Sep 2026· Journal of Microscopy· 0 citations· 15 references
Medicine
TL;DR
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.
Abstract
Lattice light-sheet microscopy (LLSM) has revolutionised live-cell imaging with its ability to resolve sub-cellular detail with high spatiotemporal resolution and minimal phototoxicity. However, LLSM often generates large terabyte-scale datasets that require complex preprocessing, creating bottlenecks in storage, data handling and analysis. These challenges are not unique to LLSM but also apply to oblique plane microscopy (OPM). To bridge this gap and reduce the time from large raw data acquisition to biological insight we developed napari-lattice, an open-source tool designed for scalable and modular LLSM workflows. napari-lattice provides a graphical user interface (GUI) for visualisation and analysis, and a command-line interface optimised for High-Performance Computing (HPC) environments. In this article, we demonstrate the capabilities of napari-lattice by quantifying cellular dynamics of human blood neutrophils using an LLSM. Data preprocessing and image analysis were combined into an end-to-end pipeline that used ilastik for cell segmentation and scikit-image for measuring cell morphology and intensity over time. This pipeline was then parallelised over regions of interest (ROIs) on an HPC node using napari-lattice. Restricting the analysis to ROIs reduced the deskewed data size ∼2.6-fold, allowing the full analysis pipeline to complete in ∼12 h, compared to the full field-of-view processing, which did not finish within 48 h. We also demonstrate how napari-lattice can be used with publicly available oblique plane microscopy (OPM) datasets of different configurations. Together, napari-lattice streamlines LLSM data analysis and visualisation, making analysis of complex, feature-rich datasets more accessible. This empowers researchers to fully leverage the potential of LLSM and OPM data.
Lattice light-sheet microscopy (LLSM) enables gentle, rapid, volumetric fluorescence imaging of living biological systems. The technique employs Bessel beam interference to produce a light-sheet which retains its thickness over a relatively large field-of-view compared to other light-sheets. In the decade since its com...
Helena L. E. Coker, David S. Corcoran· Journal of Microscopy· 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
Volumetric microscopy produces datasets too large to share as files and too rich to convey as still images, yet exploring them interactively means installing desktop software or building web infrastructure. Here we present Luxar, an open-source Python framework that compiles multidimensional data into compact archives...
Modern transmission electron microscopes are versatile instruments which have become indispensable tools for understanding structure and chemical composition at the nano- and atomic scale. In the physical sciences these instruments are still largely manually controlled, requiring significant operator expertise, limitin...
M. Danaie, M. England, Yi-Ming Xu et al.· 0 citations
3D-MAESTRO is applied to lightsheet images of whole mouse brains in the context of diverse anatomical and functional experiments, illustrating high-throughput and reproducible mapping of microscopic structures across the brain.
Camilo Laiton, Nicholas A. Lusk, Yoni Browning et al.· bioRxiv· 0 citations
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
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