Evidence map›Paper›PMID 38505631›Full record

ArticleBiophysics reviews2021

Extracting quantitative biological information from bright-field cell images using deep learning.

Saga Helgadottir, Benjamin Midtvedt, Jesús Pineda, Alan Sabirsh, Caroline B Adiels, Stefano Romeo, Daniel Midtvedt, Giovanni Volpe

Abstract read
In one paragraph

Article in Biophysics reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Deep Learning-Powered Scalable Cancer Organ Chip for Cancer Precision Medicine.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Article
  5. Leveraging AI for cell biology discovery.Biochemical Society transactions · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Deep learning in light-matter interactions.Nanophotonics (Berlin, Germany) · 2022
    Review
  14. 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

8 authors.

Saga HelgadottirDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0001-8070-147X
Benjamin MidtvedtDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0001-9386-4753
Jesús PinedaDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0002-9197-3451
Alan SabirshAdvanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca, Gothenburg, Sweden.ORCID https://orcid.org/0000-0001-5310-0281
Caroline B AdielsDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0002-2403-2213
Stefano Romeo
Daniel MidtvedtDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.
Giovanni VolpeDepartment of Physics, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0001-5057-1846

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative analysis of cell structures is essential for biomedical and pharmaceutical research. The standard imaging approach relies on fluorescence microscopy, where cell structures of interest are labeled by chemical staining techniques. However, these techniques are often invasive and sometimes even toxic to the cells, in addition to being time consuming, labor intensive, and expensive. Here, we introduce an alternative deep-learning-powered approach based on the analysis of bright-field images by a conditional generative adversarial neural network (cGAN). We show that this is a robust and fast-converging approach to generate virtually stained images from the bright-field images and, in subsequent downstream analyses, to quantify the properties of cell structures. Specifically, we train a cGAN to virtually stain lipid droplets, cytoplasm, and nuclei using bright-field images of human stem-cell-derived fat cells (adipocytes), which are of particular interest for nanomedicine and vaccine development. Subsequently, we use these virtually stained images to extract quantitative measures about these cell structures. Generating virtually stained fluorescence images is less invasive, less expensive, and more reproducible than standard chemical staining; furthermore, it frees up the fluorescence microscopy channels for other analytical probes, thus increasing the amount of information that can be extracted from each cell. To make this deep-learning-powered approach readily available for other users, we provide a Python software package, which can be easily personalized and optimized for specific virtual-staining and cell-profiling applications.

Identifiers

PMID38505631
PMCPMC10903417

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Registered trials

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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.