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Accelerated cell imaging and classification on FPGAs for quantitative-phase asymmetric-detection time-stretch optical microscopy

机译:FPGA上的加速细胞成像和分类,用于定量相非对称检测时间拉伸光学显微镜

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With the fundamental trade-off between speed and sensitivity, existing quantitative phase imaging (QPI) systems for diagnostics and cell classification are often limited to batch processing only small amount of offline data. While quantitative asymmetric-detection time-stretch optical microscopy (Q-ATOM) offers a unique optical platform for ultrafast and high-sensitivity quantitative phase cellular imaging, performing the computationally demanding backend QPI phase retrieval and image classification in real-time remains a major technical challenge. In this paper, we propose an optimized architecture for QPI on FPGA and compare its performance against CPU and GPU implementations in terms of speed and power efficiency. Results show that our implementation on single FPGA card demonstrates a speedup of 9.4 times over an optimized C implementation running on a 6-core CPU, and 3.47 times over the GPU implementation. It is also 24.19 and 4.88 times more power-efficient than the CPU and GPU implementation respectively. Throughput increase linearly when four FPGA cards are used to further improve the performance. We also demonstrate an increased classification accuracy when phase images instead of single-angle ATOM images are used. Overall, one FPGA card is able to process and categorize 2497 cellular images per second, making it suitable for real-time single-cell analysis applications.
机译:由于速度和灵敏度之间存在根本的折衷,因此现有的用于诊断和细胞分类的定量相位成像(QPI)系统通常仅限于批量处理少量离线数据。定量非对称检测时延光学显微镜(Q-ATOM)为超快速和高灵敏度定量相细胞成像提供了独特的光学平台,但实时执行对计算要求苛刻的后端QPI相位检索和图像分类仍然是一项主要技术挑战。在本文中,我们提出了一种针对FPGA上QPI的优化架构,并在速度和功耗效率方面将其性能与CPU和GPU的实现进行了比较。结果表明,我们在单个FPGA卡上的实现比在6核CPU上运行的优化C实现的速度提高了9.4倍,比GPU实现的速度提高了3.47倍。它的能效分别比CPU和GPU实现高24.19和4.88倍。当使用四个FPGA卡进一步提高性能时,吞吐量线性增加。当使用相位图像而不是单角度ATOM图像时,我们还证明了分类精度的提高。总体而言,一张FPGA卡每秒能够处理和分类2497个蜂窝图像,使其适合于实时单细胞分析应用。

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