Optimization of whole slide imaging scan settings for computer vision using human lung cancer tissue.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 07 05 2024
accepted: 16 08 2024
medline: 9 9 2024
pubmed: 9 9 2024
entrez: 9 9 2024
Statut: epublish

Résumé

Digital pathology has become increasingly popular for research and clinical applications. Using high-quality microscopes to produce Whole Slide Images of tumor tissue enables the discovery of insights into biological aspects invisible to the human eye. These are acquired through downstream analyses using spatial statistics and artificial intelligence. Determination of the quality and consistency of these images is needed to ensure accurate outcomes when identifying clinical and subclinical image features. Additionally, the time-intensive process of generating high-volume images results in a trade-off that needs to be carefully balanced. This study aims to determine optimal instrument settings to generate representative images of pathological tissue using digital microscopy. Using various settings, an H&E stained sample was scanned using the ZEISS Axio Scan.Z1. Next, nucleus segmentation was performed on resulting images using StarDist. Subsequently, detections were compared between scans using a matching algorithm. Finally, nucleus-level information was compared between scans. Results indicated that while general matching percentages were high, similarity between information from replicates was relatively low. Additionally, settings resulting in longer scanning times and increased data volume did not increase similarity between replicates. In conclusion, the scan setting ultimately deemed optimal combined consistent and qualitative performance with low throughput time.

Identifiants

pubmed: 39250489
doi: 10.1371/journal.pone.0309740
pii: PONE-D-24-15290
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0309740

Informations de copyright

Copyright: © 2024 Geubbelmans et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Melvin Geubbelmans (M)

Data Science Institute, Hasselt University, Hasselt, Belgium.

Jari Claes (J)

Data Science Institute, Hasselt University, Hasselt, Belgium.

Kim Nijsten (K)

UHasselt, Lab for Functional Imaging & Research on Stem Cells (FIERCE Lab), BIOMED, Diepenbeek, Belgium.

Pascal Gervois (P)

UHasselt, Lab for Functional Imaging & Research on Stem Cells (FIERCE Lab), BIOMED, Diepenbeek, Belgium.
UHasselt, Limburg Clinical Research Center (LCRC), Hasselt, Belgium.

Simon Appeltans (S)

Data Science Institute, Hasselt University, Hasselt, Belgium.

Sandrina Martens (S)

UHasselt, Lab for Functional Imaging & Research on Stem Cells (FIERCE Lab), BIOMED, Diepenbeek, Belgium.

Esther Wolfs (E)

UHasselt, Lab for Functional Imaging & Research on Stem Cells (FIERCE Lab), BIOMED, Diepenbeek, Belgium.

Michiel Thomeer (M)

UHasselt, Limburg Clinical Research Center (LCRC), Hasselt, Belgium.
Department of Respiratory Medicine, Ziekenhuis Oost-Limburg, Genk, Belgium.

Dirk Valkenborg (D)

Data Science Institute, Hasselt University, Hasselt, Belgium.

Christel Faes (C)

Data Science Institute, Hasselt University, Hasselt, Belgium.

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