Hairpins in a Haystack: recognizing microRNA precursors in comparative genomics data.
basic_science · Level V
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Abstract
Recently, genome-wide surveys for non-coding RNAs have provided evidence for tens of thousands of previously undescribed evolutionary conserved RNAs with distinctive secondary structures. The annotation of these putative ncRNAs, however, remains a difficult problem. Here we describe an SVM-based approach that, in conjunction with a non-stringent filter for consensus secondary structures, is capable of efficiently recognizing microRNA precursors in multiple sequence alignments. The software was applied to recent genome-wide RNAz surveys of mammals, urochordates, and nematodes. The program RNAmicro is available as source code and can be downloaded from http://www.bioinf.uni-leipzig/Software/RNAmicro.
Medical subject headings
- Chromosome Mapping
- Databases, Genetic
- MicroRNAs
- RNA Precursors
- Sequence Alignment
- Sequence Analysis, RNA