RAPIDx: A ReRAM Processing in-Memory Architecture for DNA Short Read Alignment
Published in American Society of Human Genetics (ASHG) 2020, 2020
Recommended citation: Gupta S, Imani M, Khaleghi B, Moshiri N, Rosing T (2020). "RAPIDx: A ReRAM Processing in-Memory Architecture for DNA Short Read Alignment." American Society of Human Genetics (ASHG) 2020. Poster.
Sequence alignment is a core component of many biological applications. As the advancement in sequencing technologies produces a tremendous amount of data on an hourly basis, this alignment is becoming the critical bottleneck in bioinformatics analysis. Even though large clusters and highly-parallel processing nodes can carry out sequence alignment, in addition to the exacerbated power consumption, they cannot afford to concurrently process the massive amount of data generated by sequencing machines. In this paper, we propose a novel processing in-memory (PIM) architecture suited for DNA sequence alignment, called RAPIDx. We revise the state-of-the-art alignment algorithm to make it compatible with in- memory parallel computations, and process DNA data completely inside memory without requiring additional processing units. The main advantage of RAPIDx over the other alignment accelerators is a dramatic reduction in internal data movement while maintaining a remarkable degree of parallelism provided by PIM. The proposed architecture is also highly scalable, facilitating precise alignment of lengthy sequences. We also implement different scoring schemes which enable high scoring alignments. In addition, we enable an optimized implementation which decreases the energy consumption of DNA alignment at the cost of negligible accuracy loss. We evaluated the efficiency of the proposed architecture by aligning chromosome sequences from human and chimpanzee genomes. The results show that RAPIDx is at least 2× faster and 7× more power efficient than BioSEAL, the best DNA sequence alignment accelerator.