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dc.contributor.authorAbou Ali, Mohamad
dc.contributor.authorDornaika, Fadi
dc.contributor.authorArganda Carreras, Ignacio
dc.date.accessioned2024-02-01T19:21:08Z
dc.date.available2024-02-01T19:21:08Z
dc.date.issued2023-12-10
dc.identifier.citationAlgorithms 16(12) : (2023) // Article ID 562es_ES
dc.identifier.issn1999-4893
dc.identifier.urihttp://hdl.handle.net/10810/64569
dc.description.abstractArtificial intelligence (AI) has emerged as a cutting-edge tool, simultaneously accelerating, securing, and enhancing the diagnosis and treatment of patients. An exemplification of this capability is evident in the analysis of peripheral blood smears (PBS). In university medical centers, hematologists routinely examine hundreds of PBS slides daily to validate or correct outcomes produced by advanced hematology analyzers assessing samples from potentially problematic patients. This process may logically lead to erroneous PBC readings, posing risks to patient health. AI functions as a transformative tool, significantly improving the accuracy and precision of readings and diagnoses. This study reshapes the parameters of blood cell classification, harnessing the capabilities of AI and broadening the scope from 5 to 11 specific blood cell categories with the challenging 11-class PBC dataset. This transformation facilitates a more profound exploration of blood cell diversity, surpassing prior constraints in medical image analysis. Our approach combines state-of-the-art deep learning techniques, including pre-trained ConvNets, ViTb16 models, and custom CNN architectures. We employ transfer learning, fine-tuning, and ensemble strategies, such as CBAM and Averaging ensembles, to achieve unprecedented accuracy and interpretability. Our fully fine-tuned EfficientNetV2 B0 model sets a new standard, with a macro-average precision, recall, and F1-score of 91%, 90%, and 90%, respectively, and an average accuracy of 93%. This breakthrough underscores the transformative potential of 11-class blood cell classification for more precise medical diagnoses. Moreover, our groundbreaking “Naturalize” augmentation technique produces remarkable results. The 2K-PBC dataset generated with “Naturalize” boasts a macro-average precision, recall, and F1-score of 97%, along with an average accuracy of 96% when leveraging the fully fine-tuned EfficientNetV2 B0 model. This innovation not only elevates classification performance but also addresses data scarcity and bias in medical deep learning. Our research marks a paradigm shift in blood cell classification, enabling more nuanced and insightful medical analyses. The “Naturalize” technique’s impact extends beyond blood cell classification, emphasizing the vital role of diverse and comprehensive datasets in advancing healthcare applications through deep learning.es_ES
dc.description.sponsorshipThis work is supported by grant PID2021-126701OB-I00 funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”, and by grant GIU19/027 funded by the University of the Basque Country UPV/EHU.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2021-126701OB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/es/
dc.subjectconvolutional neural net (CNN)es_ES
dc.subjectvision transformer (ViT)es_ES
dc.subjectImageNet modelses_ES
dc.subjecttransfer learning (TL)es_ES
dc.subjectmachine learning (ML)es_ES
dc.subjectdeep learning (DP)es_ES
dc.subjectblood cell classificationes_ES
dc.subjectperipheral blood cell (PBC)es_ES
dc.subjectCBAMes_ES
dc.subjectNaturalizees_ES
dc.titleBlood Cell Revolution: Unveiling 11 Distinct Types with ‘Naturalize’ Augmentationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2023-12-22T13:45:53Z
dc.rights.holder© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1999-4893/16/12/562es_ES
dc.identifier.doi10.3390/a16120562
dc.departamentoesCiencia de la computación e inteligencia artificial
dc.departamentoeuKonputagailuen Arkitektura eta Teknologia


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© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).
Except where otherwise noted, this item's license is described as © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).