Please use this identifier to cite or link to this item: https://repositorio.inpa.gov.br/handle/1/36345
Title: First Step of Automated Malaria Diagnosis: Evaluation of Focus Functions in Thick Blood Smear Images
Authors: Costa, Marly Guimarães Fernandes
Almeida, L. N.A.
Guimarães, F. B.
Barbosa, M. G.V.
Ogusku, Maurício Morishi
Costa, João Pedro Guimarães Fernandes
Costa Filho, Cícero Ferreira Fernandes
Keywords: Automation
Biomedical engineering
Diseases
Life cycle
Thick films
Automated microscopy
Automatic focusing
Diagnostic standard
Malaria diagnosis
Plasmodium vivax
Processed images
Thin and thick films
World Health Organization
Blood
Issue Date: 2019
metadata.dc.publisher.journal: IFMBE Proceedings
metadata.dc.relation.ispartof: Volume 70, pgs. 231-237
metadata.dc.description.resumo: According to World Health Organization, light microscopy is the diagnostic standard of malaria. This diagnosis requires examination of both thin and thick films from the same patient. However, in most large health clinics and hospitals, the quality of microscopy-based malaria diagnosis is frequently inadequate. Automatic microscopy diagnosis allows an increase in the number of fields of view to be analyzed, providing more accurate diagnosis, while reducing the time required for that purpose. Automatic focusing of the microscope is an essential component of automated microscopy; it is the first step of automated malaria diagnosis. In this work, we implemented the “classical image-analysis-based auto-focus techniques” approach using nine-focus function in order to identify the best focus function for thick blood smear images. Because some previous works have shown that the accuracy focus functions sometimes depends on content of the processed images, and the specimen can determine which metrics should be more adequate, we proceeded two experiments. In experiment #1, we evaluated the focus functions in an image-stacks dataset (338 stacks and 5 images/stack). Then, we did experiment #2, this time, testing with patch images (fragments) containing Plasmodium vivax in its various life cycle phases (ring or immature trophozoite, ameboid trophozoite, schizont and gametocyte). The parasite dataset used contained 1713 patches. Brenner gradient focus function was the best in both experiments. © 2019, Springer Nature Singapore Pte Ltd.
metadata.dc.identifier.doi: 10.1007/978-981-13-2517-5_36
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