A Scalable Parallel Algorithm for Large-Scale Protein Sequence Homology Detection

Changjun Wu, A. Kalyanaraman, W. Cannon
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引用次数: 4

Abstract

Protein sequence homology detection is a fundamental problem in computational molecular biology, with a pervasive application in nearly all analyses that aim to structurally and functionally characterize protein molecules. While detecting homology between two protein sequences is computationally inexpensive, detecting pairwise homology at a large-scale becomes prohibitive, requiring millions of CPU hours. Yet, there is currently no efficient method available to parallelize this kernel. In this paper, we present the key characteristics that make this problem particularly hard to parallelize, and then propose a new parallel algorithm that is suited for large-scale protein sequence data. Our method, called pGraph, is designed using a hierarchical multiple-master multiple-worker model, where the processor space is partitioned into subgroups and the hierarchy helps in ensuring the workload is load balanced fashion despite the inherent irregularity that may originate in the input. Experimental evaluation demonstrates that our method scales linearly on all input sizes tested (up to 640K sequences) on a 1,024 node supercomputer. In addition to demonstrating strong scaling, we present an extensive study of the various components of the system and related parametric studies.
大规模蛋白质序列同源性检测的可扩展并行算法
蛋白质序列同源性检测是计算分子生物学中的一个基本问题,在几乎所有旨在对蛋白质分子进行结构和功能表征的分析中都有广泛的应用。虽然检测两个蛋白质序列之间的同源性在计算上不昂贵,但大规模检测成对同源性变得令人望而却步,需要数百万CPU小时。然而,目前还没有有效的方法来并行化这个内核。在本文中,我们提出了使该问题特别难以并行化的关键特征,然后提出了一种适合大规模蛋白质序列数据的新的并行算法。我们的方法称为pGraph,它是使用分层多主多工作者模型设计的,其中处理器空间被划分为子组,分层结构有助于确保工作负载以负载均衡的方式运行,尽管输入中可能存在固有的不规则性。实验评估表明,我们的方法在1024节点超级计算机上测试的所有输入大小(高达640K序列)上呈线性扩展。除了证明强尺度,我们提出了系统的各个组成部分和相关参数研究的广泛研究。
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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