Sarc-Graph

Sarc-Graph performs automated segmentation, tracking, and quantitative analysis of z-discs and sarcomeres in fluorescently tagged human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) to characterize sarcomere architecture and dynamics.


Key Features:

  • Automated Segmentation: Segments z-discs and sarcomeres in fluorescently tagged hiPSC-CMs.
  • Tracking Capabilities: Tracks z-discs and sarcomeres in dynamically beating cells for temporal analysis.
  • Spatiotemporal Analysis and Visualization: Performs automated spatiotemporal analysis and generates visualizations of dynamic changes in cardiomyocytes.
  • Spatial Graph Construction: Constructs spatial graphs with z-discs as nodes and sarcomeres as edges to measure network distances between sarcomere pairs.
  • Deformation Gradient Computation: Computes an approximate deformation gradient across cell populations using tracked and segmented components as fiducial markers.

Scientific Applications:

  • Drug Discovery: Enables quantitative assessment of compound effects on sarcomere dynamics in hiPSC-CMs for screening applications.
  • Cardiac Repair Research: Provides measurements of sarcomere architecture and mechanical descriptors to study hiPSC-CM function relevant to cardiac repair.

Methodology:

Processes synthetic and experimental movies of beating hiPSC-CMs, performs automated segmentation of z-discs and sarcomeres, tracks these components over time, constructs spatial graphs (z-discs as nodes, sarcomeres as edges), and computes approximate deformation gradients using tracked/segmented components as fiducial markers.

Topics

Details

License:
MIT
Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python
Added:
3/29/2022
Last Updated:
3/29/2022

Operations

Publications

Zhao B, Zhang K, Chen CS, Lejeune E. Sarc-Graph: Automated segmentation, tracking, and analysis of sarcomeres in hiPSC-derived cardiomyocytes. PLOS Computational Biology. 2021;17(10):e1009443. doi:10.1371/journal.pcbi.1009443. PMID:34613960. PMCID:PMC8523047.

PMID: 34613960
PMCID: PMC8523047
Funding: - CELL-MET Engineering Research Center National Science Foundation: ECC-1647837 - American Heart Association: 17PRE33660967