RAiSD-X

Nikolaos S. Alachiotis, Charalampos Vatsolakis, Grigorios Chrysos, D. Pnevmatikatos
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Abstract

Detecting traces of positive selection in genomes carries theoretical significance and has practical applications from shedding light on the forces that drive adaptive evolution to the design of more effective drug treatments. The size of genomic datasets currently grows at an unprecedented pace, fueled by continuous advances in DNA sequencing technologies, leading to ever-increasing compute and memory requirements for meaningful genomic analyses. The majority of existing methods for positive selection detection either are not designed to handle whole genomes or scale poorly with the sample size; they inevitably resort to a runtime versus accuracy tradeoff, raising an alarming concern for the feasibility of future large-scale scans. To this end, we present RAiSD-X, a high-performance system that relies on a decoupled access-execute processing paradigm for efficient FPGA acceleration and couples a novel, to our knowledge, sliding-window algorithm for the recently introduced μ statistic with a mutation-driven hashing technique to rapidly detect patterns in the data. RAiSD-X achieves up to three orders of magnitude faster processing than widely used software implementations, and more importantly, it can exhaustively scan thousands of human chromosomes in minutes, yielding a scalable full-system solution for future studies of positive selection in species of flora and fauna.
RAiSD-X
检测基因组中积极选择的痕迹具有理论意义,并具有从揭示驱动适应性进化的力量到设计更有效的药物治疗的实际应用。在DNA测序技术不断进步的推动下,基因组数据集的规模目前以前所未有的速度增长,导致有意义的基因组分析对计算和内存的需求不断增加。大多数现有的阳性选择检测方法要么不是为处理全基因组而设计的,要么与样本量的比例很差;它们不可避免地需要在运行时和精度之间进行权衡,这引起了人们对未来大规模扫描可行性的担忧。为此,我们提出了一种高性能系统RAiSD-X,它依赖于解耦的访问-执行处理范式来实现高效的FPGA加速,并将我们所知的用于最近引入的μ统计量的滑动窗口算法与突变驱动哈希技术相结合,以快速检测数据中的模式。与广泛使用的软件相比,RAiSD-X的处理速度快了三个数量级,更重要的是,它可以在几分钟内彻底扫描数千条人类染色体,为未来动植物物种的正选择研究提供可扩展的全系统解决方案。
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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