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Nucleic Acids Res. 2012 Jun;40(11):e80. doi: 10.1093/nar/gks146. Epub 2012 Feb 22.

A fast ab-initio method for predicting miRNA precursors in genomes.

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1
Laboratoire IBISC, Université d'Evry-Val d'Essonne/Genopole, 23 Boulevard de France, 91034 Evry, France.

Abstract

miRNAs are small non coding RNA structures which play important roles in biological processes. Finding miRNA precursors in genomes is therefore an important task, where computational methods are required. The goal of these methods is to select potential pre-miRNAs which could be validated by experimental methods. With the new generation of sequencing techniques, it is important to have fast algorithms that are able to treat whole genomes in acceptable times. We developed an algorithm based on an original method where an approximation of miRNA hairpins are first searched, before reconstituting the pre-miRNA structure. The approximation step allows a substantial decrease in the number of possibilities and thus the time required for searching. Our method was tested on different genomic sequences, and was compared with CID-miRNA, miRPara and VMir. It gives in almost all cases better sensitivity and selectivity. It is faster than CID-miRNA, miRPara and VMir: it takes ≈ 30 s to process a 1 MB sequence, when VMir takes 30 min, miRPara takes 20 h and CID-miRNA takes 55 h. We present here a fast ab-initio algorithm for searching for pre-miRNA precursors in genomes, called miRNAFold. miRNAFold is available at http://EvryRNA.ibisc.univ-evry.fr/.

PMID:
22362754
PMCID:
PMC3367186
DOI:
10.1093/nar/gks146
[Indexed for MEDLINE]
Free PMC Article
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