Design space exploration of dataflow-based Smith-Waterman FPGA implementations

S. Brunet, E. Bezati, M. Mattavelli
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引用次数: 8

Abstract

The paper presents the results of design space explorations for the implementation of the Smith-Waterman (S-W) algorithm performing DNA and protein sequences alignment. Both design explorations studies and FPGA implementations are obtained by developing a dynamic dataflow program implementing the algorithm and by direct high-level synthesis (HLS) to FPGA HDL. The main feature of the obtained implementation is a low-latency, pipelinable multistage processing element (PE), providing a substantial decrease in resource utilization and increase in computation throughput when compared to state of the art solutions. The implementation solution is also fully scalable and can be efficiently reconfigured according to the DNA sequence sizes and performance requirements of the system architecture. The implementation solution presented in the paper can efficiently scale up to 250MHz obtaining 14746 Alignments/s using a single S-W core with 4 PEs, and up to 31.8 Mega-Alignments/min using 36 S-W cores on the same FPGA for sequences of 160×100 nucleotides.
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基于数据流的Smith-Waterman FPGA实现的设计空间探索
本文介绍了执行DNA和蛋白质序列比对的史密斯-沃特曼(S-W)算法实现的设计空间探索的结果。通过开发实现该算法的动态数据流程序,并直接对FPGA HDL进行高级合成(HLS),获得了设计探索研究和FPGA实现。所获得的实现的主要特点是低延迟、可管道化的多阶段处理元素(PE),与最先进的解决方案相比,大大降低了资源利用率,提高了计算吞吐量。实现方案也是完全可扩展的,可以根据DNA序列大小和系统架构的性能要求有效地重新配置。本文提出的实现方案可以有效地扩展到250MHz,使用单个带有4个pe的s - w内核获得14746个Alignments/s,在同一FPGA上使用36个s - w内核获得高达31.8个Mega-Alignments/min,用于160×100核苷酸序列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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