Evidence map›Paper›PMID 41783388›Full record

ArticleJournal of biomedical optics2026

Improved 3D image reconstruction via deep-learning-based fusion of light-field microscopy and Fourier light-field microscopy images.

Er Ouyang, Liang Liang, Xuhui Zhou, Lin Zhao, Hui Fang

Abstract read
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Article in Journal of biomedical optics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Er OuyangShenzhen University, Institute of Microscale Optoelectronics and Shenzhen Key Laboratory of Microscale Optical Information Technology, Nanophotonics Research Center, Shenzhen, China.ORCID https://orcid.org/0000-0001-6350-3244
Liang LiangShenzhen University, Institute of Microscale Optoelectronics and Shenzhen Key Laboratory of Microscale Optical Information Technology, Nanophotonics Research Center, Shenzhen, China.
Xuhui ZhouShenzhen University, Institute of Microscale Optoelectronics and Shenzhen Key Laboratory of Microscale Optical Information Technology, Nanophotonics Research Center, Shenzhen, China.
Lin ZhaoHunan Institute of Science and Technology, Yueyang, China.
Hui FangShenzhen University, Institute of Microscale Optoelectronics and Shenzhen Key Laboratory of Microscale Optical Information Technology, Nanophotonics Research Center, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significance: Light-field microscopy (LFM) is a scanning-free 3D imaging technique that is useful for observing dynamic biological systems due to its unique capability to capture both spatial and angular information from samples in a single exposure. However, LFM suffers from the spatial-angular information trade-off associated with microlens arrays, and its spatial resolution is usually unsatisfactory for fine-structure imaging. Aim: To overcome this bottleneck, we introduce a deep-learning-based image fusion technique that combines LFM images with Fourier LFM (FLFM) images. The high spatial resolution of FLFM is combined with the dense angular acquisition capability of LFM to improve 3D image reconstruction quality. Approach: The deep learning network was trained with LFM, FLFM, and epipolar plane image data. The proposed neural network employs specialized feature extraction modules for each modality, with a U-Net backbone for 3D reconstruction, and integrates a hierarchical cascade-based result-level fusion strategy to jointly optimize multimodal features. This approach significantly enhances detail preservation and depth recovery in the final output. Results: Results obtained using a publicly available dataset of synthetic tubulins demonstrate that the proposed method outperforms state-of-the-art techniques. Quantitatively, it achieved a peak signal-to-noise ratio (PSNR) of 38.4729 and a structural similarity index measure (SSIM) of 0.9876, significantly outperforming both traditional algorithms and single-modality deep learning approaches. Furthermore, validation on a mouse brain blood vessels dataset confirms the effectiveness of the method in reconstructing biological structures, achieving a PSNR of 35.0548 and an SSIM of 0.8424. Conclusions: We introduce an approach that combines LFM with FLFM, providing an efficient and reliable solution for practical LFM applications. The deep-learning-based framework demonstrates significant potential to simultaneously accelerate imaging acquisition and enhance 3D reconstruction quality, offering further possibilities for computational microscopy.

Indexed as

Deep LearningImaging, Three-DimensionalMicroscopyAlgorithmsAnimalsFourier AnalysisMice3D reconstructiondeep learningFourier light-field microscopyhierarchical cascadeimage fusionlight-field microscopy

Identifiers

PMID41783388
PMCPMC12955040

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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.