Abstract
Genome sequences contain hundreds of millions of DNA base pairs. Finding the degree of similarity between two genomes requires executing a compute-intensive dynamic programming algorithm, such as Smith-Waterman. Traditional von Neumann architectures have limited parallelism and cannot provide an efficient solution for large-scale genomic data. Approximate heuristic methods (e.g. BLAST) are commonly used. However, they are suboptimal and still compute-intensive. In this work, we present BioSEAL, a biological sequence alignment accelerator. BioSEAL is a massively parallel non-von Neumann processing-in-memory architecture for large-scale DNA and protein sequence alignment. BioSEAL is based on resistive content addressable memory, capable of energy-efficient and highperformance associative processing. We present an associative processing algorithm for entire database sequence alignment on BioSEAL and compare its performance and power consumption with state-of-art solutions. We show that BioSEAL can achieve up to 57× speedup and 156× better energy efficiency, compared with existing solutions for genome sequence alignment and protein sequence database search.
Cite
CITATION STYLE
Kaplan, R., Yavits, L., & Ginosasr, R. (2020). BioSEAL: In-Memory Biological Sequence Alignment Accelerator for Large-Scale Genomic Data. In SYSTOR 2020 - Proceedings of the 13th ACM International Systems and Storage Conference (pp. 36–48). Association for Computing Machinery. https://doi.org/10.1145/3383669.3398279
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