Fast confocal microscopy imaging based on deep learning

Xiu Li, J. Dong, Bowen Li, Yi Zhang, Yongbing Zhang, A. Veeraraghavan, Xiangyang Ji
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引用次数: 6

Abstract

Confocal microscopy is the de-facto standard technique in bio-imaging for acquiring 3D images in the presence of tissue scattering. However, the point-scanning mechanism inherent in confocal microscopy implies that the capture speed is much too slow for imaging dynamic objects at sufficient spatial resolution and signal to noise ratio(SNR). In this paper, we propose an algorithm for super-resolution confocal microscopy that allows us to capture high-resolution, high SNR confocal images at an order of magnitude faster acquisition speed. The proposed Back-Projection Generative Adversarial Network (BPGAN) consists of a feature extraction step followed by a back-projection feedback module (BPFM) and an associated reconstruction network, these together allow for super-resolution of low-resolution confocal scans. We validate our method using real confocal captures of multiple biological specimens and the results demonstrate that our proposed BPGAN is able to achieve similar quality to high-resolution confocal scans while the imaging speed can be up to 64 times faster.
基于深度学习的快速共聚焦显微镜成像
共聚焦显微镜是事实上的标准技术,在生物成像获得三维图像的存在组织散射。然而,共聚焦显微镜固有的点扫描机制意味着,在足够的空间分辨率和信噪比(SNR)下,对动态物体成像的捕获速度太慢。在本文中,我们提出了一种超分辨率共聚焦显微镜算法,使我们能够以更快的采集速度捕获高分辨率,高信噪比的共聚焦图像。提出的反投影生成对抗网络(BPGAN)包括一个特征提取步骤,然后是一个反投影反馈模块(BPFM)和一个相关的重建网络,这些共同允许低分辨率共聚焦扫描的超分辨率。我们使用多个生物标本的真实共聚焦捕获验证了我们的方法,结果表明,我们提出的BPGAN能够达到与高分辨率共聚焦扫描相似的质量,而成像速度可以快64倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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