article Open AccessTop 1% cited
Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites
Genome biology · 2010 · Vol. 11(8) · pp. R90–R90
Doron Betel✉(Memorial Sloan Kettering Cancer Center)Anjali Koppal(Columbia University)Phaedra Agius(Memorial Sloan Kettering Cancer Center)Chris Sander(Memorial Sloan Kettering Cancer Center)Christina S. Leslie(Memorial Sloan Kettering Cancer Center)
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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Nature Genetics · 2007 · 2,505 citations
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