An optical flow tool, called OpticalFlow3D, that can be run in Python or MATLAB and is compatible with three-dimensional microscopy images is described, to illustrate how OpticalFlow3D can enable new biological insight.
Abstract
ABSTRACT Motion is an essential component of any living system. It is rich with information, but it is often challenging to quantitatively extract biologically informative results from the motion apparent in microscopy images. This challenge is exacerbated by the wide variety in biological movement, which often takes the form of difficult-to-segment amorphous structures undergoing complex motion. An image processing technique known as optical flow can capture motion at each pixel in an image, thus bypassing the need for object segmentation or prior definition of motion types. This makes it a powerful tool for quantitative assessment of biological systems from the protein to organism scale. However, despite its flexibility and strengths for analyzing fluorescence microscopy images, its adoption in the bioimaging community has been limited by the availability of easy-to-use tools and guidance in results interpretation. Here, we describe an optical flow tool, called OpticalFlow3D, that can be run in Python or MATLAB and is compatible with three-dimensional microscopy images. Using biological examples across length scales, we illustrate how OpticalFlow3D can enable new biological insight.
One-step nanoscale ExM is developed, which combines ExM with fluctuation-based super-resolution analysis to enable the direct visualization of individual protein shapes, using conventional fluorescence microscopes, a capability that was previously limited to cryo-electron microscopy and averaging-based techniques.
Ali H. Shaib, Mohamad Mahdi Alawieh, S. Rizzoli· Nature Protocols· 0 citations
The capabilities of napari-lattice are demonstrated by quantifying cellular dynamics of human blood neutrophils using an LLSM and how napari-lattice can be used with publicly available oblique plane microscopy (OPM) datasets of different configurations.
P. Rajasekhar, Michael Milton, N. Geoghegan et al.· Journal of Microscopy· 0 citations
Fully capturing the heterogeneity of biological processes remains a central challenge, as conventional confocal microscopy typically surveys large ensembles of molecules within a small volume. The development of super-resolution imaging enables the capture of images with exceptional detail. When super-resolution is com...
Wonsang Hwang, Bing-Ying Zhao, Kai Guo et al.· Science Advances· 0 citations
These results show that virtual staining can move from offline post-processing to a real-time microscopy capability, and integration into a Napari-based interface demonstrates its practical utility in interactive imaging scenarios.
Shao-Wei Chen, Yun-Fei Zhang, Jun-Hao Lin et al.· Global Intelligent Industry...· 0 citations
In vivo imaging of dynamic subcellular brain structures is key to understanding several phenomena in neuroscience. However, in the fruit fly, its implementation has been hindered by a trade-off among spatial resolution, speed, photobleaching, phototoxicity, and setup complexity required to access specific target regi...
Francisco J. Tassara, M. Barella, Tomás Sebastián Fernández Troncoso et al.· ACS Photonics· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.