Chromosome analysis method based on deep learning: Counting chromosomes and detecting abnormal chromosomes

被引:5
|
作者
Kang, Seungyoung [1 ]
Han, Junghun [1 ]
Lee, Inkyung [2 ]
Joo, Haemi [2 ]
Chung, Yousun [3 ]
Yang, Sejung [4 ,5 ]
机构
[1] Yonsei Univ, Dept Biomed Engn, Wonju 26493, South Korea
[2] Korea Hydro & Nucl Power, Radiat Hlth Inst, Seoul 04505, South Korea
[3] Kangdong Sacred Heart Hosp, Dept Lab Med, Seoul 05355, South Korea
[4] Yonsei Univ, Wonju Coll Med, Dept Precis Med, Wonju 26426, South Korea
[5] Yonsei Univ, Grad Sch, Dept Med Informat & Biostat, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Chromosome analysis; Counting chromosome; Detecting abnormal chromosome; Object detection; Deep learning; IONIZING-RADIATION; ABERRATIONS; LYMPHOCYTES; POPULATION; EXPOSURE;
D O I
10.1016/j.bspc.2023.105891
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Karyotype analysis is a cytogenetic test method that counts chromosomes and evaluates their structural abnormalities. However, since the processes of counting chromosomes and determining structural abnormalities are mostly performed manually, the analysis is time-consuming and labor-intensive, and the results may vary depending on the expert who performs the analysis. Therefore, studies for automating karyotype analysis have been conducted; however, most have focused on the detection of dicentric chromosomes among abnormal chromosome classes and counting the number of chromosomes. Therefore, this study proposes an automated chromosome analysis system that applies an object detection method based on deep learning to simplify chromosome analysis and derive effective results. The proposed analysis system consists of a chromosome counting system and an abnormal chromosome detection system. Additionally, to further improve the performance of the automated chromosome analysis system, convolutional spatial pooling attention and squeeze and excitation block are applied. In each proposed system, the object detection-based deep learning model detects a chromosome with a probability of 99.32%, and a chromosome abnormality with a probability of approximately 75.71%.
引用
收藏
页数:14
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