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Cited 24 time in webofscience Cited 27 time in scopus
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Accurate Segmentation of Nuclear Regions with Multi-Organ Histopathology Images Using Artificial Intelligence for Cancer Diagnosis in Personalized Medicineopen access

Authors
Mahmood, TahirOwais, MuhammadNoh, Kyoung JunYoon, Hyo SikKoo, Ja HyungHaider, AdnanSultan, HaseebPark, Kang Ryoung
Issue Date
Jun-2021
Publisher
MDPI
Keywords
multi-organ histopathology images; triple-negative breast cancer; The Cancer Genome Atlas; artificial intelligence; nuclear segmentation; stain normalization; cancer grading and prognosis
Citation
JOURNAL OF PERSONALIZED MEDICINE, v.11, no.6
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF PERSONALIZED MEDICINE
Volume
11
Number
6
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/17887
DOI
10.3390/jpm11060515
ISSN
2075-4426
2075-4426
Abstract
Accurate nuclear segmentation in histopathology images plays a key role in digital pathology. It is considered a prerequisite for the determination of cell phenotype, nuclear morphometrics, cell classification, and the grading and prognosis of cancer. However, it is a very challenging task because of the different types of nuclei, large intraclass variations, and diverse cell morphologies. Consequently, the manual inspection of such images under high-resolution microscopes is tedious and time-consuming. Alternatively, artificial intelligence (AI)-based automated techniques, which are fast and robust, and require less human effort, can be used. Recently, several AI-based nuclear segmentation techniques have been proposed. They have shown a significant performance improvement for this task, but there is room for further improvement. Thus, we propose an AI-based nuclear segmentation technique in which we adopt a new nuclear segmentation network empowered by residual skip connections to address this issue. Experiments were performed on two publicly available datasets: (1) The Cancer Genome Atlas (TCGA), and (2) Triple-Negative Breast Cancer (TNBC). The results show that our proposed technique achieves an aggregated Jaccard index (AJI) of 0.6794, Dice coefficient of 0.8084, and F1-measure of 0.8547 on TCGA dataset, and an AJI of 0.7332, Dice coefficient of 0.8441, precision of 0.8352, recall of 0.8306, and F1-measure of 0.8329 on the TNBC dataset. These values are higher than those of the state-of-the-art methods.
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