ArticleNature methods2025
Dark-based optical sectioning assists background removal in fluorescence microscopy.
Article in Nature methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Rapid robust high-fidelity 3D neuronal extraction from multiview calcium imaging datasets.Nature methods · 2026Article
- Structured illumination microscopy for high SNR 3D imaging from millimeter-thick tissues to cellular dynamics.Innovation (Cambridge (Mass.)) · 2026Article
- Organelle-specific fluorescent probes for live imaging at the nanoscale.Science China. Life sciences · 2026Review
- Illuminating the Interface: In Situ Optical Insights Into Two-Electron ORR Pathways for HAdvanced materials (Deerfield Beach, Fla.) · 2026Review
- Super-Resolution Structured Illumination Microscopy to Study Endocytosis and Cellular Nanoparticle Uptake.ACS nano · 2026Review
- Voltage imaging with periodic structured illumination.Biomedical optics express · 2026Article
- Time-deterministic cryo-optical microscopy.Light, science & applications · 2025Article
- High-fidelity tissue super-resolution imaging achieved with confocalLight, science & applications · 2025Article
- Voltage Imaging with Periodic Structured Illumination.bioRxiv : the preprint server for biology · 2025Article
- Compressive Fourier-Domain Intensity Coupling (C-FOCUS) enables near-millimeter deep imaging in the intact mouse brain in vivo.Research square · 2025Article
- Capturing more than meets the eye.Nature methods · 2025Article
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Authors and funding
29 authors.
Funding
Abstract
In fluorescence microscopy, a persistent challenge is the defocused background that obscures cellular details and introduces artifacts. Here, we introduce Dark sectioning, a method inspired by natural image dehazing for removing backgrounds that leverages dark channel prior and dual frequency separation to provide single-frame optical sectioning. Unlike denoising or deconvolution, Dark sectioning specifically targets and removes out-of-focus backgrounds, stably improving the signal-to-background ratio by nearly 10 dB and structural similarity index measure of images by approximately tenfold. Dark sectioning was validated using wide-field, confocal, two/three-dimensional structured illumination and one/two-photon microscopy with high-fidelity reconstruction. We further demonstrate its potential to improve the segmentation accuracy in deep tissues, resulting in better recognition of neurons in the mouse brain and accurate assessment of nuclei in prostate lesions or mouse brain sections. Dark sectioning is compatible with many other microscopy modalities, including light-sheet and light-field microscopy, as well as processing algorithms, including deconvolution and super-resolution optical fluctuation imaging.
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