标题:Accelerating large-scale biological database search on Xeon Phi-based neo-heterogeneous architectures
作者:Lan, Haidong ;Liu, Weiguo ;Schmidt, Bertil ;Wang, Bingqiang
作者机构:[Lan, Haidong ;Liu, Weiguo ] School of Computer Science and Technology, Engineering Research Center of Digital Media Technology, Ministry of Education 更多
会议名称:IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2015
会议日期:9 November 2015 through 12 November 2015
来源:Proceedings - 2015 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2015
出版年:2015
页码:503-510
DOI:10.1109/BIBM.2015.7359735
关键词:dynamic programming; Knights Corner vector instructions; neo-heterogeneous architecture; sequence alignment; Smith-Waterman; Xeon Phi
摘要:In this paper we present new parallelization techniques for searching large-scale biological sequence databases with the Smith-Waterman algorithm on Xeon Phi-based neoheterogenous architectures. In order to make full use of the compute power of both the multi-core CPU and the many-core Xeon Phi hardware, we use a collaborative computing scheme as well as hybrid parallelism. At the CPU side, we employ SSE intrinsics and multi-threading to implement SIMD parallelism. At the Xeon Phi side, we use Knights Corner vector instructions to gain more data parallelism. We have presented two dynamic task distribution schemes (thread level and device level) in order to achieve better load balancing. Furthermore, a multi-threaded asynchronous scheme is used to overlap communication and computation between CPUs and Xeon Phis. Evaluations on real protein sequence databases show that our method achieves a peak overall performance up to 220 GCUPS on a neo-heterogeneous platform consisting of two Intel E5-2620 CPUs and two Intel Xeon Phi 7110P cards. It also exhibits good scalability in terms of database size and query length. Our implementation is available at: http://turbo0628.github.io/LSBDS/. © 2015 IEEE.
收录类别:EI;SCOPUS
Scopus被引频次:5
资源类型:会议论文;期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84962447614&doi=10.1109%2fBIBM.2015.7359735&partnerID=40&md5=0a9de17dce05c13f1079c1ea1a0393c0
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