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Cited 15 time in webofscience Cited 18 time in scopus
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Deep Features Aggregation-Based Joint Segmentation of Cytoplasm and Nuclei in White Blood Cells

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dc.contributor.authorHaider, Adnan-
dc.contributor.authorArsalan, Muhammad-
dc.contributor.authorLee, Young Won-
dc.contributor.authorPark, Kang Ryoung-
dc.date.accessioned2023-04-27T10:40:37Z-
dc.date.available2023-04-27T10:40:37Z-
dc.date.issued2022-08-
dc.identifier.issn2168-2194-
dc.identifier.issn2168-2208-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/2811-
dc.description.abstractWhite blood cells (WBCs), also known as leukocytes, are one of the valuable parts of the blood and immune system. Typically, pathologists use microscope for the manual inspection of blood smears which is a time-consuming, error-prone, and labor-intensive procedure. To address these issues, we present two novel shallow networks: a leukocyte deep segmentation network (LDS-Net) and leukocyte deep aggregation segmentation network (LDAS-Net) for the joint segmentation of cytoplasm and nuclei in WBC images. LDS-Net is a shallow architecture with three downsampling stages and seven convolution layers. LDAS-Net is an extended version of LDS-Net that utilizes a novel pool-less low-level information transfer bridge to transfer low-level information to the deep layers of the network. This information is aggregated with deep features in a dense feature concatenation block to achieve accurate cytoplasm and nuclei joint segmentation. We evaluated our developed architectures on four WBC publicly available datasets. For cytoplasmic segmentation in WBCs, the proposed method achieved the dice coefficients of 98.97%, 99.0%, 96.05%, and 98.79% on Datasets 1, 2, 3, and 4, respectively. For nuclei segmentation, the dice coefficients of 96.35% and 98.09% are achieved for Datasets 1 and 2, respectively. Proposed method outperforms state-of-the-art methods with superior computational efficiency and requires only 6.5 million trainable parameters.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherIEEE-
dc.titleDeep Features Aggregation-Based Joint Segmentation of Cytoplasm and Nuclei in White Blood Cells-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1109/JBHI.2022.3178765-
dc.identifier.scopusid2-s2.0-85131758330-
dc.identifier.wosid000841851000014-
dc.identifier.bibliographicCitationIEEE Journal of Biomedical and Health Informatics, v.26, no.8, pp 3685 - 3696-
dc.citation.titleIEEE Journal of Biomedical and Health Informatics-
dc.citation.volume26-
dc.citation.number8-
dc.citation.startPage3685-
dc.citation.endPage3696-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaComputer Science-
dc.relation.journalResearchAreaMathematical & Computational Biology-
dc.relation.journalResearchAreaMedical Informatics-
dc.relation.journalWebOfScienceCategoryComputer Science, Information Systems-
dc.relation.journalWebOfScienceCategoryComputer Science, Interdisciplinary Applications-
dc.relation.journalWebOfScienceCategoryMathematical & Computational Biology-
dc.relation.journalWebOfScienceCategoryMedical Informatics-
dc.subject.keywordPlusIMAGES-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordAuthorImage segmentation-
dc.subject.keywordAuthorFeature extraction-
dc.subject.keywordAuthorVisualization-
dc.subject.keywordAuthorBlood-
dc.subject.keywordAuthorBioinformatics-
dc.subject.keywordAuthorComputer architecture-
dc.subject.keywordAuthorTask analysis-
dc.subject.keywordAuthorDeep learning-
dc.subject.keywordAuthorartificial intelligence-
dc.subject.keywordAuthorWBC segmentation-
dc.subject.keywordAuthorcytoplasm and nuclei joint segmentation-
dc.subject.keywordAuthorfeatures aggregation-
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