Using video-oriented instructions to speed up sequence comparison.

A Wozniak
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引用次数: 166

Abstract

Motivation: This document presents an implementation of the well-known Smith-Waterman algorithm for comparison of proteic and nucleic sequences, using specialized video instructions. These instructions, SIMD-like in their design, make possible parallelization of the algorithm at the instruction level.

Results: Benchmarks on an ULTRA SPARC running at 167 MHz show a speed-up factor of two compared to the same algorithm implemented with integer instructions on the same machine. Performance reaches over 18 million matrix cells per second on a single processor, giving to our knowledge the fastest implementation of the Smith-Waterman algorithm on a workstation. The accelerated procedure was introduced in LASSAP--a LArge Scale Sequence compArison Package software developed at INRIA--which handles parallelism at higher level. On a SUN Enterprise 6000 server with 12 processors, a speed of nearly 200 million matrix cells per second has been obtained. A sequence of length 300 amino acids is scanned against SWISSPROT R33 (1,8531,385 residues) in 29 s. This procedure is not restricted to databank scanning. It applies to all cases handled by LASSAP (intra- and inter-bank comparisons, Z-score computation, etc.

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使用面向视频的指令来加快序列比较。
动机:本文件提出了一个著名的史密斯-沃特曼算法的实现,用于比较蛋白质和核酸序列,使用专门的视频指令。这些指令在设计上类似simd,使算法在指令级上并行化成为可能。结果:运行在167 MHz的ULTRA SPARC上的基准测试显示,与在同一台机器上使用整数指令实现的相同算法相比,加速因子是两倍。在单个处理器上的性能达到每秒超过1800万个矩阵单元,据我们所知,这是Smith-Waterman算法在工作站上最快的实现。加速程序是在LASSAP中引入的,LASSAP是由INRIA开发的大规模序列比较软件包软件,用于处理更高级别的并行性。在具有12个处理器的SUN Enterprise 6000服务器上,获得了每秒近2亿个矩阵单元的速度。全长300个氨基酸的序列在29 s内被SWISSPROT R33(1,8531,385个残基)扫描。此程序并不局限于数据库扫描。它适用于LASSAP处理的所有情况(银行内部和银行间比较,z分数计算等)。
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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A genetic algorithm for multiple molecular sequence alignment. Displaying the information contents of structural RNA alignments: the structure logos. Q-RT-PCR: data analysis software for measurement of gene expression by competitive RT-PCR. SS3D-P2: a three dimensional substructure search program for protein motifs based on secondary structure elements. XDOM, a graphical tool to analyse domain arrangements in any set of protein sequences.
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