model on sequence and contextual features extracted from miRanda-predicted target sites. In a large-scale evaluation, miRanda-mirSVR is competitive with other target prediction methods in identifying target genes and predicting the extent of their downregulation at the mRNA or protein levels. Importantly, the method identifies a significant number of experimentally determined non-canonical and non-conserved sites.

MicroRNA in disease regulationRNA Interference and Gene DeliveryCircular RNAs in diseasesBiologyComputational biologyHuman geneticsmicroRNAGenome BiologyEvolutionary biologyGeneticsConserved sequenceGenomeGenomics

MeSH terms

AlgorithmsArtificial IntelligenceBinding SitesModels, MolecularProteinsRegression AnalysisRNA, MessengerDown-RegulationMicroRNAs

Funding

  • National Institutes of Health
Citations
1,625
FWCI
26.27
field-weighted impact
References
39
Percentile
100%
vs. same field & year
Citations per year
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References
Most mammalian mRNAs are conserved targets of microRNAs
Genome Research · 2008 · 8,505 citations
Human MicroRNA Targets
PLoS Biology · 2004 · 3,885 citations
Combinatorial microRNA target predictions
Nature Genetics · 2005 · 4,610 citations
MicroRNA targets in Drosophila
Genome biology · 2003 · 3,718 citations
The role of site accessibility in microRNA target recognition
Nature Genetics · 2007 · 2,505 citations
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