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Related Experiment Video

Updated: May 13, 2026

Acquiring Fluorescence Time-lapse Movies of Budding Yeast and Analyzing Single-cell Dynamics using GRAFTS
17:01

Acquiring Fluorescence Time-lapse Movies of Budding Yeast and Analyzing Single-cell Dynamics using GRAFTS

Published on: July 18, 2013

An algorithm to automate yeast segmentation and tracking.

Andreas Doncic1, Umut Eser, Oguzhan Atay

  • 1Department of Biology, Stanford University, Stanford, California, United States of America.

Plos One
|March 23, 2013
PubMed
Summary
This summary is machine-generated.

This study introduces an automated algorithm for segmenting and tracking budding yeast cells. The method uses yeast-specific traits for robust cell analysis, improving microscopy data interpretation.

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Area of Science:

  • Cellular biology
  • Microscopy techniques
  • Computational biology

Background:

  • Quantitative fluorescence microscopy advances cellular process understanding.
  • Single-cell imaging reveals phenomena like cell-to-cell variability, difficult to detect in population studies.
  • Accurate cell segmentation and tracking are crucial but challenging for analyzing dynamic cellular behaviors.

Purpose of the Study:

  • To develop a fully automated algorithm for segmenting and tracking budding yeast cells in colonies.
  • To overcome limitations in current cell segmentation and tracking methods.
  • To enable more robust analysis of dynamic cellular processes.

Main Methods:

  • Developed an algorithm for automated segmentation and tracking of budding yeast cells.
  • Incorporated yeast-specific traits (immobility, growth rate) into the segmentation process.
  • Utilized a set of threshold values, rather than a single optimized threshold, for robust image segmentation.

Main Results:

  • Achieved fully automated segmentation and tracking of budding yeast cells.
  • Demonstrated robust segmentation by using a range of threshold values.
  • The algorithm effectively handles the challenges of segmenting and tracking cells in growing colonies.

Conclusions:

  • The presented algorithm provides an efficient and robust solution for budding yeast cell segmentation and tracking.
  • This tool can significantly accelerate experimental pipelines relying on single-cell analysis.
  • Enhances the study of dynamic cellular processes and cell-to-cell variability.