Evidence map›Paper›PMID 35588399›Full record

ArticlePloS one2022

High-throughput widefield fluorescence imaging of 3D samples using deep learning for 2D projection image restoration.

Edvin Forsgren, Christoffer Edlund, Miniver Oliver, Kalpana Barnes, Rickard Sjögren, Timothy R Jackson

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
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  5. Small Fish, Big Answers: Zebrafish and the Molecular Drivers of Metastasis.International journal of molecular sciences · 2025
    Review
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.

Edvin ForsgrenComputational Life Science Cluster (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.ORCID 0000-0002-1898-4453
Christoffer EdlundSartorius Corporate Research, Sartorius Stedim Data Analytics AB, Umeå, Sweden.
Miniver OliverSartorius BioAnalytics, Essen BioScience, Ltd., Units 2 & 3 The Quadrant, Royston, Hertfordshire, United Kingdom.
Kalpana BarnesSartorius BioAnalytics, Essen BioScience, Ltd., Units 2 & 3 The Quadrant, Royston, Hertfordshire, United Kingdom.
Rickard SjögrenSartorius Corporate Research, Sartorius Stedim Data Analytics AB, Umeå, Sweden.ORCID 0000-0001-7881-0968
Timothy R JacksonSartorius BioAnalytics, Essen BioScience, Ltd., Units 2 & 3 The Quadrant, Royston, Hertfordshire, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence microscopy is a core method for visualizing and quantifying the spatial and temporal dynamics of complex biological processes. While many fluorescent microscopy techniques exist, due to its cost-effectiveness and accessibility, widefield fluorescent imaging remains one of the most widely used. To accomplish imaging of 3D samples, conventional widefield fluorescence imaging entails acquiring a sequence of 2D images spaced along the z-dimension, typically called a z-stack. Oftentimes, the first step in an analysis pipeline is to project that 3D volume into a single 2D image because 3D image data can be cumbersome to manage and challenging to analyze and interpret. Furthermore, z-stack acquisition is often time-consuming, which consequently may induce photodamage to the biological sample; these are major barriers for workflows that require high-throughput, such as drug screening. As an alternative to z-stacks, axial sweep acquisition schemes have been proposed to circumvent these drawbacks and offer potential of 100-fold faster image acquisition for 3D-samples compared to z-stack acquisition. Unfortunately, these acquisition techniques generate low-quality 2D z-projected images that require restoration with unwieldy, computationally heavy algorithms before the images can be interrogated. We propose a novel workflow to combine axial z-sweep acquisition with deep learning-based image restoration, ultimately enabling high-throughput and high-quality imaging of complex 3D-samples using 2D projection images. To demonstrate the capabilities of our proposed workflow, we apply it to live-cell imaging of large 3D tumor spheroid cultures and find we can produce high-fidelity images appropriate for quantitative analysis. Therefore, we conclude that combining axial z-sweep image acquisition with deep learning-based image restoration enables high-throughput and high-quality fluorescence imaging of complex 3D biological samples.

Indexed as

Deep LearningAlgorithmsImage Processing, Computer-AssistedImaging, Three-DimensionalMicroscopy, FluorescenceOptical Imaging

Identifiers

PMID35588399
PMCPMC9119453

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LicenceCC BY
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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.