面部分析技术在临床遗传学中的应用:对不同人群的考虑。

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY
Paul Kruszka, Cedrik Tekendo-Ngongang
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引用次数: 0

摘要

罕见病的面部分析技术有可能为医生提供有价值的诊断工具,从而缩短诊断之旅。鉴于大多数临床遗传资源都集中在欧洲血统的人群中,我们比较了不同人群遗传综合征的颅面特征,并回顾了机器学习算法在诊断地理和种族多样人群遗传综合症方面的表现。我们还讨论了来自祖先不同背景的群体在机器学习算法训练集中的价值。最后,这篇综述表明,在不同的人群群体中,机器学习模型具有卓越的准确性,这得到了大于0.9的曲线下面积值的支持。人工智能在不同人群中诊断罕见病方面还处于起步阶段,随着对更大、更多样的训练集(包括更广泛的年龄段,尤其是婴儿)的研究,人工智能将变得更加准确。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of facial analysis Technology in Clinical Genetics: Considerations for diverse populations

Facial analysis technology in rare diseases has the potential to shorten the diagnostic odyssey by providing physicians with a valuable diagnostic tool. Given that most clinical genetic resources focus on populations of European descent, we compare craniofacial features in genetic syndromes across different populations and review how machine learning algorithms perform on diagnosing genetic syndromes in geographically and ethnically diverse populations. We also discuss the value of populations from ancestrally diverse backgrounds in the training set of machine learning algorithms. Finally, this review demonstrates that across diverse population groups, machine learning models have outstanding accuracy as supported by the area under the curve values greater than 0.9. Artificial intelligence is only in its infancy in the diagnosis of rare disease in diverse populations and will become more accurate as larger and more diverse training sets, including a wider spectrum of ages, particularly infants, are studied.

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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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