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A Rapid High-throughput Method for Mapping Ribonucleoproteins (RNPs) on Human pre-mRNA
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BlastR--fast and accurate database searches for non-coding RNAs.

Giovanni Bussotti1, Emanuele Raineri, Ionas Erb

  • 1Bioinformatics and Genomics program, Center for Genomic Regulation (CRG) and UPF, Barcelona, C/ D. Aiguader, 88, 08003 Barcelona, Spain.

Nucleic Acids Research
|June 1, 2011
PubMed
Summary

BlastR is a new method for searching non-coding RNAs (ncRNAs) by comparing di-nucleotides with the BlosumR substitution matrix. This approach enhances sensitivity and speed compared to existing methods like BlastN and BlastP.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Accurate searching of non-coding RNA sequences is crucial for understanding gene regulation and function.
  • Existing sequence alignment tools like BlastN and BlastP have limitations in sensitivity and speed for non-coding RNA analysis.

Purpose of the Study:

  • To introduce and validate BlastR, a novel method for efficient and accurate non-coding RNA sequence searching.
  • To compare the performance of BlastR against established bioinformatics tools.

Main Methods:

  • Developed BlastR, a method utilizing di-nucleotide comparison with a new log-odd substitution matrix, BlosumR.
  • Recoded RNA sequences into protein-like sequences for compatibility with protein alignment algorithms.
  • Benchmarked BlastR against BlastN and BlastP using Rfam as a gold standard.

Main Results:

  • BlastR demonstrated higher sensitivity than BlastN for non-coding RNA searches.
  • BlastR proved to be faster and more sensitive than BlastP when using a single nucleotide substitution matrix.
  • When combined with WU-BlastP, BlastR showed a 5% increase in accuracy over WU-BlastN, albeit with a 50-fold increase in speed.

Conclusions:

  • BlastR offers a significant improvement in sensitivity and efficiency for non-coding RNA sequence searching.
  • The BlosumR substitution matrix and the recoding strategy are effective for aligning RNA sequences.
  • BlastR is a valuable open-source tool for the bioinformatics community, compatible with both WU-BlastP and NCBI-Blast packages.