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Related Concept Videos

Flow Cytometry01:23

Flow Cytometry

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The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
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Flow Cytometry Protocols for Surface and Intracellular Antigen Analyses of Neural Cell Types
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A computational streak mode cytometry biosensor for rare cell analysis.

Miguel Ossandon1, Joshua Balsam, Hugh Alan Bruck

  • 1National Cancer Institute, Rockville, MD 20850, USA. ossandom@mail.nih.gov.

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|January 31, 2017
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Summary
This summary is machine-generated.

A new computational biosensor enhances rare cell detection using streak mode imaging flow cytometry. This technology improves accuracy in identifying cells, even with low signal-to-noise ratios, for point-of-care testing applications.

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Area of Science:

  • Biomedical Engineering
  • Analytical Chemistry
  • Cell Biology

Background:

  • Streak mode imaging flow cytometry captures fluorescent cells as streaks, posing challenges for rare cell detection due to dynamic imaging conditions and low signal-to-noise ratios (SNR).
  • Existing methods struggle with enumerating rare cells, particularly when using low-resolution cameras suitable for point-of-care testing (POCT).

Purpose of the Study:

  • To develop and validate a novel computational biosensor approach for overcoming imaging challenges in rare cell detection.
  • To enhance the accuracy and efficiency of enumerating rare cells in large volumes using streak mode imaging.

Main Methods:

  • A computational biosensor was developed, integrating biosensing hardware with algorithms to analyze streak intensity, length, and location in consecutive frames.
  • Cell identification involved a three-part process: streak detection, candidate cell identification, and spurious cell filtering.
  • Experiments analyzed samples with 1 cell/mL at 10 mL/min flow rate, imaged at 4 frames per second.

Main Results:

  • The computational biosensor achieved 98% total cell detection (TD) compared to ground truth (GT) for images with SNR > 4.4 dB.
  • Detection accuracy decreased to 66% for low SNR images.
  • True positive cells detected (TP/GT) reached 91% for high SNR images.

Conclusions:

  • The computational biosensor demonstrates significant analytical capabilities for rare cell enumeration in large volumes, surpassing current technologies.
  • This approach offers a promising solution for accurate rare cell detection in POCT settings, addressing limitations of traditional imaging methods.