DP2: A Highly Parallel Range Join for Genome Analysis on Distributed Computing Platform

Aman Sinha, B. Lai
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Abstract

Rapid growth of the sheer amount of genome data and intense computation become great challenges for downstream genome analytics. Efficient parallel processing and distributed computing are the two effective schemes to address the analysis of big data. Range join is a widely used, effective, yet time-consuming operation that finds the overlap between two different sets of genome features. The current widely adopted BEDTools [6] pipeline adopts single-node binary tree approach, while the distributed GenAp scheme fails to exploit the massive parallel computation on modern throughput processors, such as GPU (Graphic Processing Unit). This paper proposes a novel Distributed Parallel P-ary search (DP2) that applies novel P-ary analysis to enable high parallelism at algorithmic level, and extensively utilize multiple GPUs at system and architecture level. Efficient computation allocation is implemented to leverage the distributed computing on clusters. The proposed framework can be well integrated with current BEDTools [6] pipeline, and achieves an average of 25x speedup for the actual range-join operation when compared with Binary tree approach of GenAp and a 13x end-to-end (total execution time) speedup in comparison to ADAM.
分布式计算平台上基因组分析的高度并行范围连接DP2
基因组数据量的快速增长和密集的计算成为下游基因组分析的巨大挑战。高效并行处理和分布式计算是解决大数据分析的两种有效方案。范围连接是一种广泛使用,有效但耗时的操作,用于发现两组不同基因组特征之间的重叠。目前广泛采用的BEDTools[6]管道采用单节点二叉树方法,而分布式GenAp方案无法利用GPU (Graphic Processing Unit)等现代吞吐量处理器上的大规模并行计算。本文提出了一种新型的分布式并行p元搜索(DP2),它采用新颖的p元分析来实现算法级的高并行性,并在系统和架构级广泛利用多个gpu。实现高效的计算分配,充分利用集群上的分布式计算。所提出的框架可以很好地与当前的BEDTools[6]管道集成,与GenAp的二叉树方法相比,实际范围连接操作的平均加速速度提高了25倍,与ADAM相比,端到端(总执行时间)加速速度提高了13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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