Design Space Exploration of Neural Network Activation Function Circuits

The widespread application of artificial neural networks has prompted researchers to experiment with FPGA and customized ASIC designs to speed up their computation. These implementation efforts have generally focused on weight multiplication and signal summation operations, and less on activation functions used in these applications. Yet, efficient hardware implementations of nonlinear activation functions like Exponential Linear Units (ELU), Scaled Exponential Linear Units (SELU), and Hyperbolic Tangent (tanh), are central to designing effective neural network accelerators, since these functions require lots of resources. In this paper, we explore efficient hardware implementations of activation functions using purely combinational circuits, with a focus on two widely used nonlinear activation functions, i.e., SELU and tanh. Our experiments demonstrate that neural networks are generally insensitive to the precision of the activation function. The results also prove that the proposed combinational circuit-based approach is very efficient in terms of speed and area, with negligible accuracy loss on the MNIST, CIFAR-10 and IMAGENET benchmarks. Synopsys Design Compiler synthesis results show that circuit designs for tanh and SELU can save between 3.13-7.69 and 4.45-8:45 area compared to the LUT/memory-based implementations, and can operate at 5.14GHz and 4.52GHz using the 28nm SVT library, respectively. The implementation is available at: https://github.com/ThomasMrY/ActivationFunctionDemo.Comment: 5 pages, 5 figures, 16 conferenc

Robust estimation of bacterial cell count from optical density

Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data