生物信息学中序列比对问题的粗粒可重构结构

Pei Liu, A. Hemani
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引用次数: 4

摘要

提出了一种用于加速生物信息学算法的粗粒可重构结构(CGRA)。关键的创新是一个轻量级的生物信息学处理器,可以重新配置以执行不同的添加比较和选择操作的流行的测序算法。可编程和可扩展的体系结构平台实例化了这种处理元素的阵列,并允许任意分区和调度方案,能够解决包括顺序阶段在内的完整排序算法,并处理任意大的序列。与基于FPGA和GPU的解决方案相比,所提出的基于CGRA的解决方案的关键区别在于,它能够更好地匹配核心计算需求和系统级架构需求的体系结构和算法。这种说法可以用三种流行的测序算法来量化:Needleman-Wunsch、Smith-Waterman和HMMER。对于相同程度的并行性,我们提供了5倍和15倍的加速改进,分别比FPGA和GPU。对于同样尺寸的硅,优势又增加了10倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Coarse Grain Reconfigurable Architecture for sequence alignment problems in bio-informatics
A Coarse Grain Reconfigurable Architecture (CGRA) tailored for accelerating bio-informatics algorithms is proposed. The key innovation is a light weight bio-informatics processor that can be reconfigured to perform different Add Compare and Select operations of the popular sequencing algorithms. A programmable and scalable architectural platform instantiates an array of such processing elements and allows arbitrary partitioning and scheduling schemes and capable of solving complete sequencing algorithms including the sequential phases and deal with arbitrarily large sequences. The key difference of the proposed CGRA based solution compared to FPGA and GPU based solutions is a much better match of the architecture and algorithm for the core computational need as well as the system level architectural need. This claim is quantified for three popular sequencing algorithms: the Needleman-Wunsch, Smith-Waterman and HMMER. For the same degree of parallelism, we provide a 5 X and 15 X speed-up improvements compared to FPGA and GPU respectively. For the same size of silicon, the advantage grows by a factor of another 10 X.
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