首页> 外文会议>2019 56th ACM/IEEE Design Automation Conference >AlignS: A Processing-In-Memory Accelerator for DNA Short Read Alignment Leveraging SOT-MRAM
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AlignS: A Processing-In-Memory Accelerator for DNA Short Read Alignment Leveraging SOT-MRAM

机译:AlignS:利用SOT-MRAM进行DNA短读比对的内存中处理加速器

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摘要

Classified as a complex big data analytics problem, DNA short read alignment serves as a major sequential bottleneck to massive amounts of data generated by next-generation sequencing platforms. With Von-Neumann computing architectures struggling to address such computationally-expensive and memory-intensive task today, Processing-in-Memory (PIM) platforms are gaining growing interests. In this paper, an energy-efficient and parallel PIM accelerator (AlignS) is proposed to execute DNA short read alignment based on an optimized and hardware-friendly alignment algorithm. We first develop AlignS’s platform that harnesses SOT-MRAM as computational memory and transforms it to a fundamental processing unit for short read alignment. Accordingly, we present a novel, customized, highly parallel read alignment algorithm that only seeks the proposed simple and parallel in-memory operations (i.e. comparisons and additions). AlignS is then optimized through a new correlated data partitioning and mapping methodology that allows local storage and processing of DNA sequence to fully exploit the algorithm-level’s parallelism, and to accelerate both exact and inexact matches. The device-to-architecture co-simulation results show that AlignS improves the short read alignment throughput per Watt per mm2 by ~12× compared to the ASIC accelerator. Compared to recent FM-index-based ReRAM platform, AlignS achieves 1.6× higher throughput per Watt.
机译:DNA短读比对被归类为复杂的大数据分析问题,是下一代测序平台生成的大量数据的主要顺序瓶颈。如今,由于冯·诺依曼(Von-Neumann)计算体系结构努力解决这样的计算昂贵和内存密集型任务,内存处理(PIM)平台越来越引起人们的关注。本文提出了一种节能高效的并行PIM加速器(AlignS),它基于优化且硬件友好的比对算法执行DNA短读比对。我们首先开发AlignS平台,该平台利用SOT-MRAM作为计算内存,并将其转换为基本的处理单元,以实现短读取对齐。因此,我们提出了一种新颖的,定制的,高度并行的读取对齐算法,该算法仅寻找所提出的简单且并行的内存中操作(即比较和加法)。然后,通过一种新的相关数据分区和映射方法对AlignS进行优化,该方法可以对DNA序列进行本地存储和处理,从而充分利用算法级的并行性,并加快精确和不精确的匹配。设备到体系结构的协同仿真结果表明,AlignS提高了每毫米每瓦的短读取对齐吞吐量\ n 2 \ n约12倍。与最近的基于FM索引的ReRAM平台相比,AlignS的每瓦吞吐量提高了1.6倍。

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