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Open Access Methodology article

Multithreaded comparative RNA secondary structure prediction using stochastic context-free grammars

Zsuzsanna Sükösd12*, Bjarne Knudsen3, Morten Værum3, Jørgen Kjems12 and Ebbe S Andersen12*

Author Affiliations

1 Interdisciplinary Nanoscience Center, Aarhus University, Aarhus, Denmark

2 Department of Molecular Biology, Aarhus University, Aarhus, Denmark

3 CLC bio, Aarhus, Denmark

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BMC Bioinformatics 2011, 12:103  doi:10.1186/1471-2105-12-103

Published: 18 April 2011

Abstract

Background

The prediction of the structure of large RNAs remains a particular challenge in bioinformatics, due to the computational complexity and low levels of accuracy of state-of-the-art algorithms. The pfold model couples a stochastic context-free grammar to phylogenetic analysis for a high accuracy in predictions, but the time complexity of the algorithm and underflow errors have prevented its use for long alignments. Here we present PPfold, a multithreaded version of pfold, which is capable of predicting the structure of large RNA alignments accurately on practical timescales.

Results

We have distributed both the phylogenetic calculations and the inside-outside algorithm in PPfold, resulting in a significant reduction of runtime on multicore machines. We have addressed the floating-point underflow problems of pfold by implementing an extended-exponent datatype, enabling PPfold to be used for large-scale RNA structure predictions. We have also improved the user interface and portability: alongside standalone executable and Java source code of the program, PPfold is also available as a free plugin to the CLC Workbenches. We have evaluated the accuracy of PPfold using BRaliBase I tests, and demonstrated its practical use by predicting the secondary structure of an alignment of 24 complete HIV-1 genomes in 65 minutes on an 8-core machine and identifying several known structural elements in the prediction.

Conclusions

PPfold is the first parallelized comparative RNA structure prediction algorithm to date. Based on the pfold model, PPfold is capable of fast, high-quality predictions of large RNA secondary structures, such as the genomes of RNA viruses or long genomic transcripts. The techniques used in the parallelization of this algorithm may be of general applicability to other bioinformatics algorithms.