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FPGA-based accelerator for adaptive banded event alignment in nanopore sequencing data analysis
Yilin Feng1, Zheyu Li2, Gulsum Gudukbay Akbulut2
1Department of Computer Science and Engineering, The Pennsylvania State University, 201 Old Main, University Park, PA, 16802, USA. ypf5071@psu.edu.
BMC Bioinformatics
|March 18, 2025
Summary
This study introduces an FPGA-based accelerator for Adaptive Banded Event Alignment (ABEA), enhancing DNA sequencing analysis. The new system offers significant speedups and energy savings over CPU and GPU implementations.
Area of Science:
- Genomics
- Bioinformatics
- Computer Engineering
Background:
- Adaptive Banded Event Alignment (ABEA) is crucial for Nanopore sequencing analysis, including sequence polishing and DNA methylation detection.
- Current ABEA implementations often rely on CPUs and GPUs.
- Field-Programmable Gate Arrays (FPGAs) offer potential for improved performance, cost-effectiveness, and energy efficiency in computational tasks.
Purpose of the Study:
- To develop and evaluate an efficient FPGA-based accelerator for the ABEA algorithm.
- To demonstrate the performance and energy benefits of using FPGAs for intensive genome analysis tasks.
Main Methods:
- Designed an FPGA-based accelerator leveraging the parallelism and sequential access patterns of the ABEA algorithm.
- Implemented the accelerator targeting a Xilinx VU9P FPGA.
- Compared the performance and energy consumption against CPU-based (Nanopolish) and GPU-based implementations.
Main Results:
- The FPGA-based ABEA accelerator achieved an average throughput speedup of 10.05x over CPU-only.
- It demonstrated a 1.81x speedup over state-of-the-art GPU acceleration while consuming only 7.2% of the energy.
- Achieved a 10.11x speedup compared to a previous FPGA accelerator.
Conclusions:
- Cutting-edge FPGAs can significantly benefit intensive genome analysis.
- FPGA acceleration offers substantial improvements in both performance and energy efficiency for bioinformatics algorithms like ABEA.

