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Label‐Free Identification of White Blood Cells Using Machine Learning

Mariam Nassar, Minh Doan, Andrew Filby, Olaf Wolkenhauer, Darin K. Fogg, Justyna Piasecka, Cathy Thornton Orcid Logo, Anne E. Carpenter, Huw Summers Orcid Logo, Paul Rees Orcid Logo, Holger Hennig

Cytometry Part A

Swansea University Authors: Cathy Thornton Orcid Logo, Huw Summers Orcid Logo, Paul Rees Orcid Logo

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DOI (Published version): 10.1002/cyto.a.23794

Abstract

White blood cell (WBC) differential counting is an established clinical routine to assess patient immune system status. Fluorescent markers and a flow cytometer are required for the current state-of-the-art method for determining WBC differential counts. However, this process requires several sample...

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Published in: Cytometry Part A
ISSN: 1552-4922 1552-4930
Published: 2019
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URI: https://cronfa.swan.ac.uk/Record/cronfa50355
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spelling 2019-05-29T12:06:42.1838656 v2 50355 2019-05-14 Label‐Free Identification of White Blood Cells Using Machine Learning c71a7a4be7361094d046d312202bce0c 0000-0002-5153-573X Cathy Thornton Cathy Thornton true false a61c15e220837ebfa52648c143769427 0000-0002-0898-5612 Huw Summers Huw Summers true false 537a2fe031a796a3bde99679ee8c24f5 0000-0002-7715-6914 Paul Rees Paul Rees true false 2019-05-14 BMS White blood cell (WBC) differential counting is an established clinical routine to assess patient immune system status. Fluorescent markers and a flow cytometer are required for the current state-of-the-art method for determining WBC differential counts. However, this process requires several sample preparation steps and may adversely disturb the cells. We present a novel label-free approach using an imaging flow cytometer and machine learning algorithms, where live, unstained WBCs were classified. It achieved an average F1-score of 97% and two subtypes of WBCs, B and T lymphocytes, were distinguished from each other with an average F1-score of 78%, a task previously considered impossible for unlabeled samples. We provide an open-source workflow to carry out the procedure. We validated the WBC analysis with unstained samples from 85 donors. The presented method enables robust and highly accurate identification of WBCs, minimizing the disturbance to the cells and leaving marker channels free to answer other biological questions. It also opens the door to employing machine learning for liquid biopsy, here, using the rich information in cell morphology for a wide range of diagnostics of primary blood. Journal Article Cytometry Part A 1552-4922 1552-4930 high-content analysis; imaging flow cytometry; label-free classification; liquid biopsy; lymphocytes; machine learning; personalized medicine; white blood cell count; white blood cells 31 12 2019 2019-12-31 10.1002/cyto.a.23794 COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University 2019-05-29T12:06:42.1838656 2019-05-14T11:04:23.4615650 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Mariam Nassar 1 Minh Doan 2 Andrew Filby 3 Olaf Wolkenhauer 4 Darin K. Fogg 5 Justyna Piasecka 6 Cathy Thornton 0000-0002-5153-573X 7 Anne E. Carpenter 8 Huw Summers 0000-0002-0898-5612 9 Paul Rees 0000-0002-7715-6914 10 Holger Hennig 11 0050355-29052019120538.pdf 50355.pdf 2019-05-29T12:05:38.3800000 Output 2098974 application/pdf Version of Record true 2019-05-28T00:00:00.0000000 Released under the terms of a Creative Commons Attribution License (CC-BY). true eng
title Label‐Free Identification of White Blood Cells Using Machine Learning
spellingShingle Label‐Free Identification of White Blood Cells Using Machine Learning
Cathy Thornton
Huw Summers
Paul Rees
title_short Label‐Free Identification of White Blood Cells Using Machine Learning
title_full Label‐Free Identification of White Blood Cells Using Machine Learning
title_fullStr Label‐Free Identification of White Blood Cells Using Machine Learning
title_full_unstemmed Label‐Free Identification of White Blood Cells Using Machine Learning
title_sort Label‐Free Identification of White Blood Cells Using Machine Learning
author_id_str_mv c71a7a4be7361094d046d312202bce0c
a61c15e220837ebfa52648c143769427
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author_id_fullname_str_mv c71a7a4be7361094d046d312202bce0c_***_Cathy Thornton
a61c15e220837ebfa52648c143769427_***_Huw Summers
537a2fe031a796a3bde99679ee8c24f5_***_Paul Rees
author Cathy Thornton
Huw Summers
Paul Rees
author2 Mariam Nassar
Minh Doan
Andrew Filby
Olaf Wolkenhauer
Darin K. Fogg
Justyna Piasecka
Cathy Thornton
Anne E. Carpenter
Huw Summers
Paul Rees
Holger Hennig
format Journal article
container_title Cytometry Part A
publishDate 2019
institution Swansea University
issn 1552-4922
1552-4930
doi_str_mv 10.1002/cyto.a.23794
college_str Faculty of Medicine, Health and Life Sciences
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hierarchy_top_title Faculty of Medicine, Health and Life Sciences
hierarchy_parent_id facultyofmedicinehealthandlifesciences
hierarchy_parent_title Faculty of Medicine, Health and Life Sciences
department_str Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine
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description White blood cell (WBC) differential counting is an established clinical routine to assess patient immune system status. Fluorescent markers and a flow cytometer are required for the current state-of-the-art method for determining WBC differential counts. However, this process requires several sample preparation steps and may adversely disturb the cells. We present a novel label-free approach using an imaging flow cytometer and machine learning algorithms, where live, unstained WBCs were classified. It achieved an average F1-score of 97% and two subtypes of WBCs, B and T lymphocytes, were distinguished from each other with an average F1-score of 78%, a task previously considered impossible for unlabeled samples. We provide an open-source workflow to carry out the procedure. We validated the WBC analysis with unstained samples from 85 donors. The presented method enables robust and highly accurate identification of WBCs, minimizing the disturbance to the cells and leaving marker channels free to answer other biological questions. It also opens the door to employing machine learning for liquid biopsy, here, using the rich information in cell morphology for a wide range of diagnostics of primary blood.
published_date 2019-12-31T04:01:47Z
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