Low power reprogrammable DNA basecaller with an efficient HMM accelerator for real time nanopore sequencing
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Published on: June 3, 2019
Atefeh Salimi Shahraki1, Sebastian Magierowski2, Mahdi Abbasi3,4,5
1Department of Electrical Engineering, Isf.C, Islamic Azad University, Isfahan, Iran. atefehsalimi@iau.ac.ir.
Abstract:
Basecalling is a crucial step in DNA sequencing that converts raw nanopore signals into nucleotide sequences. This paper presents a serial-parallel reprogrammable DNA sequencing accelerator based on a 64-state Hidden Markov Model (HMM) implemented in a 130-nm CMOS process. The proposed method optimizes computational efficiency, hardware utilization, and power consumption using a coarse-grained serial-parallel processing approach. It achieves 94.3% accuracy, outperforming Nanocall (85.6%) and Meta-Align (91.2%), while being slightly superior to the Scalable Hardware Accelerator (93.1%). Furthermore, it consumes 200 mW, which is 6 times lower than brute-force HMM implementations and 3–5 times more power-efficient than deep learning-based basecallers like DeepNano and Bonito. The proposed accelerator maintains competitive throughput at 8 M Bases/sec, balancing processing speed and energy efficiency. Additionally, the architecture supports scalability up to 4096 states, making it highly adaptable for various sequencing applications. It’s hardware-optimized and low-power design makes it an ideal alternative to brute-force and software-based methods for real-time, mobile, and embedded DNA sequencing devices.

