Related Experiment Video
Updated: Jul 9, 2026

12:41
Multiparametric Tumor Organoid Drug Screening Using Widefield Live-Cell Imaging for Bulk and Single-Organoid Analysis
Published on: December 23, 2022
The large-scale digital cell analysis system: an open system for nonperturbing live cell imaging
Paul J Davis1, Elizabeth A Kosmacek, Yuansheng Sun
1Department of Biomedical Engineering, University of Iowa, Iowa City, IA, USA.
Journal of Microscopy
|November 30, 2007
Summary
The Large-Scale Digital Cell Analysis System (LSDCAS) enables live cell imaging with minimal cell growth perturbation. While phase-contrast microscopy is non-disruptive, fluorescence imaging with LSDCAS shows measurable growth changes in tested cell lines.
Area of Science:
- * Live cell imaging and analysis
- * Computational biology and bioinformatics
- * Microscopy techniques
Background:
- * Development of advanced live cell imaging systems is crucial for biological research.
- * Existing systems may introduce perturbations affecting cell behavior and experimental outcomes.
- * Need for open-source, extensible platforms for reproducible cell analysis.
Purpose of the Study:
- * To introduce the Large-Scale Digital Cell Analysis System (LSDCAS) as an open-source live cell imaging solution.
- * To evaluate the impact of LSDCAS imaging on cell growth kinetics and viability.
- * To compare the effects of phase-contrast and fluorescence microscopy on cell behavior within the LSDCAS framework.
Main Methods:
- * Design and implementation of a modular software system for data acquisition, management, and analysis.
- * Utilization of GNU/Linux operating system for LSDCAS software.
- * Comparative analysis of cell growth data from LSDCAS-imaged cells versus cells in CO(2) incubators.
Main Results:
- * LSDCAS demonstrated minimal perturbation on cell growth when using phase-contrast imaging.
- * Fluorescence image acquisition using LSDCAS resulted in measurable growth perturbation in the tested cell lines.
- * Cell growth data showed no significant difference between LSDCAS-imaged cells and control cells for phase-contrast microscopy.
Conclusions:
- * LSDCAS provides a non-perturbing platform for live cell imaging, particularly with phase-contrast microscopy.
- * Fluorescence imaging within LSDCAS can induce measurable changes in cell growth kinetics, necessitating careful consideration.
- * The open-source nature and graphical interface of LSDCAS facilitate its adoption in research settings.

