TY - GEN
T1 - Automated multi-class ground-truth labeling of H&E images for deep learning using multiplexed fluorescence microscopy
AU - Nadarajan, Gouthamrajan
AU - Hope, Tyna
AU - Wang, Dan
AU - Cheung, Alison
AU - Ginty, Fiona
AU - Yaffe, Martin J.
AU - Doyle, Scott
N1 - Publisher Copyright:
© 2019 SPIE.
PY - 2019
Y1 - 2019
N2 - Manual annotation of Hematoxylin and Eosin (H&E) stained tissue images for deep learning classification is difficult, time consuming, and error-prone particularly for multi-class and rare-class problems. Chemical probes in immunohistochemistry (IHC) or immunofluorescence (IF) can automatically tag cellular structures; however, chemical labeling is difficult to use in training a deep classifier for H&E images (e.g. through serial sectioning and registration). In this work, we leverage the novel Multiplexed Immuno-Fluorescencent (MxIF) microscopy method developed by General Electric Global Research Center (GE GRC) which allows sequential, stain-image-bleach (SSB) application of protein markers on formalin-fixed, paraffin-embedded(FFPE) samples followed by traditional H&E staining to build chemically-annotated tissue maps of nuclei, cytoplasm, and cell membranes. This allows us to automate the creation of ground truth class-label maps for training an H&E-based tissue classifier. In this study, a tissue microarray consisting of 149 breast cancer and normal tissue cores were stained using MxIF for our three analytes, followed by traditional H&E staining. The MxIF stains for each TMA core were combined to create a "Virtual H&E" image, which is registered with the corresponding real H&E images. Each MxIF stained spot was segmented to obtain a class-label map for each analyte, which was then applied to the real H&E image to build a dataset consisting of the three analytes. A convolutional neural network (CNN) was then trained to classify this dataset. This system achieved an overall accuracy of 70%, suggesting that the MxIF system can provide useful labels for identifying hard to distinguish structures. A U-net was also trained to generate pseudo-IF stains from H&E and resulted in similar results.
AB - Manual annotation of Hematoxylin and Eosin (H&E) stained tissue images for deep learning classification is difficult, time consuming, and error-prone particularly for multi-class and rare-class problems. Chemical probes in immunohistochemistry (IHC) or immunofluorescence (IF) can automatically tag cellular structures; however, chemical labeling is difficult to use in training a deep classifier for H&E images (e.g. through serial sectioning and registration). In this work, we leverage the novel Multiplexed Immuno-Fluorescencent (MxIF) microscopy method developed by General Electric Global Research Center (GE GRC) which allows sequential, stain-image-bleach (SSB) application of protein markers on formalin-fixed, paraffin-embedded(FFPE) samples followed by traditional H&E staining to build chemically-annotated tissue maps of nuclei, cytoplasm, and cell membranes. This allows us to automate the creation of ground truth class-label maps for training an H&E-based tissue classifier. In this study, a tissue microarray consisting of 149 breast cancer and normal tissue cores were stained using MxIF for our three analytes, followed by traditional H&E staining. The MxIF stains for each TMA core were combined to create a "Virtual H&E" image, which is registered with the corresponding real H&E images. Each MxIF stained spot was segmented to obtain a class-label map for each analyte, which was then applied to the real H&E image to build a dataset consisting of the three analytes. A convolutional neural network (CNN) was then trained to classify this dataset. This system achieved an overall accuracy of 70%, suggesting that the MxIF system can provide useful labels for identifying hard to distinguish structures. A U-net was also trained to generate pseudo-IF stains from H&E and resulted in similar results.
KW - H & E
KW - Immunofluorescence
KW - Multiplexed Immuno-Fluorescencent (MxIF) microscopy
KW - Multiplexing
KW - Segmentation
KW - Unet
UR - https://www.scopus.com/pages/publications/85068661697
U2 - 10.1117/12.2512991
DO - 10.1117/12.2512991
M3 - Conference contribution
AN - SCOPUS:85068661697
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2019
A2 - Tomaszewski, John E.
A2 - Ward, Aaron D.
PB - SPIE
T2 - Medical Imaging 2019: Digital Pathology
Y2 - 20 February 2019 through 21 February 2019
ER -