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Updated: Jul 24, 2025

Author Spotlight: Advancements in Correlative Light and Electron Microscopy with Fluorescent Protein Preservation
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DeepCLEM: automated registration for correlative light and electron microscopy using deep learning.

Rick Seifert1,2, Sebastian M Markert2, Sebastian Britz2

  • 1Center for Computational and Theoretical Biology, University of Würzburg, Würzburg, 97074, Germany.

F1000Research
|July 3, 2023
PubMed
Summary
This summary is machine-generated.

DeepCLEM automates correlative light and electron microscopy (CLEM) registration by predicting fluorescence from EM images. This novel approach eliminates manual alignment, improving precision for biological imaging workflows.

Keywords:
Correlative MicroscopyDeep LearningImage RegistrationIn-silico labeling

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Area of Science:

  • Microscopy
  • Biotechnology
  • Computational Biology

Background:

  • Correlative Light and Electron Microscopy (CLEM) requires precise image registration between fluorescence and electron microscopy (EM) datasets.
  • Current registration methods are often manual or semi-automated, relying on fluorescent stains or fiducial markers, which can be time-consuming and introduce inaccuracies.
  • Differences in image contrast between fluorescence and EM modalities hinder direct automated alignment.

Purpose of the Study:

  • To develop a fully automated workflow for precise image registration in CLEM.
  • To overcome the limitations of manual and semi-automated registration methods in CLEM.
  • To provide a robust and adaptable solution for correlating imaging data.

Main Methods:

  • Introduction of DeepCLEM, a novel, fully automated workflow for CLEM registration.
  • Utilizing a convolutional neural network (CNN) to predict fluorescent signals directly from EM images.
  • Employing correlation-based alignment to register the predicted fluorescent signal with the experimentally measured chromatin signal.

Main Results:

  • DeepCLEM achieves fully automated registration of fluorescent and EM images.
  • The workflow accurately predicts fluorescent signals from EM data.
  • Successful registration is demonstrated using correlation-based alignment with chromatin signals.

Conclusions:

  • DeepCLEM offers a significant advancement in automating CLEM image registration.
  • The Fiji plugin facilitates accessibility and integration into existing microscopy workflows.
  • The methodology holds potential for adaptation to other imaging modalities and 3D datasets.