Acceleration of the long read mapping on a PC-FPGA architecture (abstract only)

Peng Chen, Chao Wang, Xi Li, Xuehai Zhou
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引用次数: 3

Abstract

The genome sequence alignment, whereby ultra scale of sequence reads should be compared to an enormous long reference, has been one central challenge to the biologists for a long period. For recent years, new sequencing technology makes it possible to generate longer reads (sequences of genome fragments) which seem more valuable for the life science research. It has been foreseen that long genome reads (length longer than 200 base pairs) will dominate the field in the near future. Unfortunately, most of the state-of-art aligners nowadays are optimized and only applicable for the short read mapping while present long read aligners are still not satisfying at the aspect of speed. In this paper, we propose a novel PC-FPGA hybrid system to improve the performance of the long read mapping. The BWA-SW algorithm is chosen as the alignment approach and by accelerating the bottleneck of the algorithm, our solution could archive a significant improvement in term of speed. Experiments demonstrate that the described system is as accurate as the BWA-SW aligner and about 1.41-2.73 times faster than it for reads with lengths ranging from 500bp to 2000bp.
PC-FPGA架构下长读映射的加速(仅摘要)
长期以来,基因组序列比对一直是生物学家面临的一个核心挑战,即超大规模的序列读数应该与巨大的长参考文献相比较。近年来,新的测序技术使得生成较长的基因组片段序列成为可能,这在生命科学研究中显得更有价值。可以预见,在不久的将来,长基因组读取(长度超过200个碱基对)将主导该领域。遗憾的是,目前大多数的定位器都是经过优化的,只适用于短读映射,而现有的长读定位器在速度方面还不能令人满意。在本文中,我们提出了一种新的PC-FPGA混合系统来提高长读映射的性能。选择BWA-SW算法作为对齐方法,通过加速算法的瓶颈,我们的解决方案可以在速度方面得到显着提高。实验表明,该系统的精度与BWA-SW比对器相当,对于长度为500bp至2000bp的读取,其速度是BWA-SW比对器的1.41-2.73倍。
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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