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Register a new userHigh Bandwidth Memory on FPGAs: A Data Analytics Perspective
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Added by
Kaan Kara
Publication date
2020
fields
Informatics Engineering
and research's language is
English
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FPGA-based data processing in datacenters is increasing in popularity due to the demands of modern workloads and the ensuing necessity for specialization in hardware. Driven by this trend, vendors are rapidly adapting reconfigurable devices to suit data and compute intensive workloads. Inclusion of High Bandwidth Memory (HBM) in FPGA devices is a recent example. HBM promises overcoming the bandwidth bottleneck, faced often by FPGA-based accelerators due to their throughput oriented design. In this paper, we study the usage and benefits of HBM on FPGAs from a data analytics perspective. We consider three workloads that are often performed in analytics oriented databases and implement them on FPGA showing in which cases they benefit from HBM: range selection, hash join, and stochastic gradient descent for linear model training. We integrate our designs into a columnar database (MonetDB) and show the trade-offs arising from the integration related to data movement and partitioning. In certain cases, FPGA+HBM based solutions are able to surpass the highest performance provided by either a 2-socket POWER9 system or a 14-core XeonE5 by up to 1.8x (selection), 12.9x (join), and 3.2x (SGD).
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DNA sequencing is the physical/biochemical process of identifying the location of the four bases (Adenine, Guanine, Cytosine, Thymine) in a DNA strand. As semiconductor technology revolutionized computing, modern DNA sequencing technology (termed Next Generation Sequencing, NGS)revolutionized genomic research. As a result, modern NGS platforms can sequence hundreds of millions of short DNA fragments in parallel. The sequenced DNA fragments, representing the output of NGS platforms, are termed reads. Besides genomic variations, NGS imperfections induce noise in reads. Mapping each read to (the most similar portion of) a reference genome of the same species, i.e., read mapping, is a common critical first step in a diverse set of emerging bioinformatics applications. Mapping represents a search-heavy memory-intensive similarity matching problem, therefore, can greatly benefit from near-memory processing. Intuition suggests using fast associative search enabled by Ternary Content Addressable Memory (TCAM) by construction. However, the excessive energy consumption and lack of support for similarity matching (under NGS and genomic variation induced noise) renders direct application of TCAM infeasible, irrespective of volatility, where only non-volatile TCAM can accommodate the large memory footprint in an area-efficient way. This paper introduces GeNVoM, a scalable, energy-efficient and high-throughput solution. Instead of optimizing an algorithm developed for general-purpose computers or GPUs, GeNVoM rethinks the algorithm and non-volatile TCAM-based accelerator design together from the ground up. Thereby GeNVoM can improve the throughput by up to 113.5 times (3.6); the energy consumption, by up to 210.9 times (1.36), when compared to a GPU (accelerator) baseline, which represents one of the highest-throughput implementations known.
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