Abstract

The prediction of RNA secondary structure can be facilitated by incorporating with comparative analysis of homologous sequences. However, most of existing comparative methods are vulnerable to alignment errors and thus are of low accuracy in practical application. Here we improve the prediction of RNA secondary structure by detecting and assessing conserved stems shared by all sequences in the alignment. Our method can be summarized by: 1) we detect possible stems in single RNA sequence using the so-called position matrix with which some possibly paired positions can be uncovered; 2) we detect conserved stems across multiple RNA sequences by multiplying the position matrices; 3) we assess the conserved stems using the Signal-to-Noise; 4) we compute the optimized secondary structure by incorporating the so-called reliable conserved stems with predictions by RNAalifold program. We tested our method on data sets of RNA alignments with known secondary structures. The accuracy, measured as sensitivity and specificity, of our method is greater than predictions by RNAalifold.

Highlights

  • In recent years, RNAs gained increasing interest since a huge variety of functions associated with them were found [1]

  • The prediction of RNA secondary structure can be facilitated by incorporating with comparative analysis of homologous sequences

  • Our method can be summarized by: 1) we detect possible stems in single RNA sequence using the so-called position matrix with which some possibly paired positions can be uncovered; 2) we detect conserved stems across multiple RNA sequences by multiplying the position matrices; 3) we assess the conserved stems using the Signal-to-Noise; 4) we compute the optimized secondary structure by incorporating the so-called reliable conserved stems with predictions by RNAalifold program

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Summary

Introduction

RNAs gained increasing interest since a huge variety of functions associated with them were found [1]. The current physical methods available for structure determination are time-consuming and expensive [4] For this reason, computational prediction provides an attractive alternative to facilitate the discovery of RNA secondary structure. A number of methods based on comparative analysis of homologous sequences have been implemented to predict RNA secondary structure [8,9,10,11,12]. These approaches depend on fixed alignments and are very vulnerable to alignment errors. Algorithms based on these methods are too computationally taxing to be practical

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