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Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification

MOTIVATION: Multiple instance learning (MIL) is a powerful technique to classify whole slide images (WSIs) for diagnostic pathology. The key challenge of MIL on WSI classification is to discover the critical instances that trigger the bag label. However, tumor heterogeneity significantly hinders the...

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Autores principales: Wang, Zhikang, Bi, Yue, Pan, Tong, Wang, Xiaoyu, Bain, Chris, Bassed, Richard, Imoto, Seiya, Yao, Jianhua, Daly, Roger J, Song, Jiangning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023223/
https://www.ncbi.nlm.nih.gov/pubmed/36864612
http://dx.doi.org/10.1093/bioinformatics/btad114
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author Wang, Zhikang
Bi, Yue
Pan, Tong
Wang, Xiaoyu
Bain, Chris
Bassed, Richard
Imoto, Seiya
Yao, Jianhua
Daly, Roger J
Song, Jiangning
author_facet Wang, Zhikang
Bi, Yue
Pan, Tong
Wang, Xiaoyu
Bain, Chris
Bassed, Richard
Imoto, Seiya
Yao, Jianhua
Daly, Roger J
Song, Jiangning
author_sort Wang, Zhikang
collection PubMed
description MOTIVATION: Multiple instance learning (MIL) is a powerful technique to classify whole slide images (WSIs) for diagnostic pathology. The key challenge of MIL on WSI classification is to discover the critical instances that trigger the bag label. However, tumor heterogeneity significantly hinders the algorithm’s performance. RESULTS: Here, we propose a novel multiplex-detection-based multiple instance learning (MDMIL) which targets tumor heterogeneity by multiplex detection strategy and feature constraints among samples. Specifically, the internal query generated after the probability distribution analysis and the variational query optimized throughout the training process are utilized to detect potential instances in the form of internal and external assistance, respectively. The multiplex detection strategy significantly improves the instance-mining capacity of the deep neural network. Meanwhile, a memory-based contrastive loss is proposed to reach consistency on various phenotypes in the feature space. The novel network and loss function jointly achieve high robustness towards tumor heterogeneity. We conduct experiments on three computational pathology datasets, e.g. CAMELYON16, TCGA-NSCLC, and TCGA-RCC. Benchmarking experiments on the three datasets illustrate that our proposed MDMIL approach achieves superior performance over several existing state-of-the-art methods. AVAILABILITY AND IMPLEMENTATION: MDMIL is available for academic purposes at https://github.com/ZacharyWang-007/MDMIL.
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spelling pubmed-100232232023-03-18 Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification Wang, Zhikang Bi, Yue Pan, Tong Wang, Xiaoyu Bain, Chris Bassed, Richard Imoto, Seiya Yao, Jianhua Daly, Roger J Song, Jiangning Bioinformatics Original Paper MOTIVATION: Multiple instance learning (MIL) is a powerful technique to classify whole slide images (WSIs) for diagnostic pathology. The key challenge of MIL on WSI classification is to discover the critical instances that trigger the bag label. However, tumor heterogeneity significantly hinders the algorithm’s performance. RESULTS: Here, we propose a novel multiplex-detection-based multiple instance learning (MDMIL) which targets tumor heterogeneity by multiplex detection strategy and feature constraints among samples. Specifically, the internal query generated after the probability distribution analysis and the variational query optimized throughout the training process are utilized to detect potential instances in the form of internal and external assistance, respectively. The multiplex detection strategy significantly improves the instance-mining capacity of the deep neural network. Meanwhile, a memory-based contrastive loss is proposed to reach consistency on various phenotypes in the feature space. The novel network and loss function jointly achieve high robustness towards tumor heterogeneity. We conduct experiments on three computational pathology datasets, e.g. CAMELYON16, TCGA-NSCLC, and TCGA-RCC. Benchmarking experiments on the three datasets illustrate that our proposed MDMIL approach achieves superior performance over several existing state-of-the-art methods. AVAILABILITY AND IMPLEMENTATION: MDMIL is available for academic purposes at https://github.com/ZacharyWang-007/MDMIL. Oxford University Press 2023-03-02 /pmc/articles/PMC10023223/ /pubmed/36864612 http://dx.doi.org/10.1093/bioinformatics/btad114 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Wang, Zhikang
Bi, Yue
Pan, Tong
Wang, Xiaoyu
Bain, Chris
Bassed, Richard
Imoto, Seiya
Yao, Jianhua
Daly, Roger J
Song, Jiangning
Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification
title Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification
title_full Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification
title_fullStr Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification
title_full_unstemmed Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification
title_short Targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification
title_sort targeting tumor heterogeneity: multiplex-detection-based multiple instance learning for whole slide image classification
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023223/
https://www.ncbi.nlm.nih.gov/pubmed/36864612
http://dx.doi.org/10.1093/bioinformatics/btad114
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