Evaluation of tile artifact correction methods for multiphoton microscopy mosaics of whole-slide tissue sections
Affiliation
Department of Biomedical Engineering, University of ArizonaWyant College of Optical Sciences, University of Arizona
College of Medicine, University of Arizona
Issue Date
2022
Metadata
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SPIECitation
Knapp, T., Lima, N., Duan, S., Merchant, J. L., & Sawyer, T. W. (2022). Evaluation of tile artifact correction methods for multiphoton microscopy mosaics of whole-slide tissue sections. Progress in Biomedical Optics and Imaging - Proceedings of SPIE, 11966.Rights
Copyright © 2022 SPIE.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Multi-photon microscopy (MPM) is a useful biomedical imaging tool due, in part, to its capabilities of probing tissue biomarkers at high resolution and with depth-resolved capabilities. Automated MPM tile scanning allows for whole-slide image acquisition but suffers from tile-stitching artifacts that prevent accurate quantitative data analysis. We have investigated a variety of post-processing artifact correction methods using ImageJ macros and custom Python/ MATLAB code and present a quantitative and qualitative comparison of these methods using whole-slide MPM autofluorescence images of human duodenal tissue. Image quality is assessed via evaluation of artifact removal compared to the calculated mean square error (MSE), peak signal-to-noise ratio (PSNR), and structural similarity index (SSIM) of the processed image and its raw counterpart. Consideration of both quantitative and qualitative results suggest a combination of flat-field based correction and frequency filtering processing steps provide improved artifact correction when compared to each method used independently to correct for tiling artifacts of tile-scan MPM images. © 2022 SPIE.Note
Immediate accessISSN
1605-7422ISBN
9781510648036Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1117/12.2609634
