TY - GEN
T1 - Conditional generative adversarial networks for H&E to if domain transfer
T2 - Medical Imaging 2021: Digital Pathology
AU - Nadarajan, Gouthamrajan
AU - Doyle, Scott
N1 - Publisher Copyright:
© COPYRIGHT SPIE. Downloading of the abstract is permitted for personal use only.
PY - 2021
Y1 - 2021
N2 - In this work, we explore image-to-image translation using Conditional Generative Adversarial Networks (cGAN) to convert digital tissue images from the brightfield to the immunofluorescence (IF) domain. A dataset of 149 tissue microarray (TMA) cores were stained using a multiplexed IF system for DAPI, Ribosomal S6, and NaKATPase. These TMA cores were subsequently stained with hematoxylin and eosin (H&E) and digitally scanned. Using registered pairs of H&E and IF, a cGAN was trained to translate from the H&E to the IF domain for DAPI, Ribosomal S6, and NaKATPase markers. This classifier was then evaluated by translating a set of holdout H&E samples, both from the original TMA dataset as well as an independent prostate cancer H&E dataset (for which we do not have IF probes). The cGAN was evaluated quantitatively for our multiplexed TMA samples and qualitatively for the independent H&E dataset. We found that for the DAPI channel, the cGAN is able to produce accurate samples but is unable to replicate the subtle pixel intensity differences that characterize boundaries between nuclei. For the NaKATPase and Ribosomal S6 channels, the cGAN over segmented extracellular matrix regions. On the holdout open-source H&E stained prostate tissue dataset, the cGAN produced qualitatively acceptable results.
AB - In this work, we explore image-to-image translation using Conditional Generative Adversarial Networks (cGAN) to convert digital tissue images from the brightfield to the immunofluorescence (IF) domain. A dataset of 149 tissue microarray (TMA) cores were stained using a multiplexed IF system for DAPI, Ribosomal S6, and NaKATPase. These TMA cores were subsequently stained with hematoxylin and eosin (H&E) and digitally scanned. Using registered pairs of H&E and IF, a cGAN was trained to translate from the H&E to the IF domain for DAPI, Ribosomal S6, and NaKATPase markers. This classifier was then evaluated by translating a set of holdout H&E samples, both from the original TMA dataset as well as an independent prostate cancer H&E dataset (for which we do not have IF probes). The cGAN was evaluated quantitatively for our multiplexed TMA samples and qualitatively for the independent H&E dataset. We found that for the DAPI channel, the cGAN is able to produce accurate samples but is unable to replicate the subtle pixel intensity differences that characterize boundaries between nuclei. For the NaKATPase and Ribosomal S6 channels, the cGAN over segmented extracellular matrix regions. On the holdout open-source H&E stained prostate tissue dataset, the cGAN produced qualitatively acceptable results.
UR - https://www.scopus.com/pages/publications/85103270710
U2 - 10.1117/12.2581098
DO - 10.1117/12.2581098
M3 - Conference contribution
AN - SCOPUS:85103270710
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2021
A2 - Tomaszewski, John E.
A2 - Ward, Aaron D.
PB - SPIE
Y2 - 15 February 2021 through 19 February 2021
ER -