FPGA Accelerated INDEL Realignment in the Cloud

Lisa Wu, David Bruns-Smith, Frank A. Nothaft, Qijing Huang, S. Karandikar, Johnny Le, Andrew Lin, Howard Mao, B. Sweeney, K. Asanović, D. Patterson, A. Joseph
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引用次数: 33

Abstract

The amount of data being generated in genomics is predicted to be between 2 and 40 exabytes per year for the next decade, making genomic analysis the new frontier and the new challenge for precision medicine. This paper explores targeted deployment of hardware accelerators in the cloud to improve the runtime and throughput of immensescale genomic data analyses. In particular, INDEL (INsertion/DELetion) realignment is a critical operation that enables diagnostic testings of cancer through error correction prior to variant calling. It is the slowest part of the somatic (cancer) genomic analysis pipeline, the alignment refinement pipeline, and represents roughly one-third of the execution time of timesensitive diagnostics for acute cancer patients. To accelerate genomic analysis, this paper describes a hardware accelerator for INDEL realignment (IR), and a hardware-software framework leveraging FPGAs-as-a-service in the cloud. We chose to implement genomics analytics on FPGAs because genomic algorithms are still rapidly evolving (e.g. the de facto standard “GATK Best Practices” has had five releases since January of this year). We chose to deploy genomics accelerators in the cloud to reduce capital expenditure and to provide a more quantitative performance and cost analysis. We built and deployed a sea of IR accelerators using our hardware-software accelerator development framework on AWS EC2 F1 instances. We show that our IR accelerator system performed 81× better than multi-threaded genomic analysis software while being 32× more cost efficient. Keywords-Computer Architecture, Microarchitecture, Accelerator Architecture, Hardware Specialization, Genomic Analytics, INDEL Realignment, FPGA Acceleration, FPGAs-as-aservice, Cloud FPGAs
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FPGA加速云中的INDEL对齐
据预测,在未来十年,基因组学每年产生的数据量将在2到40艾字节之间,这使得基因组分析成为精准医疗的新前沿和新挑战。本文探讨了在云中有针对性地部署硬件加速器,以改善大规模基因组数据分析的运行时间和吞吐量。特别是,INDEL(插入/删除)重组是一项关键操作,可以在变体调用之前通过错误纠正来进行癌症诊断测试。它是体细胞(癌症)基因组分析管道(校准优化管道)中最慢的部分,大约占急性癌症患者时间敏感诊断执行时间的三分之一。为了加速基因组分析,本文描述了一个用于INDEL重组(IR)的硬件加速器,以及一个利用云端fpga即服务的硬件软件框架。我们选择在fpga上实现基因组分析,因为基因组算法仍在快速发展(例如,事实上的标准“GATK最佳实践”自今年1月以来已经发布了五个版本)。我们选择在云中部署基因组加速器,以减少资本支出,并提供更定量的性能和成本分析。我们在AWS EC2 F1实例上使用我们的硬件软件加速器开发框架构建并部署了大量IR加速器。我们的IR加速系统比多线程基因组分析软件性能好81倍,成本效率高32倍。关键词:计算机体系结构,微体系结构,加速器体系结构,硬件专业化,基因组分析,INDEL重新排列,FPGA加速,FPGA即服务,云FPGA
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