Artificial intelligence-based approaches for the detection and prioritization of genomic mutations in congenital surgical diseases

被引:4
|
作者
Lin, Qiongfen [1 ]
Tam, Paul Kwong-Hang [1 ,2 ]
Tang, Clara Sze-Man [1 ,3 ]
机构
[1] Univ Hong Kong, Li Ka Shing Fac Med, Dept Surg, Hong Kong, Peoples R China
[2] Macau Univ Sci & Technol, Fac Med, Macau, Peoples R China
[3] Univ Hong Kong, Karolinska Inst Collaborat Regenerat Med, Dr Li Dak Sum Res Ctr, Hong Kong, Peoples R China
来源
FRONTIERS IN PEDIATRICS | 2023年 / 11卷
关键词
artificial intelligence; congenital surgical diseases; variant detection; variant prioritization; bioinformatics; COPY-NUMBER VARIATION; FRAMEWORK; VARIANTS; PATHOGENICITY; GUIDELINES; DISCOVERY;
D O I
10.3389/fped.2023.1203289
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Genetic mutations are critical factors leading to congenital surgical diseases and can be identified through genomic analysis. Early and accurate identification of genetic mutations underlying these conditions is vital for clinical diagnosis and effective treatment. In recent years, artificial intelligence (AI) has been widely applied for analyzing genomic data in various clinical settings, including congenital surgical diseases. This review paper summarizes current state-of-the-art AI-based approaches used in genomic analysis and highlighted some successful applications that deepen our understanding of the etiology of several congenital surgical diseases. We focus on the AI methods designed for the detection of different variant types and the prioritization of deleterious variants located in different genomic regions, aiming to uncover susceptibility genomic mutations contributed to congenital surgical disorders.
引用
收藏
页数:8
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