Abstract

BackgroundIn recent years, the important functional roles of RNAs in biological processes have been repeatedly demonstrated. Computing the similarity between two RNAs contributes to better understanding the functional relationship between them. But due to the long-range correlations of RNA, many efficient methods of detecting protein similarity do not work well. In order to comprehensively understand the RNA’s function, the better similarity measure among RNAs should be designed to consider their structure features (base pairs). Current methods for RNA comparison could be generally classified into alignment-based and alignment-free.ResultsIn this paper, we propose a novel wavelet-based method based on RNA triple vector curve representation, named multi-scale RNA comparison. Firstly, we designed a novel numerical representation of RNA secondary structure termed as RNA triple vectors curve (TV-Curve). Secondly, we constructed a new similarity metric based on the wavelet decomposition of the TV-Curve of RNA. Finally we also applied our algorithm to the classification of non-coding RNA and RNA mutation analysis. Furthermore, we compared the results to the two well-known RNA comparison tools: RNAdistance and RNApdist. The results in this paper show the potentials of our method in RNA classification and RNA mutation analysis.ConclusionWe provide a better visualization and analysis tool named TV-Curve of RNA, especially for long RNA, which can characterize both sequence and structure features. Additionally, based on TV-Curve representation of RNAs, a multi-scale similarity measure for RNA comparison is proposed, which can capture the local and global difference between the information of sequence and structure of RNAs. Compared with the well-known RNA comparison approaches, the proposed method is validated to be outstanding and effective in terms of non-coding RNA classification and RNA mutation analysis. From the numerical experiments, our proposed method can capture more efficient and subtle relationship of RNAs.

Highlights

  • In recent years, the important functional roles of RNAs in biological processes have been repeatedly demonstrated

  • Numerous approaches were proposed to measure the similarity between RNA secondary structures, which can be broadly categorized into two classes: alignment based string or tree representation of RNA secondary structure, and comparison based some numerical representation without alignment

  • Similarities/dissimilarities among the RNA secondary structures of nine virus To further illustrate the utility of our approach for the subtle structure comparison, we examine similarities / dissimilarities of a set of relatively similar RNA secondary structures at the 3’-terminus of nine different viruses

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Summary

Introduction

The important functional roles of RNAs in biological processes have been repeatedly demonstrated. Computing the similarity between two RNAs contributes to better understanding the functional relationship between them. In order to comprehensively understand the RNA’s function, the better similarity measure among RNAs should be designed to consider their structure features (base pairs). Numerous approaches were proposed to measure the similarity between RNA secondary structures, which can be broadly categorized into two classes: alignment based string or tree representation of RNA secondary structure, and comparison based some numerical representation without alignment. Some are usually based on the alignment of a string representation of the secondary structures such as the dot-bracket representation, in which a score function or a distance function to represent insertion, deletion and substitution of letters in the compared structures [1,2,3,4]. Sequences considered in alignment of RNA secondary structures are string sequences and secondary structure. Different weights or different score functions are designed for unpaired nucleotides and paired nucleotides

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