You are in:Home/Publications/Mona S Al-Kharraz, Lamiaa A. Elrefaei, and Mai A Fadel, " Automated system for chromosome karyotyping to recognize the most common numerical abnormalities using deep learning", IEEE Access, Vol.8, No.1, pp. 157727 - 157747, August 2020, DOI: 10.1109/ACCESS.2020.3019937

Prof. Lamiaa Abdallah Ahmed Elrefaei :: Publications:

Title:
Mona S Al-Kharraz, Lamiaa A. Elrefaei, and Mai A Fadel, " Automated system for chromosome karyotyping to recognize the most common numerical abnormalities using deep learning", IEEE Access, Vol.8, No.1, pp. 157727 - 157747, August 2020, DOI: 10.1109/ACCESS.2020.3019937
Authors: Mona S Al-Kharraz, Lamiaa A. Elrefaei, and Mai A Fadel
Year: 2020
Keywords: Not Available
Journal: IEEE Access
Volume: 8
Issue: 1
Pages: 157727 - 157747
Publisher: IEEE
Local/International: International
Paper Link:
Full paper Not Available
Supplementary materials Not Available
Abstract:

Chromosome analysis is an essential task in a cytogenetics lab, where cytogeneticists can diagnose whether there are abnormalities or not. Karyotyping is a standard technique in chromosome analysis that classifies metaphase image to 24 chromosome classes. The main two categories of chromosome abnormalities are structural abnormalities that are changing in the structure of chromosomes and numerical abnormalities which include either monosomy (missing one chromosome) or trisomy (extra copy of the chromosome). Manual karyotyping is complex and requires high domain expertise, as it takes an amount of time. With these motivations, in this research, we used deep learning to automate karyotyping to recognize the common numerical abnormalities on a dataset containing 147 non-overlapped metaphase images collected from the Center of Excellence in Genomic Medicine Research at King Abdulaziz University. The metaphase images went through three stages. The first one is individual chromosomes detection using YOLOv2 Convolutional Neural Network followed by some chromosome post-processing. This step achieved 0.84 mean IoU, 0.9923 AP, and 100% individual chromosomes detection accuracy. The second stage is feature extraction and classification where we fine-tune VGG19 network using two different approaches, one by adding extra fully connected layer(s) and another by replacing fully connected layers with the global average pooling layer. The best accuracy obtained is 95.04%. The final step is detecting abnormality and this step obtained 96.67% abnormality detection accuracy. To further validate the proposed classification method, we examined the Biomedical Imaging Laboratory dataset which is publicly available online and achieved 94.11% accuracy.

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