TY - JOUR
T1 - Machine Learning Enabled Leukocyte Quantification Using Smartphone Coupled 3D Printed Microfluidic Biosensor
AU - Govindaraju, Harshitha
AU - Sami, Muhammad Ahsan
AU - Hassan, Umer
N1 - Funding Information:
This work was supported in part by the Department of Electrical and Computer Engineering, Global Health Institute at Rutgers, The State University of New Jersey, in part by the New Jersey Health Foundation, and in part by the National Science Foundation (NSF) under Award 2002511.
Publisher Copyright:
© 2013 IEEE.
PY - 2022
Y1 - 2022
N2 - Leukocyte quantification from whole blood can aid in detecting and managing infections, cardiovascular diseases, and immune system responses. In addition to traditional leukocyte quantification devices such as flow cytometers and benchtop fluorescent microscopes, smartphone-based particle quantifiers are becoming popular because they provide results at a fraction of the cost. One major limitation of these smartphone-based devices is their dependence on desktop computers for data processing, which keeps them from reaching their true translation potential as point of care (POC) devices. In this paper, we present a computer vision and machine learning-enabled methodology to count particles imaged from our 3D printed smartphone-coupled fluorescent microscope. Multiple convolution neural networks (CNN) using different filter sizes were implemented and trained with various learning rates (0.001, 0.0001) and batch sizes (8,16,32). The performance of these trained networks was then tested on green fluorescent microparticles and leukocytes and compared against the ground truth obtained using ImageJ. An R2 value of 0.99 was observed. Next, when cross-validation was done to validate the efficacy of the designed CNN architecture, and the predicted results showed a good correlation (R2 = 0.99) when compared against the ground truth. The performance of the trained model was also evaluated on particles conjugated with a different fluorophore and an R2 value of 0.99 was observed, showcasing its efficacy and versatility. This trained model was then integrated into an Application Programming Interface (API) and is available online for the broader community usage.
AB - Leukocyte quantification from whole blood can aid in detecting and managing infections, cardiovascular diseases, and immune system responses. In addition to traditional leukocyte quantification devices such as flow cytometers and benchtop fluorescent microscopes, smartphone-based particle quantifiers are becoming popular because they provide results at a fraction of the cost. One major limitation of these smartphone-based devices is their dependence on desktop computers for data processing, which keeps them from reaching their true translation potential as point of care (POC) devices. In this paper, we present a computer vision and machine learning-enabled methodology to count particles imaged from our 3D printed smartphone-coupled fluorescent microscope. Multiple convolution neural networks (CNN) using different filter sizes were implemented and trained with various learning rates (0.001, 0.0001) and batch sizes (8,16,32). The performance of these trained networks was then tested on green fluorescent microparticles and leukocytes and compared against the ground truth obtained using ImageJ. An R2 value of 0.99 was observed. Next, when cross-validation was done to validate the efficacy of the designed CNN architecture, and the predicted results showed a good correlation (R2 = 0.99) when compared against the ground truth. The performance of the trained model was also evaluated on particles conjugated with a different fluorophore and an R2 value of 0.99 was observed, showcasing its efficacy and versatility. This trained model was then integrated into an Application Programming Interface (API) and is available online for the broader community usage.
KW - Disease diagnostics
KW - Fluorescent microscopy
KW - Image processing
KW - Leukocyte counting
KW - Machine learning
KW - Point-of-care
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U2 - 10.1109/ACCESS.2022.3198692
DO - 10.1109/ACCESS.2022.3198692
M3 - Article
AN - SCOPUS:85137866315
SN - 2169-3536
VL - 10
SP - 85755
EP - 85763
JO - IEEE Access
JF - IEEE Access
ER -