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Tutorials:

  • Get started
  • Your First Experiment
  • A Two-Population Experiment
  • Processing an experiment with the API

How-to guides

  • How-to guides
    • Basics
      • How to create a new experiment
      • How to register stacks with Fiji
      • How to correct a fluorescent background
      • How to perform a model-free background correction
      • How to align two channels
      • How to segment with the Threshold Configuration Wizard
      • How to apply a segmentation model
      • How to annotate a group of cells
      • How to annotate an event
      • How to annotate a dataset for segmentation
      • How to configure and run tracking
      • How to correct a single-cell track
      • How to perform conditional cell classification
      • How to detect sub-cellular spots
      • How to measure locally corrected intensities
      • How to measure edge intensity
      • How to measure single-cell texture
      • How to measure cell-cell interactions
      • How to visualize cell-cell interactions
      • How to compare collapsed measurements across conditions
      • How to detect an event using conditions
      • How to plot survival between two events
      • How to synchronize single-cell timeseries over a population
    • Advanced
  • Troubleshooting

Reference:

  • Installation Reference
  • Settings & Parameters
  • Supported File Formats
  • UI Menus & Shortcuts
  • Measurements Reference
  • Glossary
  • API

Explanation:

  • Topic Overviews
  • Concepts

About:

  • Acknowledegments
  • How to cite?
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  • How-to guides
  • Basics
  • View page source

Basics

  • How to create a new experiment
  • How to register stacks with Fiji
  • How to correct a fluorescent background
  • How to perform a model-free background correction
  • How to align two channels
  • How to segment with the Threshold Configuration Wizard
  • How to apply a segmentation model
  • How to annotate a group of cells
  • How to annotate an event
  • How to annotate a dataset for segmentation
  • How to configure and run tracking
  • How to correct a single-cell track
  • How to perform conditional cell classification
  • How to detect sub-cellular spots
  • How to measure locally corrected intensities
  • How to measure edge intensity
  • How to measure single-cell texture
  • How to measure cell-cell interactions
  • How to visualize cell-cell interactions
  • How to compare collapsed measurements across conditions
  • How to detect an event using conditions
  • How to plot survival between two events
  • How to synchronize single-cell timeseries over a population
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