Nature Communications (Aug 2023)

iCLOTS: open-source, artificial intelligence-enabled software for analyses of blood cells in microfluidic and microscopy-based assays

  • Meredith E. Fay,
  • Oluwamayokun Oshinowo,
  • Elizabeth Iffrig,
  • Kirby S. Fibben,
  • Christina Caruso,
  • Scott Hansen,
  • Jamie O. Musick,
  • José M. Valdez,
  • Sally S. Azer,
  • Robert G. Mannino,
  • Hyoann Choi,
  • Dan Y. Zhang,
  • Evelyn K. Williams,
  • Erica N. Evans,
  • Celeste K. Kanne,
  • Melissa L. Kemp,
  • Vivien A. Sheehan,
  • Marcus A. Carden,
  • Carolyn M. Bennett,
  • David K. Wood,
  • Wilbur A. Lam

DOI
https://doi.org/10.1038/s41467-023-40522-4
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 16

Abstract

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Abstract While microscopy-based cellular assays, including microfluidics, have significantly advanced over the last several decades, there has not been concurrent development of widely-accessible techniques to analyze time-dependent microscopy data incorporating phenomena such as fluid flow and dynamic cell adhesion. As such, experimentalists typically rely on error-prone and time-consuming manual analysis, resulting in lost resolution and missed opportunities for innovative metrics. We present a user-adaptable toolkit packaged into the open-source, standalone Interactive Cellular assay Labeled Observation and Tracking Software (iCLOTS). We benchmark cell adhesion, single-cell tracking, velocity profile, and multiscale microfluidic-centric applications with blood samples, the prototypical biofluid specimen. Moreover, machine learning algorithms characterize previously imperceptible data groupings from numerical outputs. Free to download/use, iCLOTS addresses a need for a field stymied by a lack of analytical tools for innovative, physiologically-relevant assays of any design, democratizing use of well-validated algorithms for all end-user biomedical researchers who would benefit from advanced computational methods.