iCLOTS: open-source, artificial intelligence-enabled software for analyses of blood cells in microfluidic and microscopy-based assays.
Meredith E FayOluwamayokun OshinowoElizabeth IffrigKirby S FibbenChristina CarusoScott HansenJamie O MusickJosé M ValdezSally S AzerRobert G ManninoHyoann ChoiDan Y ZhangEvelyn K WilliamsErica N EvansCeleste K KanneMelissa L KempVivien A SheehanMarcus A CardenCarolyn M BennettDavid K WoodWilbur A LamPublished in: Nature communications (2023)
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.
Keyphrases
- high throughput
- cell adhesion
- machine learning
- artificial intelligence
- big data
- single cell
- deep learning
- rna seq
- single molecule
- data analysis
- induced apoptosis
- electronic health record
- cell cycle arrest
- label free
- pet imaging
- high resolution
- optical coherence tomography
- blood flow
- oxidative stress
- cell proliferation
- endoplasmic reticulum stress
- computed tomography