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Published on: August 18, 2018
Fast filtering for RNA homology search
1Janelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
Bioinformatics (Oxford, England)
|October 4, 2011
Summary
This study introduces a faster RNA homology search method using ungapped structural alignment. The multi-segment CYK filter significantly reduces computation time and space requirements for identifying RNA sequences.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- RNA homology search benefits from secondary structure information, but traditional methods like covariance models are computationally expensive.
- Existing acceleration strategies often use sequence-only filters, potentially losing structural information.
Purpose of the Study:
- To develop a computationally efficient filter for RNA homology search that incorporates secondary structure information.
- To improve the speed and scalability of RNA secondary structure-based homology detection.
Main Methods:
- Introduction of the multi-segment CYK (MSCYK) filter, employing a heuristic of ungapped structural alignment.
- Implementation of a vector-parallel approach for the MSCYK filter.
- Integration of MSCYK with existing gapped alignment methods into a filtering pipeline.
Main Results:
- The MSCYK filter reduces computational time complexity from O(N⁴) to O(N³) and space complexity from O(N³) to O(N²).
- Vector-parallel implementation of MSCYK achieves up to a 100-fold speed-up compared to standard methods.
- Combined filtering pipeline shows synergistic results, maintaining RNA secondary structure scoring throughout.
Conclusions:
- The MSCYK filter provides a significant computational advantage for RNA homology searches.
- This method enhances the efficiency of RNA secondary structure analysis in large-scale genomic studies.
- The developed filtering pipeline offers a powerful and scalable approach for RNA bioinformatics.
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