Evidence map›Paper›PMID 41360790›Full record

ArticleNature communications2025

Volumetric localization microscopy with deep learning.

Keyi Han, Xuanwen Hua, Tianrui Qi, Zijun Gao, Xiaopeng Wang, Shu Jia

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. LFC-Lab on a chip · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Keyi Han *Laboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA.ORCID http://orcid.org/0000-0002-5141-1673
Xuanwen Hua *Laboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA.ORCID http://orcid.org/0000-0002-5946-0808
Tianrui Qi *Laboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA.ORCID http://orcid.org/0000-0002-8601-3691
Zijun GaoLaboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA.ORCID http://orcid.org/0000-0002-8583-3364
Xiaopeng WangLaboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA.
Shu JiaLaboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA. shu.jia@gatech.edu.ORCID http://orcid.org/0000-0001-6854-7537

Funding

Toward Systems Biophotonics: Imaging Biology across High Dimensions and ScalesR35GM124846 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI Shu Jia · 2017 to 2026
$4.0M
Functional screen for genetic causes of hypoplastic left heart syndromeR21HD110918 · NICHD · GEORGIA INSTITUTE OF TECHNOLOGY · PI JIA, SHU, NIE, SHUYI · 2023 to 2024
$391k
National Science Foundation (NSF) 2145235National Science Foundation (NSF) EFMA1830941NICHD NIH HHS R21 HD110918NIGMS NIH HHS R35 GM124846U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35GM124846
6 · The paper itself

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.

Indexed as

Deep LearningImaging, Three-DimensionalMicroscopySingle Molecule ImagingAlgorithmsAnimalsHumansImage Processing, Computer-AssistedMicroscopy, FluorescenceNeural Networks, Computer

Identifiers

PMID41360790
PMCPMC12686016

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.