GEM: A Framework for Developing Shared-Memory Parallel Genomic Applications on Memory Constrained Architectures

Mucahid Kutlu, G. Agrawal
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引用次数: 1

Abstract

Amount of available genomic data is increasing rapidly with the recent developments in sequencing technologies. Analysis of such data can potentially lead significant advancements in medical research and even practice. However, it is imperative to exploit parallelism and utilize computational resources effectively to handle large scale genomic data. At the same time, the trends in computing technologies are towards architectures with large number of cores and smaller memory size per core (e.g. Intel Xeon Phi). Innovative solutions that meet the requirements of parallel genomic data processing with the constraints of the new computational architectures are urgently needed. In this work, we develop a novel middleware system, GEM, for developing shared-memory parallel genomic applications with memory constraint architectures. We propose load-map-reduce approach and a novel scheduling scheme to decrease I/O contention and prevent over-consumption of the limited memory. We also use domain specific knowledge to decrease the memory requirements of the tasks. In our experiments, we show that GEM has high scalability on Intel Xeon Phi architecture. We also compare GEM against two other frameworks for genomic data processing, GATK and PAGE, and show that our middleware outperforms both.
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GEM:在内存受限架构上开发共享内存并行基因组应用的框架
随着测序技术的发展,可用的基因组数据量正在迅速增加。对这些数据的分析有可能在医学研究甚至实践方面取得重大进展。然而,利用并行性和有效利用计算资源来处理大规模基因组数据是势在必行的。与此同时,计算技术的发展趋势是拥有大量核心和更小的每核内存大小的架构(例如Intel Xeon Phi)。在新的计算架构的约束下,迫切需要满足并行基因组数据处理要求的创新解决方案。在这项工作中,我们开发了一个新的中间件系统GEM,用于开发具有内存约束架构的共享内存并行基因组应用程序。为了减少I/O争用和防止有限内存的过度消耗,我们提出了一种新的负载映射减少方法和调度方案。我们还使用特定领域的知识来减少任务的内存需求。在我们的实验中,我们证明GEM在Intel Xeon Phi架构上具有很高的可扩展性。我们还将GEM与另外两个基因组数据处理框架GATK和PAGE进行了比较,并表明我们的中间件优于两者。
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