Cell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
LaVision Biotec GmbH, Bielefeld, Germany.
Nat Commun. 2022 Jun 11;13(1):3362. doi: 10.1038/s41467-022-30907-2.
Modern implementations of widefield fluorescence microscopy often rely on sCMOS cameras, but this camera architecture inherently features pixel-to-pixel variations. Such variations lead to image artifacts and render quantitative image interpretation difficult. Although a variety of algorithmic corrections exists, they require a thorough characterization of the camera, which typically is not easy to access or perform. Here, we developed a fully automated pipeline for camera characterization based solely on thermally generated signal, and implemented it in the popular open-source software Micro-Manager and ImageJ/Fiji. Besides supplying the conventional camera maps of noise, offset and gain, our pipeline also gives access to dark current and thermal noise as functions of the exposure time. This allowed us to avoid structural bias in single-molecule localization microscopy (SMLM), which without correction is substantial even for scientific-grade, cooled cameras. In addition, our approach enables high-quality 3D super-resolution as well as live-cell time-lapse microscopy with cheap, industry-grade cameras. As our approach for camera characterization does not require any user interventions or additional hardware implementations, numerous correction algorithms that rely on camera characterization become easily applicable.
现代宽场荧光显微镜的实现通常依赖于 sCMOS 相机,但这种相机架构固有地具有像素到像素的变化。这种变化导致图像伪影,并使定量图像解释变得困难。尽管存在各种算法校正方法,但它们需要对相机进行彻底的特性描述,而通常不容易访问或执行。在这里,我们开发了一种完全基于热信号的相机特性描述自动化流水线,并将其在流行的开源软件 Micro-Manager 和 ImageJ/Fiji 中实现。除了提供传统的噪声、偏移和增益相机图外,我们的流水线还可以访问暗电流和热噪声作为曝光时间的函数。这使得我们能够避免单分子定位显微镜(SMLM)中的结构偏差,即使对于科学级别的冷却相机,这种偏差也很大。此外,我们的方法还可以实现高质量的 3D 超分辨率以及使用廉价的工业级相机进行活细胞延时显微镜。由于我们的相机特性描述方法不需要任何用户干预或额外的硬件实现,因此许多依赖于相机特性描述的校正算法变得易于应用。