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首页> 外文期刊>IBRO Reports >Automated identification of neural cells in the multi-photon images using deep-neural networks
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Automated identification of neural cells in the multi-photon images using deep-neural networks

机译:使用深层神经网络自动识别多光子图像中的神经细胞

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摘要

Correlative super-resolution structured illumination microscopy combined with array tomography for high accuracy synapse detection Electron microscopy (EM) has been the gold standard method for synapse detection owing to its ultra-high spatial resolution. Despite three-dimensional tissue image acquisition with high res- olution is available with EM, however, overall procedure to image acquisition and analysis still remains challenging. In addition, mul- tiple labeling method for EM is extremely limited. On the other hand, fluorescence microscopy (FM) has been essential tool for bio- logical research. FM offers large field-of-view (FOV), high contrast, and multiple labeling combination. However, conventional opti- cal microscopy meets challenge, which is the diffraction limit. It makes FM does not provide sufficient spatial resolution for synapse detection.
机译:相关的超分辨率结构照明显微镜与阵列层析成像相结合,用于高精度突触检测电子显微镜(EM)由于其超高的空间分辨率而成为突触检测的金标准方法。尽管EM可以进行高分辨率的三维组织图像采集,但是,图像采集和分析的整个过程仍然具有挑战性。此外,用于EM的多种标记方法极为有限。另一方面,荧光显微镜(FM)已成为生物研究的重要工具。 FM提供大视野(FOV),高对比度和多种标记组合。然而,传统的光学显微镜遇到了挑战,这是衍射极限。这使得FM无法为突触检测提供足够的空间分辨率。

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