Abstract

We present methods that automatically select a linear or nonlinear classifier for red blood cell (RBC) classification by analyzing the equality of the covariance matrices in Gabor-filtered holographic images. First, the phase images of the RBCs are numerically reconstructed from their holograms, which are recorded using off-axis digital holographic microscopy (DHM). Second, each RBC is segmented using a marker-controlled watershed transform algorithm and the inner part of the RBC is identified and analyzed. Third, the Gabor wavelet transform is applied to the segmented cells to extract a series of features, which then undergo a multivariate statistical test to evaluate the equality of the covariance matrices of the different shapes of the RBCs using selected features. When these covariance matrices are not equal, a nonlinear classification scheme based on quadratic functions is applied; otherwise, a linear classification is applied. We used the stomatocyte, discocyte, and echinocyte RBC for classifier training and testing. Simulation results demonstrated that 10 of the 14 RBC features are useful in RBC classification. Experimental results also revealed that the covariance matrices of the three main RBC groups are not equal and that a nonlinear classification method has a much lower misclassification rate. The proposed automated RBC classification method has the potential for use in drug testing and the diagnosis of RBC-related diseases.

Highlights

  • Red blood cells (RBCs) are essential components of human blood

  • The cells were incubated for 30 min at 37 °C before the chamber was mounted for off-axis digital holographic microscopy (DHM) imaging

  • We have proposed a statistical method for classifying RBCs based on 3D morphology and off-axis digital holographic microscopy

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Summary

Introduction

Red blood cells (RBCs) are essential components of human blood. They deliver oxygen to body tissues in vertebrates via the circulatory system, and absorb oxygen in the lungs and release it when flowing through the capillaries [1, 2]. The use of traditional 2D imaging systems for quantitative analysis of RBCs is limited because they cannot provide important biophysical cell parameters related to the structure and function of RBCs. development of an RBC classification method based on quantitative three-dimensional (3D) imaging with greater efficiency and accuracy is imperative. 3D imaging systems for the analysis of semitransparent or transparent biological specimens such as cardiomyocytes and RBCs have been presented [9,10,11,12,13,14,15,16,17,18,19,20,21]

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