Efficiency of Learned Indexes on Genome Spectra
Md Hasin Abrar1, Paul Medvedev1,2,3, Giorgio Vinciguerra4
1Department of Computer Science and Engineering, Penn State, University Park, PA, USA.
Summary
We introduce CaPLa, a new measure for data structure performance on genomic k-mers. CaPLa predicts efficiency by analyzing data patterns, improving bioinformatics tool design for large datasets.
Area of Science:
- Bioinformatics
- Computational Biology
- Data Structures
Background:
- Genomic data structures rely on patterns in k-mer multisets for efficiency.
- Learned indexes approximate data functions but lack predictive theoretical analysis.
- Practical performance of learned indexes is hard to predict from worst-case analysis.
Purpose of the Study:
- Develop a novel measure, CaPLa, for piecewise-linear approximability of genomic k-mer multisets.
- Enable accurate prediction of space bounds for bioinformatics data structures.
- Understand the variability of data patterns across genomes.
Main Methods:
- Introduced CaPLa (Canonical Piecewise Linear approximability) based on power-law models and deviations.
- Developed an efficient algorithm for CaPLa computation.
- Analyzed over 500 genomes using CaPLa to assess its predictive power and variability.
Main Results:
- CaPLa accurately predicts space bounds for data structures on real genomic data.
- Empirical analysis revealed wide variation in CaPLa across the tree of life and within genomes.
- Identified factors contributing to the non-random nature of genomic k-mer multisets.
Conclusions:
- CaPLa provides a robust measure for predicting the performance of learned indexes on genomic data.
- Understanding k-mer multiset approximability is crucial for efficient bioinformatics tool development.
- Genomic data exhibits unique patterns that CaPLa effectively quantifies.
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