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Classification of normal versus malignant cells in B-ALL microscopic images based on a tiled convolution neural network approach.

In: Lecture Notes in Bioengineering. 2019. 103-111
DOI
In this paper we present a method based on the existing convolution neural network architecture of AlexNet for the purpose of classifying microscopic images of B-ALL white blood cancer cells. This classification problem is especially challenging due to lack of conspicuous morphological differences between normal and malignant cell nuclei. Therefore, we designed a machine learning pipeline that focused on the texture of the staining images. Briefly, our approach divides the cell image into several overlapping tiles and trains a modified version of AlexNet on the tiles. Only those tiles are retained which are fully contained within the cell image. Several such networks were trained in an ensemble fashion using different training–validation data splits. For a given test image, the tiles are generated and ran through all the trained networks. The outputs of all networks along with the nucleus area are then fed into a simple decision tree, which generates the final prediction. The proposed method was developed in the context of the ISBI 2019 C-NMC challenge. The final testing results demonstrated a classification-weighted F1 score of 0.8307 using 2586 test images. The results demonstrate the possibility of making relatively accurate predictions using only local texture features.
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Publikationstyp Artikel: Sammelbandbeitrag/Buchkapitel
Schlagwörter Acute Lymphoblastic Leukemia ; Cell Classification ; Convolution Neural Network ; Deep Learning ; Machine Learning
Sprache englisch
Veröffentlichungsjahr 2019
HGF-Berichtsjahr 2019
ISSN (print) / ISBN 2195-271X
e-ISSN 2195-2728
Bandtitel Lecture Notes in Bioengineering
Quellenangaben Band: , Heft: , Seiten: 103-111 Artikelnummer: , Supplement: ,
POF Topic(s) 30205 - Bioengineering and Digital Health
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-505500-001
Scopus ID 85076977729
Erfassungsdatum 2020-01-20