Evidence map›Paper›PMID 36469001›Full record

ArticleThe Journal of cell biology2023

Deep neural network automated segmentation of cellular structures in volume electron microscopy.

Benjamin Gallusser, Giorgio Maltese, Giuseppe Di Caprio, Tegy John Vadakkan, Anwesha Sanyal, Elliott Somerville, Mihir Sahasrabudhe, Justin O'Connor, Martin Weigert, Tom Kirchhausen

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.0field-weighted citation impact, top 4% of its field
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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Presynaptic Vesicles Supply Membrane for Axonal Bouton Enlargement during Long Term Potentiation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  7. CabioRxiv : the preprint server for biology · 2026
    Article
  8. Leveraging AI for cell biology discovery.Biochemical Society transactions · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Segment Anything for Microscopy.Nature methods · 2025
    Article
  16. Article
  17. Review
  18. Electron Microscopy Techniques for 3D Plant ER Imaging.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Benjamin Gallusser *Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.ORCID 0000-0002-7906-4714
Giorgio Maltese *Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.ORCID 0000-0001-5252-4330
Giuseppe Di Caprio *Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.ORCID 0000-0001-5564-8064
Tegy John VadakkanProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.
Anwesha SanyalProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.ORCID 0000-0002-1456-8604
Elliott SomervilleProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.
Mihir SahasrabudheProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.ORCID 0000-0001-5993-3436
Justin O'ConnorDepartment of Biological Chemistry & Molecular Pharmacology, Harvard Medical School, Boston, MA.ORCID 0000-0002-4542-2472
Martin WeigertInstitute of Bioengineering, School of Life Sciences, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.ORCID 0000-0002-7780-9057
Tom KirchhausenProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA.ORCID 0000-0003-0559-893X
Boston Children's Hospital · USÉcole Polytechnique Fédérale de Lausanne · CHHarvard University · US

Funding

VISUALIZATION OF SUBCELLULAR DYNAMICS IN MULTICELLULAR ORGANISMSR35GM130386 · NIGMS · BOSTON CHILDREN'S HOSPITAL · PI TOMAS KIRCHHAUSEN · 2019 to 2026
$4.0M
NIGMS NIH HHS R35 GM130386
6 · The paper itself

Abstract

Volume electron microscopy is an important imaging modality in contemporary cell biology. Identification of intracellular structures is a laborious process limiting the effective use of this potentially powerful tool. We resolved this bottleneck with automated segmentation of intracellular substructures in electron microscopy (ASEM), a new pipeline to train a convolutional neural network to detect structures of a wide range in size and complexity. We obtained dedicated models for each structure based on a small number of sparsely annotated ground truth images from only one or two cells. Model generalization was improved with a rapid, computationally effective strategy to refine a trained model by including a few additional annotations. We identified mitochondria, Golgi apparatus, endoplasmic reticulum, nuclear pore complexes, caveolae, clathrin-coated pits, and vesicles imaged by focused ion beam scanning electron microscopy. We uncovered a wide range of membrane-nuclear pore diameters within a single cell and derived morphological metrics from clathrin-coated pits and vesicles, consistent with the classical constant-growth assembly model.

Indexed as

Image Processing, Computer-AssistedMicroscopy, ElectronNeural Networks, ComputerCaveolaeCell BiologyClathrinEndoplasmic ReticulumGolgi ApparatusMitochondriaNuclear PoreClathrin

Identifiers

PMID36469001
PMCPMC9728137
OpenAlexW4310943042

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.