MASTR: multiple alignment and structure prediction of non-coding RNAs using simulated annealing

Motivation: As more non–coding RNAs are discovered, the importance of methods for RNA analysis increases. Since the structure of ncRNA is intimately tied to the function of the molecule, programs for RNA structure prediction are necessary tools in this growing field of research. Furthermore, it is k...

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Published inBioinformatics Vol. 23; no. 24; pp. 3304 - 3311
Main Authors Lindgreen, Stinus, Gardner, Paul P., Krogh, Anders
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 15.12.2007
Oxford Publishing Limited (England)
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ISSN1367-4803
1367-4811
1460-2059
1367-4811
DOI10.1093/bioinformatics/btm525

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Summary:Motivation: As more non–coding RNAs are discovered, the importance of methods for RNA analysis increases. Since the structure of ncRNA is intimately tied to the function of the molecule, programs for RNA structure prediction are necessary tools in this growing field of research. Furthermore, it is known that RNA structure is often evolutionarily more conserved than sequence. However, few existing methods are capable of simultaneously considering multiple sequence alignment and structure prediction. Result: We present a novel solution to the problem of simultaneous structure prediction and multiple alignment of RNA sequences. Using Markov chain Monte Carlo in a simulated annealing framework, the algorithm MASTR (Multiple Alignment of STructural RNAs) iteratively improves both sequence alignment and structure prediction for a set of RNA sequences. This is done by minimizing a combined cost function that considers sequence conservation, covariation and basepairing probabilities. The results show that the method is very competitive to similar programs available today, both in terms of accuracy and computational efficiency. Availability: Source code available from http://mastr.binf.ku.dk/ Contact: stinus@binf.ku.dk
Bibliography:Associate Editor: Dmitrij Frishman
To whom correspondence should be addressed.
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ISSN:1367-4803
1367-4811
1460-2059
1367-4811
DOI:10.1093/bioinformatics/btm525