TY - GEN
T1 - Realistic cross-domain microscopy via conditional generative adversarial networks
T2 - Medical Imaging 2020: Digital Pathology
AU - Nadarajan, Gouthamrajan
AU - Doyle, Scott
N1 - Publisher Copyright:
© 2020 SPIE. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Hematoxylin and Eosin (H&E) is a widely-used stain for diagnosis and prognosis in clinical pathology; it is a non-specific stain, binding to all cell types. Immunofluorescent (IF) staining is highly specific, binding only to targeted proteins in a sample to identify specific cellular and sub-cellular structures. IF images are costlier and more technically difficult compared with H&E, so are rarely used in routine clinical workup, but can be used for identification of diagnostically significant cell types. In previous work, we used registered IF and H&E images to generate class labels for training a deep learning H&E segmentation algorithm. In this work, we leverage this dataset to train a Conditional Generative Adversarial Network (cGAN) to generate realistic-looking H&E images from IF images stained for DAPI and ribosomal S6. Using these generated images, we trained a semantic segmentation algorithm to identify nuclei, cytoplasm, and membrane classes by thresholding the original IF stains for use as class labels on the generated H&E. The trained classifier was then used to segment a holdout dataset of real H&E images. We found that the semantic segmentation models trained on the generated H&E images (Dice score: 0.539) performed similarly to models trained on real H&E (Dice score: 0.503), suggesting that cGAN generated samples can be used as a viable training set for deep learning models that are intended to be applied on real H&E data.
AB - Hematoxylin and Eosin (H&E) is a widely-used stain for diagnosis and prognosis in clinical pathology; it is a non-specific stain, binding to all cell types. Immunofluorescent (IF) staining is highly specific, binding only to targeted proteins in a sample to identify specific cellular and sub-cellular structures. IF images are costlier and more technically difficult compared with H&E, so are rarely used in routine clinical workup, but can be used for identification of diagnostically significant cell types. In previous work, we used registered IF and H&E images to generate class labels for training a deep learning H&E segmentation algorithm. In this work, we leverage this dataset to train a Conditional Generative Adversarial Network (cGAN) to generate realistic-looking H&E images from IF images stained for DAPI and ribosomal S6. Using these generated images, we trained a semantic segmentation algorithm to identify nuclei, cytoplasm, and membrane classes by thresholding the original IF stains for use as class labels on the generated H&E. The trained classifier was then used to segment a holdout dataset of real H&E images. We found that the semantic segmentation models trained on the generated H&E images (Dice score: 0.539) performed similarly to models trained on real H&E (Dice score: 0.503), suggesting that cGAN generated samples can be used as a viable training set for deep learning models that are intended to be applied on real H&E data.
KW - Conditional Generative Adversarial Networks(cGAN)
KW - Hematoxylin and Eosin(H&E)
KW - Image to image translation
KW - Immunofluorescence
KW - Pix2pix
UR - https://www.scopus.com/pages/publications/85103249864
U2 - 10.1117/12.2549842
DO - 10.1117/12.2549842
M3 - Conference contribution
AN - SCOPUS:85103249864
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2020
A2 - Tomaszewski, John E.
A2 - Ward, Aaron D.
PB - SPIE
Y2 - 19 February 2020 through 20 February 2020
ER -