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Related Concept Videos

Yeast Signaling01:28

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Yeasts are single-celled organisms, but unlike bacteria, they are eukaryotes (cells with a nucleus). Cell signaling in yeast is similar to signaling in other eukaryotic cells. A ligand, such as a protein or a small molecule released from a yeast cell, attaches to a receptor on the cell surface. The binding stimulates second-messenger kinases to activate or inactivate transcription factors that further regulate gene expression. Many of the yeast intracellular signaling cascades have similar...
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Acquiring Fluorescence Time-lapse Movies of Budding Yeast and Analyzing Single-cell Dynamics using GRAFTS
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Morphologically constrained and data informed cell segmentation of budding yeast.

Elco Bakker1,2, Peter S Swain1,2, Matthew M Crane1,2

  • 1SynthSys-Synthetic and Systems Biology, University of Edinburgh, Edinburgh EH9 3BF, UK.

Bioinformatics (Oxford, England)
|October 3, 2017
PubMed
Summary
This summary is machine-generated.

Processing large datasets from time-lapse imaging is challenging, especially in microfluidic devices. DISCO (Data Informed Segmentation of Cell Objects) improves cell tracking and segmentation in microfluidics by using physical and temporal constraints.

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Area of Science:

  • Cell biology
  • Bioimage analysis
  • Microfluidics

Background:

  • High-content image cytometry generates vast datasets, posing challenges for time-lapse experiment analysis.
  • Existing automated single-cell segmentation methods struggle with microfluidic devices due to non-uniform fields of view and complex cell arrangements.
  • Poor segmentation performance in microfluidics hinders long-term cell imaging and analysis.

Purpose of the Study:

  • To develop a robust framework for cell tracking and segmentation in microfluidic devices.
  • To leverage physical and temporal constraints for improved image analysis.
  • To enhance the accuracy of automated cell segmentation in challenging imaging environments.

Main Methods:

  • Introduced DISCO (Data Informed Segmentation of Cell Objects), a novel framework for cell segmentation and tracking.
  • Integrated physical constraints of microfluidic traps, cell morphology, and temporal information (growth, motion).
  • Utilized manually curated datasets for training and validation.

Main Results:

  • DISCO demonstrated substantial improvements in both cell tracking and segmentation accuracy compared to existing software.
  • The framework effectively handles the complexities of cell behavior within microfluidic environments.
  • Performance gains were validated using curated ground-truth datasets.

Conclusions:

  • DISCO offers a significant advancement in analyzing time-lapse imaging data from microfluidic cell cultures.
  • The approach enhances the reliability of automated cell segmentation in non-ideal imaging conditions.
  • The developed framework facilitates more accurate and efficient long-term cell studies.