Tile optimization for area in FPGA based hardware acceleration of peptide identification

S. Vidanagamachchi, S. Dewasurendra, R. Ragel, M. Niranjan
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引用次数: 10

Abstract

Advances in life sciences over the last few decades have lead to the generation of a huge amount of biological data. Computing research has become a vital part in driving biological discovery where analysis and categorization of biological data are involved. String matching algorithms can be applied for protein/gene sequence matching and with the phenomenal increase in the size of string databases to be analyzed, software implementations of these algorithms seems to have hit a hard limit and hardware acceleration is increasingly being sought. Several hardware platforms such as Field Programmable Gate Arrays (FPGA), Graphics Processing Units (GPU) and Chip Multi Processors (CMP) are being explored as hardware platforms. In this paper, we give a comprehensive overview of the literature on hardware acceleration of string matching algorithms, we take an FPGA hardware exploration and expedite the design time by a design automation technique. Further, our design automation is also optimized for better hardware utilization through optimizing the number of peptides that can be represented in an FPGA tile. The results indicate significant improvements in design time and hardware utilization which are reported in this paper.
基于FPGA的区域优化多肽识别硬件加速
在过去的几十年里,生命科学的进步导致了大量生物数据的产生。计算研究已成为推动生物发现的重要组成部分,其中涉及生物数据的分析和分类。字符串匹配算法可以应用于蛋白质/基因序列匹配,随着要分析的字符串数据库规模的显著增加,这些算法的软件实现似乎已经达到了硬极限,越来越多的人寻求硬件加速。现场可编程门阵列(FPGA)、图形处理单元(GPU)和芯片多处理器(CMP)等硬件平台正在被探索作为硬件平台。在本文中,我们对字符串匹配算法硬件加速的文献进行了全面的概述,我们进行了FPGA硬件探索,并通过设计自动化技术加快了设计时间。此外,我们的设计自动化还通过优化可在FPGA中表示的肽的数量来优化更好的硬件利用率。结果表明,在设计时间和硬件利用率方面有显著的改进。
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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