Evidence map›Paper›PMID 41648204›Full record

ArticlebioRxiv : the preprint server for biology2026

Enhancing volumetric microscopy with blind computational correction of spatially variant aberrations using neural field representation.

Linh Hoang, Zhongqiang Li, Dominique Meyer, Xiankun Lu, Ji Yi

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Linh HoangDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore MD, 21231.ORCID 0000-0002-7764-3915
Zhongqiang LiDepartment of Ophthalmology, School of Medicine, Johns Hopkins University, Baltimore MD, 21231.ORCID 0000-0001-6962-5146
Dominique MeyerDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore MD, 21231.ORCID 0000-0002-3240-5227
Xiankun LuDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore MD, 21231.ORCID 0009-0006-8768-8718
Ji YiDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore MD, 21231.ORCID 0000-0001-6583-7192

Funding

A novel method for volumetric oxygen mapping in living retinaR01EY032163 · NEI · JOHNS HOPKINS UNIVERSITY · PI YI, JI · 2021 to 2024
$2.0M
Mesoscopic microscopy for ultra-high speed and large-scale volumetric brain imagingR01EB034272 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI Ji Yi · 2023 to 2026
$1.9M
Advancing visible light optical coherence tomography in glaucoma detectionR01EY034607 · NEI · JOHNS HOPKINS UNIVERSITY · PI Ji Yi · 2023 to 2026
$1.9M
NEI NIH HHS R01 EY032163NEI NIH HHS R01 EY034607NIBIB NIH HHS R01 EB034272
6 · The paper itself

Abstract

Studying biological processes across multi-millimeter scales requires imaging systems that combine high spatial resolution with a large field of view (FOV). However, optical aberrations degrade image quality, particularly in large-FOV systems where distortions gradually worsen toward the periphery. Existing methods for correcting field-dependent aberrations are limited and often impractical. Hardware-based solutions such as adaptive optics demand additional components and sample manipulation, increasing system complexity and experimental burden. Computational approaches, while promising, typically rely on exhaustive point spread function (PSF) calibration or large training datasets, restricting their applicability. We introduce a self-supervised algorithm that simultaneously estimates spatially varying aberrations and reconstructs 3D sample structure from a single blurred image-without PSF calibration or training data. Our method was implemented on optically cleared mouse hippocampal neurons and cortical vasculature imaged with oblique plane microscopy (OPM), as well as in vivo mouse retinal vasculature captured with adaptive optics scanning laser ophthalmoscopy (AOSLO), where PSF calibration is infeasible. The algorithm predicts and corrects aberrations across multi-millimeter FOVs, enhances contrast in low signal-to-noise regions, and reveals critical structural details in neuronal and vascular systems that are obscured in raw images. This approach enables high-resolution, large-scale imaging without hardware modifications, expanding the accessibility of advanced microscopy techniques.

Identifiers

PMID41648204
PMCPMC12871265

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.