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Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis
Objective and Impact Statement. We present a fully automated hematological analysis framework based on single-channel (single-wavelength), label-free deep-ultraviolet (UV) microscopy that serves as a fast, cost-effective alternative to conventional hematology analyzers. Introduction. Hematological a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AAAS
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521747/ https://www.ncbi.nlm.nih.gov/pubmed/37850166 http://dx.doi.org/10.34133/2022/9853606 |
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author | Kaza, Nischita Ojaghi, Ashkan Robles, Francisco E. |
author_facet | Kaza, Nischita Ojaghi, Ashkan Robles, Francisco E. |
author_sort | Kaza, Nischita |
collection | PubMed |
description | Objective and Impact Statement. We present a fully automated hematological analysis framework based on single-channel (single-wavelength), label-free deep-ultraviolet (UV) microscopy that serves as a fast, cost-effective alternative to conventional hematology analyzers. Introduction. Hematological analysis is essential for the diagnosis and monitoring of several diseases but requires complex systems operated by trained personnel, costly chemical reagents, and lengthy protocols. Label-free techniques eliminate the need for staining or additional preprocessing and can lead to faster analysis and a simpler workflow. In this work, we leverage the unique capabilities of deep-UV microscopy as a label-free, molecular imaging technique to develop a deep learning-based pipeline that enables virtual staining, segmentation, classification, and counting of white blood cells (WBCs) in single-channel images of peripheral blood smears. Methods. We train independent deep networks to virtually stain and segment grayscale images of smears. The segmented images are then used to train a classifier to yield a quantitative five-part WBC differential. Results. Our virtual staining scheme accurately recapitulates the appearance of cells under conventional Giemsa staining, the gold standard in hematology. The trained cellular and nuclear segmentation networks achieve high accuracy, and the classifier can achieve a quantitative five-part differential on unseen test data. Conclusion. This proposed automated hematology analysis framework could greatly simplify and improve current complete blood count and blood smear analysis and lead to the development of a simple, fast, and low-cost, point-of-care hematology analyzer. |
format | Online Article Text |
id | pubmed-10521747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AAAS |
record_format | MEDLINE/PubMed |
spelling | pubmed-105217472023-10-17 Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis Kaza, Nischita Ojaghi, Ashkan Robles, Francisco E. BME Front Research Article Objective and Impact Statement. We present a fully automated hematological analysis framework based on single-channel (single-wavelength), label-free deep-ultraviolet (UV) microscopy that serves as a fast, cost-effective alternative to conventional hematology analyzers. Introduction. Hematological analysis is essential for the diagnosis and monitoring of several diseases but requires complex systems operated by trained personnel, costly chemical reagents, and lengthy protocols. Label-free techniques eliminate the need for staining or additional preprocessing and can lead to faster analysis and a simpler workflow. In this work, we leverage the unique capabilities of deep-UV microscopy as a label-free, molecular imaging technique to develop a deep learning-based pipeline that enables virtual staining, segmentation, classification, and counting of white blood cells (WBCs) in single-channel images of peripheral blood smears. Methods. We train independent deep networks to virtually stain and segment grayscale images of smears. The segmented images are then used to train a classifier to yield a quantitative five-part WBC differential. Results. Our virtual staining scheme accurately recapitulates the appearance of cells under conventional Giemsa staining, the gold standard in hematology. The trained cellular and nuclear segmentation networks achieve high accuracy, and the classifier can achieve a quantitative five-part differential on unseen test data. Conclusion. This proposed automated hematology analysis framework could greatly simplify and improve current complete blood count and blood smear analysis and lead to the development of a simple, fast, and low-cost, point-of-care hematology analyzer. AAAS 2022-07-01 /pmc/articles/PMC10521747/ /pubmed/37850166 http://dx.doi.org/10.34133/2022/9853606 Text en Copyright © 2022 Nischita Kaza et al. https://creativecommons.org/licenses/by/4.0/Exclusive Licensee Suzhou Institute of Biomedical Engineering and Technology, CAS. Distributed under a Creative Commons Attribution License (CC BY 4.0). (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Research Article Kaza, Nischita Ojaghi, Ashkan Robles, Francisco E. Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis |
title | Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis |
title_full | Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis |
title_fullStr | Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis |
title_full_unstemmed | Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis |
title_short | Virtual Staining, Segmentation, and Classification of Blood Smears for Label-Free Hematology Analysis |
title_sort | virtual staining, segmentation, and classification of blood smears for label-free hematology analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521747/ https://www.ncbi.nlm.nih.gov/pubmed/37850166 http://dx.doi.org/10.34133/2022/9853606 |
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