Evidence map›Paper›PMID 38903737›Full record

ArticleArXiv2024

Convolutional Neural Network Transformer (CNNT) for Fluorescence Microscopy image Denoising with Improved Generalization and Fast Adaptation.

Azaan Rehman, Alexander Zhovmer, Ryo Sato, Yosuke Mukoyama, Jiji Chen, Alberto Rissone, Rosa Puertollano, Harshad Vishwasrao, Hari Shroff, Christian A Combs and 1 more

Abstract readPreprint
In one paragraph

Article in ArXiv, 2024. 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

5 · Who and what money

Authors and funding

11 authors.

Azaan RehmanOffice of AI Research, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
Alexander ZhovmerCenter for Biologics Evaluation and Research, U.S. Food and Drug Administration (FDA), Silver Spring, Maryland 20903, United States.
Ryo SatoLaboratory of Stem Cell and Neurovascular Research, NHLBI, NIH, Bethesda, MD 20892, USA.
Yosuke MukoyamaLaboratory of Stem Cell and Neurovascular Research, NHLBI, NIH, Bethesda, MD 20892, USA.
Jiji ChenAdvanced Imaging and Microscopy Resource, NIBIB, NIH, Bethesda, MD 20892, USA.
Alberto RissoneLaboratory of Protein Trafficking and Organelle Biology, NHLBI, NIH, Bethesda, MD 20892, USA.
Rosa PuertollanoLaboratory of Protein Trafficking and Organelle Biology, NHLBI, NIH, Bethesda, MD 20892, USA.
Harshad VishwasraoAdvanced Imaging and Microscopy Resource, NIBIB, NIH, Bethesda, MD 20892, USA.
Hari ShroffJanelia Research Campus, Howard Hughes Medical Institute (HHMI), Ashburn, VA, USA.
Christian A CombsLight Microscopy Core, NHLBI, NIH, Bethesda, MD 20892, USA.
Hui XueOffice of AI Research, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Funding

Role of endolysosomal channels in calcium homeostasis and traffickingZIAHL006075 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI PUERTOLLANO, ROSA · 2010 to 2025
$8.7M
6 · The paper itself

Abstract

Deep neural networks have been applied to improve the image quality of fluorescence microscopy imaging. Previous methods are based on convolutional neural networks (CNNs) which generally require more time-consuming training of separate models for each new imaging experiment, impairing the applicability and generalization. Once the model is trained (typically with tens to hundreds of image pairs) it can then be used to enhance new images that are like the training data. In this study, we proposed a novel imaging-transformer based model, Convolutional Neural Network Transformer (CNNT), to outperform the CNN networks for image denoising. In our scheme we have trained a single CNNT based "backbone model" from pairwise high-low SNR images for one type of fluorescence microscope (instance structured illumination, iSim). Fast adaption to new applications was achieved by fine-tuning the backbone on only 5-10 sample pairs per new experiment. Results show the CNNT backbone and fine-tuning scheme significantly reduces the training time and improves the image quality, outperformed training separate models using CNN approaches such as - RCAN and Noise2Fast. Here we show three examples of the efficacy of this approach on denoising wide-field, two-photon and confocal fluorescence data. In the confocal experiment, which is a 5×5 tiled acquisition, the fine-tuned CNNT model reduces the scan time form one hour to eight minutes, with improved quality.

Identifiers

PMID38903737
PMCPMC11188127

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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.