Deep Learning for Cell Segmentation of Large Multi-Channels Time-Series Data in the Amira™ Software

J. Giesebrecht
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Abstract

Quantitative live cell imaging has been widely used to study various dynamical processes in cell biology. Fluorescence microscopy, a popular imaging modality for live cell imaging, has been used to monitor the dynamics of specific molecules in live cells. However, the fluorescence live cell images are highly prone to noise, low contrast, and uneven illumination. These often lead to erroneous cell segmentation, hindering quantitative analyses of dynamical cellular processes.
Amira™软件中大型多通道时间序列数据的深度学习细胞分割
定量活细胞成像已广泛应用于研究细胞生物学中的各种动态过程。荧光显微镜是一种流行的活细胞成像方式,已被用于监测活细胞中特定分子的动力学。然而,荧光活细胞图像很容易产生噪声,对比度低,光照不均匀。这些常常导致错误的细胞分割,阻碍了动态细胞过程的定量分析。
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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