Zhenjiang Xu1, David H Mathews. 1. Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, NY, USA.
Abstract
MOTIVATION: With recent advances in sequencing, structural and functional studies of RNA lag behind the discovery of sequences. Computational analysis of RNA is increasingly important to reveal structure-function relationships with low cost and speed. The purpose of this study is to use multiple homologous sequences to infer a conserved RNA structure. RESULTS: A new algorithm, called Multilign, is presented to find the lowest free energy RNA secondary structure common to multiple sequences. Multilign is based on Dynalign, which is a program that simultaneously aligns and folds two sequences to find the lowest free energy conserved structure. For Multilign, Dynalign is used to progressively construct a conserved structure from multiple pairwise calculations, with one sequence used in all pairwise calculations. A base pair is predicted only if it is contained in the set of low free energy structures predicted by all Dynalign calculations. In this way, Multilign improves prediction accuracy by keeping the genuine base pairs and excluding competing false base pairs. Multilign has computational complexity that scales linearly in the number of sequences. Multilign was tested on extensive datasets of sequences with known structure and its prediction accuracy is among the best of available algorithms. Multilign can run on long sequences (> 1500 nt) and an arbitrarily large number of sequences. AVAILABILITY: The algorithm is implemented in ANSI C++ and can be downloaded as part of the RNAstructure package at: http://rna.urmc.rochester.edu.
MOTIVATION: With recent advances in sequencing, structural and functional studies of RNA lag behind the discovery of sequences. Computational analysis of RNA is increasingly important to reveal structure-function relationships with low cost and speed. The purpose of this study is to use multiple homologous sequences to infer a conserved RNA structure. RESULTS: A new algorithm, called Multilign, is presented to find the lowest free energy RNA secondary structure common to multiple sequences. Multilign is based on Dynalign, which is a program that simultaneously aligns and folds two sequences to find the lowest free energy conserved structure. For Multilign, Dynalign is used to progressively construct a conserved structure from multiple pairwise calculations, with one sequence used in all pairwise calculations. A base pair is predicted only if it is contained in the set of low free energy structures predicted by all Dynalign calculations. In this way, Multilign improves prediction accuracy by keeping the genuine base pairs and excluding competing false base pairs. Multilign has computational complexity that scales linearly in the number of sequences. Multilign was tested on extensive datasets of sequences with known structure and its prediction accuracy is among the best of available algorithms. Multilign can run on long sequences (> 1500 nt) and an arbitrarily large number of sequences. AVAILABILITY: The algorithm is implemented in ANSI C++ and can be downloaded as part of the RNAstructure package at: http://rna.urmc.rochester.edu.
Authors: Hakim Tafer; Stefan L Ameres; Gregor Obernosterer; Christoph A Gebeshuber; Renée Schroeder; Javier Martinez; Ivo L Hofacker Journal: Nat Biotechnol Date: 2008-04-27 Impact factor: 54.908
Authors: Franck A P Vendeix; Agnieszka Dziergowska; Estella M Gustilo; William D Graham; Brian Sproat; Andrzej Malkiewicz; Paul F Agris Journal: Biochemistry Date: 2008-05-13 Impact factor: 3.162
Authors: Cynthia M Sharma; Steve Hoffmann; Fabien Darfeuille; Jérémy Reignier; Sven Findeiss; Alexandra Sittka; Sandrine Chabas; Kristin Reiche; Jörg Hackermüller; Richard Reinhardt; Peter F Stadler; Jörg Vogel Journal: Nature Date: 2010-02-17 Impact factor: 49.962
Authors: Stephan H Bernhart; Ivo L Hofacker; Sebastian Will; Andreas R Gruber; Peter F Stadler Journal: BMC Bioinformatics Date: 2008-11-11 Impact factor: 3.169