Department of Chemistry, Imperial College London, London, UK.
Centre of Excellence in Neurotechnology, Imperial College London, London, UK.
Nat Methods. 2024 Feb;21(2):322-330. doi: 10.1038/s41592-023-02138-w. Epub 2024 Jan 18.
The development of high-resolution microscopes has made it possible to investigate cellular processes in 3D and over time. However, observing fast cellular dynamics remains challenging because of photobleaching and phototoxicity. Here we report the implementation of two content-aware frame interpolation (CAFI) deep learning networks, Zooming SlowMo and Depth-Aware Video Frame Interpolation, that are highly suited for accurately predicting images in between image pairs, therefore improving the temporal resolution of image series post-acquisition. We show that CAFI is capable of understanding the motion context of biological structures and can perform better than standard interpolation methods. We benchmark CAFI's performance on 12 different datasets, obtained from four different microscopy modalities, and demonstrate its capabilities for single-particle tracking and nuclear segmentation. CAFI potentially allows for reduced light exposure and phototoxicity on the sample for improved long-term live-cell imaging. The models and the training and testing data are available via the ZeroCostDL4Mic platform.
高分辨率显微镜的发展使得研究细胞在三维空间和随时间的过程成为可能。然而,由于光漂白和光毒性,观察快速细胞动力学仍然具有挑战性。在这里,我们报告了两个基于内容感知的帧插值(CAFI)深度学习网络的实现,即 Zooming SlowMo 和 Depth-Aware Video Frame Interpolation,它们非常适合准确预测图像对之间的图像,从而提高图像序列采集后的时间分辨率。我们表明,CAFI 能够理解生物结构的运动上下文,并能比标准插值方法表现得更好。我们在来自四种不同显微镜模式的 12 个不同数据集上对 CAFI 的性能进行了基准测试,并展示了其在单粒子跟踪和核分割方面的能力。CAFI 有可能减少对样本的光暴露和光毒性,从而改善长期活细胞成像。模型和训练及测试数据可通过 ZeroCostDL4Mic 平台获得。