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Hardware-accelerated reconstruction of compressed neural signals based on inpainting

机译:基于尿漆的压缩神经信号的硬件加速重建

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In this paper the first low-latency architecture design and hardware implementation for structure-based inpainting to detect and complete isophotes in brain activity recording is presented. This novel mask-based compression and inpainting-based reconstruction methodology for correlated neural signals is especially important for the realization of implantable neural measurement systems (NMS) due to restrictions in terms of area and energy. The data compression is obtained by on/off controlling of the recording electrodes on implant side. The low-latency and parallel architecture design is based on a synchronous Moore-FSM for 16 bits inputs. It requires only 8 cycles to compute the inpainting-based detection and completion of isophotes. Because of the error-robust inpainting recovery procedure, small accuracy differences between the simulation and measurement results on a Xilinx DS312 Spartan-3E FPGA are negligible. The proposed hardware implementation on logical and physical 350nm CMOS reaches a clock frequency of 78.452 MHz, which leads to a throughput of 653 766 parallel inpainting-based isophote computations per second.
机译:本文提出了一种基于结构的批量来检测和完成大脑活动记录中的异常的第一种低延迟架构设计和硬件实现。对于相关的神经信号的这种基于新的基于掩模的压缩和染色的重建方法对于实现可植入的神经测量系统(NMS)尤为重要,因为在区域和能量方面的限制。通过在植入物侧的记录电极开/关控制来获得数据压缩。低延迟和并行架构设计基于同步MOORE-FSM,用于16位输入。它只需要8个周期来计算基于初始的检测和isophotes。由于难以稳健的批量恢复过程,Xilinx DS312 Spartan-3E FPGA上的模拟和测量结果之间的小精度差异可以忽略不计。逻辑和物理350nm CMO上所提出的硬件实现达到78.452 MHz的时钟频率,这导致每秒653 766个并行染色的机芯计算的吞吐量。

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