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Microscopy Research and TechniqueVolume 87, Issue 8, August 2024, Pages 1718-1732

Automated segmentation of cell organelles in volume electron microscopy using deep learning(Article)(Open Access)

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  • aDepartment of Computer Science and Electrical Engineering, Singidunum University, Belgrade, Serbia
  • bCryoCapCell, Le Kremlin-Bicêtre, France
  • cAustrian BioImaging, Vienna BioCenter Core Facilities, Vienna, Austria
  • dLudwig Boltzmann Institute for Experimental and Clinical Traumatology in the AUVA Trauma Research Center, Vienna, Austria
  • eDepartment for Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, Sweden
  • fCentre for Optical Technologies, Aalen University, Aalen, Germany
  • gDepartment of Computer Science, Dalian University of Technology, Dalian, China
  • hDepartment of Computer Science, Dalian Maritime University, Dalian, China
  • iFaculty of Computer Information, Higher Colleges of Technology, Abu Dhabi, United Arab Emirates
  • jElectron Microscopy STP, The Francis Crick Institute, London, United Kingdom

Abstract

Recent advances in computing power triggered the use of artificial intelligence in image analysis in life sciences. To train these algorithms, a large enough set of certified labeled data is required. The trained neural network is then capable of producing accurate instance segmentation results that will then need to be re-assembled into the original dataset: the entire process requires substantial expertise and time to achieve quantifiable results. To speed-up the process, from cell organelle detection to quantification across electron microscopy modalities, we propose a deep-learning based approach for fast automatic outline segmentation (FAMOUS), that involves organelle detection combined with image morphology, and 3D meshing to automatically segment, visualize and quantify cell organelles within volume electron microscopy datasets. From start to finish, FAMOUS provides full segmentation results within a week on previously unseen datasets. FAMOUS was showcased on a HeLa cell dataset acquired using a focused ion beam scanning electron microscope, and on yeast cells acquired by transmission electron tomography. Research Highlights: Introducing a rapid, multimodal machine-learning workflow for the automatic segmentation of 3D cell organelles. Successfully applied to a variety of volume electron microscopy datasets and cell lines. Outperforming manual segmentation methods in time and accuracy. Enabling high-throughput quantitative cell biology. © 2024 The Authors. Microscopy Research and Technique published by Wiley Periodicals LLC.

Author keywords

automated segmentationcell biologyimage analysisneural-networkvolume electron microscopy

Indexed keywords

Engineering controlled terms:Cell cultureCellsDeep learningElectric impedance tomographyElectron microscopesElectronsHigh resolution transmission electron microscopyImage segmentationIon beamsMedical imagingScanning electron microscopyStrontium titanates
Engineering uncontrolled termsAutomated segmentationCell biologyCell organelleComputing powerImage-analysisLife-sciencesNeural-networksSegmentation resultsVolume electron microscopyVolume electrons
Engineering main heading:Image analysis
EMTREE medical terms:algorithmartificial neural networkcell organellecytologydeep learningelectron microscopyHeLa cell linehumanimage processingproceduresSaccharomyces cerevisiaethree-dimensional imagingultrastructurevolume electron microscopy
MeSH:AlgorithmsDeep LearningHeLa CellsHumansImage Processing, Computer-AssistedImaging, Three-DimensionalMicroscopy, ElectronNeural Networks, ComputerOrganellesSaccharomyces cerevisiaeVolume Electron Microscopy

Funding details

Funding sponsor Funding number Acronym
Medical Research Council
See opportunities by MRC
MRC
Francis Crick Institute
See opportunities by FCI
FCI
Wellcome Trust
See opportunities by WT
WT
European Cooperation in Science and TechnologyCA17121COST
European Cooperation in Science and TechnologyCOST
Cancer Research UK
See opportunities by CRUK
CC1076CRUK
Cancer Research UK
See opportunities by CRUK
CRUK
Knut och Alice Wallenbergs Stiftelse2017.0091
Knut och Alice Wallenbergs Stiftelse
Vetenskapsrådet2019‐04004VR
VetenskapsrådetVR
  • 1

    This article is based upon work from COST Action CA17121, supported by COST (European Cooperation in Science and Technology): www.comulis.eu (Walter, Kleywegt, & Verkade, 2021 ). We thank the Electron Microscopy STP at the Francis Crick Institute. The work of Christopher J. Peddie was supported by the Francis Crick Institute, which receives its core funding from Cancer Research UK (CC1076), the UK Medical Research Council (CC1076), and the Wellcome Trust (CC1076). This work was supported by a grant from Knut och Alice Wallenbergs Stiftelse (2017.0091) and Swedish Research Council grant 2019‐04004 to Johanna L. Höög. Open Access funding enabled and organized by Projekt DEAL.

  • ISSN: 1059910X
  • CODEN: MRTEE
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1002/jemt.24548
  • PubMed ID: 38501891
  • Document Type: Article
  • Publisher: John Wiley and Sons Inc

  Stojmenović, M.; Department of Computer Science and Electrical Engineering, Singidunum University, Belgrade, Serbia;
  Walter, A.; Aalen University of Applied Sciences, Aalen, Germany;
© Copyright 2024 Elsevier B.V., All rights reserved.

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