快速基因组分析利用精确的字符串匹配

Beatrice Branchini, Sofia Breschi, Alberto Zeni, M. Santambrogio
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引用次数: 2

摘要

基因组组装是生物信息学中最具挑战性的任务之一,因为它是许多应用的关键。基因组组装的基本任务之一是精确的序列比对。这个过程能够识别DNA内的复发模式和突变,这可以极大地支持临床医生提供更快的诊断和生产个体特异性药物。然而,这一过程代表了基因组分析的瓶颈,因为它是计算密集和耗时的。在这种情况下,所选算法执行此操作的效率对于加快分析过程也起着至关重要的作用。在本文中,我们提出了一种高性能,节能的FPGA实现KMP算法。我们的多核架构可以并行化序列的对齐过程,在保持高灵活性的同时显著减少了执行时间。实验结果表明,我们在Xilinx Alveo U280上的实现实现了高达2.68倍的加速和高达7.46倍的能效改进,而Bowtie2是在40线程英特尔至强处理器上运行的最先进的序列比对应用程序。最后,我们的设计在吞吐量和能源效率方面也分别比目前最先进的KMP硬件加速应用高出19.38倍和15.63倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fast Genome Analysis Leveraging Exact String Matching
Genome assembly is one of the most challenging tasks in bioinformatics, as it is the key to many applications. One of the fundamental tasks in genome assembly is exact sequence alignment. This process enables the identification of recurrent patterns and mutations inside the DNA, which can substantially support clinicians in providing a quicker diagnosis and producing individual-specific drugs. However, this procedure represents a bottleneck in genome analysis as it is computationally intensive and time-consuming. In this scenario, the efficiency of the chosen algorithm to perform this operation also plays a crucial role to speed up the analysis process. In this paper, we present a high-performance, energy-efficient FPGA implementation of the Knuth Morris Pratt (KMP) algorithm. Our multi-core architecture can parallelize the alignment procedure of the sequences, significantly reducing the execution time while still maintaining high flexibility. Experimental results show that our implementation on a Xilinx Alveo U280 achieves up to $2.68\times$ speedup and up to $7.46\times$ improvement in energy efficiency against Bowtie2, a State-of-the-Art application for sequence alignment run on a 40-thread Intel Xeon processor. Finally, our design also outperforms hardware-accelerated applications of the KMP present the State of the Art by up to $19.38\times$ and $15.63\times$ in terms of throughput and energy efficiency respectively.
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