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HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning

Deep learning has been effective for histology image analysis in digital pathology. However, many current deep learning approaches require large, strongly- or weakly labeled images and regions of interest, which can be time-consuming and resource-intensive to obtain. To address this challenge, we pr...

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Detalles Bibliográficos
Autores principales: DiPalma, Joseph, Torresani, Lorenzo, Hassanpour, Saeed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339175/
https://www.ncbi.nlm.nih.gov/pubmed/37457594
http://dx.doi.org/10.1016/j.jpi.2023.100320
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author DiPalma, Joseph
Torresani, Lorenzo
Hassanpour, Saeed
author_facet DiPalma, Joseph
Torresani, Lorenzo
Hassanpour, Saeed
author_sort DiPalma, Joseph
collection PubMed
description Deep learning has been effective for histology image analysis in digital pathology. However, many current deep learning approaches require large, strongly- or weakly labeled images and regions of interest, which can be time-consuming and resource-intensive to obtain. To address this challenge, we present HistoPerm, a view generation method for representation learning using joint embedding architectures that enhances representation learning for histology images. HistoPerm permutes augmented views of patches extracted from whole-slide histology images to improve classification performance. We evaluated the effectiveness of HistoPerm on 2 histology image datasets for Celiac disease and Renal Cell Carcinoma, using 3 widely used joint embedding architecture-based representation learning methods: BYOL, SimCLR, and VICReg. Our results show that HistoPerm consistently improves patch- and slide-level classification performance in terms of accuracy, F1-score, and AUC. Specifically, for patch-level classification accuracy on the Celiac disease dataset, HistoPerm boosts BYOL and VICReg by 8% and SimCLR by 3%. On the Renal Cell Carcinoma dataset, patch-level classification accuracy is increased by 2% for BYOL and VICReg, and by 1% for SimCLR. In addition, on the Celiac disease dataset, models with HistoPerm outperform the fully supervised baseline model by 6%, 5%, and 2% for BYOL, SimCLR, and VICReg, respectively. For the Renal Cell Carcinoma dataset, HistoPerm lowers the classification accuracy gap for the models up to 10% relative to the fully supervised baseline. These findings suggest that HistoPerm can be a valuable tool for improving representation learning of histopathology features when access to labeled data is limited and can lead to whole-slide classification results that are comparable to or superior to fully supervised methods.
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spelling pubmed-103391752023-07-14 HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning DiPalma, Joseph Torresani, Lorenzo Hassanpour, Saeed J Pathol Inform Original Research Article Deep learning has been effective for histology image analysis in digital pathology. However, many current deep learning approaches require large, strongly- or weakly labeled images and regions of interest, which can be time-consuming and resource-intensive to obtain. To address this challenge, we present HistoPerm, a view generation method for representation learning using joint embedding architectures that enhances representation learning for histology images. HistoPerm permutes augmented views of patches extracted from whole-slide histology images to improve classification performance. We evaluated the effectiveness of HistoPerm on 2 histology image datasets for Celiac disease and Renal Cell Carcinoma, using 3 widely used joint embedding architecture-based representation learning methods: BYOL, SimCLR, and VICReg. Our results show that HistoPerm consistently improves patch- and slide-level classification performance in terms of accuracy, F1-score, and AUC. Specifically, for patch-level classification accuracy on the Celiac disease dataset, HistoPerm boosts BYOL and VICReg by 8% and SimCLR by 3%. On the Renal Cell Carcinoma dataset, patch-level classification accuracy is increased by 2% for BYOL and VICReg, and by 1% for SimCLR. In addition, on the Celiac disease dataset, models with HistoPerm outperform the fully supervised baseline model by 6%, 5%, and 2% for BYOL, SimCLR, and VICReg, respectively. For the Renal Cell Carcinoma dataset, HistoPerm lowers the classification accuracy gap for the models up to 10% relative to the fully supervised baseline. These findings suggest that HistoPerm can be a valuable tool for improving representation learning of histopathology features when access to labeled data is limited and can lead to whole-slide classification results that are comparable to or superior to fully supervised methods. Elsevier 2023-07-04 /pmc/articles/PMC10339175/ /pubmed/37457594 http://dx.doi.org/10.1016/j.jpi.2023.100320 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research Article
DiPalma, Joseph
Torresani, Lorenzo
Hassanpour, Saeed
HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning
title HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning
title_full HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning
title_fullStr HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning
title_full_unstemmed HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning
title_short HistoPerm: A permutation-based view generation approach for improving histopathologic feature representation learning
title_sort histoperm: a permutation-based view generation approach for improving histopathologic feature representation learning
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339175/
https://www.ncbi.nlm.nih.gov/pubmed/37457594
http://dx.doi.org/10.1016/j.jpi.2023.100320
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