ArticleNature communications2025
Volumetric localization microscopy with deep learning.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- LFC-Lab on a chip · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Super-resolution microscopy, particularly localization-based methods, necessitates careful balancing of optical complexity, computational demands, and user accessibility. Conventional strategies typically adopt either deterministic or learning-based approaches, overlooking opportunities to leverage their synergistic strengths. In this work, we introduce volumetric localization microscopy (VLM) with deep learning, a super-resolution methodology that integrates instrumental and algorithmic advancements for high-fidelity 3D single-molecule imaging. VLM employs a wavefront-optimized light-field configuration to capture single-molecule data, while a cascaded neural network reconstructs 3D volumes and extracts molecular coordinates at a 10 nm lateral and 25 nm axial localization precision with effective imaging depth over 4 µm. Unlike existing methods, VLM is trained exclusively with system-aware intrinsic point-spread functions, bypassing dependencies on external imaging modalities or sample-specific data training. We validate VLM across diverse biological specimens, demonstrating hardware simplicity, data efficiency, and minimal phototoxicity. We anticipate VLM will overcome current limitations in fluorescence microscopy, empowering broader advancements in biomedical research.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.