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A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images
Whole slide images (WSIs) are digitized histopathology images. WSIs are stored in a pyramidal data structure that contains the same images at multiple magnification levels. In digital pathology, most algorithmic approaches to analyze WSIs use a single magnification level. However, images at differen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289164/ https://www.ncbi.nlm.nih.gov/pubmed/35859771 http://dx.doi.org/10.3389/fpubh.2022.892658 |
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author | D'Amato, Marina Szostak, Przemysław Torben-Nielsen, Benjamin |
author_facet | D'Amato, Marina Szostak, Przemysław Torben-Nielsen, Benjamin |
author_sort | D'Amato, Marina |
collection | PubMed |
description | Whole slide images (WSIs) are digitized histopathology images. WSIs are stored in a pyramidal data structure that contains the same images at multiple magnification levels. In digital pathology, most algorithmic approaches to analyze WSIs use a single magnification level. However, images at different magnification levels may reveal relevant and distinct properties in the image, such as global context or detailed spatial arrangement. Given their high resolution, WSIs cannot be processed as a whole and are broken down into smaller pieces called tiles. Then, a prediction at the tile-level is made for each tile in the larger image. As many classification problems require a prediction at a slide-level, there exist common strategies to integrate the tile-level insights into a slide-level prediction. We explore two approaches to tackle this problem, namely a multiple instance learning framework and a representation learning algorithm (the so-called “barcode approach”) based on clustering. In this work, we apply both approaches in a single- and multi-scale setting and compare the results in a multi-label histopathology classification task to show the promises and pitfalls of multi-scale analysis. Our work shows a consistent improvement in performance of the multi-scale models over single-scale ones. Using multiple instance learning and the barcode approach we achieved a 0.06 and 0.06 improvement in F1 score, respectively, highlighting the importance of combining multiple scales to integrate contextual and detailed information. |
format | Online Article Text |
id | pubmed-9289164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92891642022-07-19 A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images D'Amato, Marina Szostak, Przemysław Torben-Nielsen, Benjamin Front Public Health Public Health Whole slide images (WSIs) are digitized histopathology images. WSIs are stored in a pyramidal data structure that contains the same images at multiple magnification levels. In digital pathology, most algorithmic approaches to analyze WSIs use a single magnification level. However, images at different magnification levels may reveal relevant and distinct properties in the image, such as global context or detailed spatial arrangement. Given their high resolution, WSIs cannot be processed as a whole and are broken down into smaller pieces called tiles. Then, a prediction at the tile-level is made for each tile in the larger image. As many classification problems require a prediction at a slide-level, there exist common strategies to integrate the tile-level insights into a slide-level prediction. We explore two approaches to tackle this problem, namely a multiple instance learning framework and a representation learning algorithm (the so-called “barcode approach”) based on clustering. In this work, we apply both approaches in a single- and multi-scale setting and compare the results in a multi-label histopathology classification task to show the promises and pitfalls of multi-scale analysis. Our work shows a consistent improvement in performance of the multi-scale models over single-scale ones. Using multiple instance learning and the barcode approach we achieved a 0.06 and 0.06 improvement in F1 score, respectively, highlighting the importance of combining multiple scales to integrate contextual and detailed information. Frontiers Media S.A. 2022-07-04 /pmc/articles/PMC9289164/ /pubmed/35859771 http://dx.doi.org/10.3389/fpubh.2022.892658 Text en Copyright © 2022 D'Amato, Szostak and Torben-Nielsen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Public Health D'Amato, Marina Szostak, Przemysław Torben-Nielsen, Benjamin A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images |
title | A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images |
title_full | A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images |
title_fullStr | A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images |
title_full_unstemmed | A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images |
title_short | A Comparison Between Single- and Multi-Scale Approaches for Classification of Histopathology Images |
title_sort | comparison between single- and multi-scale approaches for classification of histopathology images |
topic | Public Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289164/ https://www.ncbi.nlm.nih.gov/pubmed/35859771 http://dx.doi.org/10.3389/fpubh.2022.892658 |
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