The development of an automated microscope image tracking and analysis system

Author:

McAfee Lillian1,Heath Zach2,Anderson William1,Hozi Marvin2,Orr John Walker2,Kang Youngbok (Abraham)1ORCID

Affiliation:

1. Department of Mechanical, Civil, and Biomedical Engineering George Fox University Newberg Oregon USA

2. Department of Computer science George Fox University Newberg Oregon USA

Abstract

AbstractMicroscopy image analysis plays a crucial role in understanding cellular behavior and uncovering important insights in various biological and medical research domains. Tracking cells within the time‐lapse microscopy images is a fundamental technique that enables the study of cell dynamics, interactions, and migration. While manual cell tracking is possible, it is time‐consuming and prone to subjective biases that impact results. In order to solve this issue, we sought to create an automated software solution, named cell analyzer, which is able to track cells within microscopy images with minimal input required from the user. The program of cell analyzer was written in Python utilizing the open source computer vision (OpenCV) library and featured a graphical user interface that makes it easy for users to access. The functions of all codes were verified through closeness, area, centroid, contrast, variance, and cell tracking test. Cell analyzer primarily utilizes image preprocessing and edge detection techniques to isolate cell boundaries for detection and analysis. It uniquely recorded the area, displacement, speed, size, and direction of detected cell objects and visualized the data collected automatically for fast analysis. Our cell analyzer provides an easy‐to‐use tool through a graphical user interface for tracking cell motion and analyzing quantitative cell images.

Funder

George Fox University

Publisher

Wiley

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