贝叶斯概率
孟德尔遗传
医学遗传学
孟德尔随机化
可能性
生物
基因组学
贝叶斯定理
计算机科学
计算生物学
点(几何)
生物信息学
遗传学
人工智能
机器学习
基因组
数学
基因
遗传变异
逻辑回归
基因型
几何学
作者
Sean V. Tavtigian,Steven M. Harrison,Kenneth M. Boucher,Leslie G. Biesecker
出处
期刊:Human Mutation
[Wiley]
日期:2020-07-28
卷期号:41 (10): 1734-1737
被引量:139
摘要
Recently, we demonstrated that the qualitative American College of Medical Genetics and Genomics/Association for Medical Pathology (ACMG/AMP) guidelines for evaluation of Mendelian disease gene variants are fundamentally compatible with a quantitative Bayesian formulation. Here, we show that the underlying ACMG/AMP “strength of evidence categories” can be abstracted into a point system. These points are proportional to Log(odds), are additive, and produce a system that recapitulates the Bayesian formulation of the ACMG/AMP guidelines. The strengths of this system are its simplicity and that the connection between point values and odds of pathogenicity allows empirical calibration of the strength of evidence for individual data types. Weaknesses include that a narrow range of prior probabilities is locked in and that the Bayesian nature of the system is inapparent. We conclude that a points-based system has the practical attribute of user-friendliness and can be useful so long as the underlying Bayesian principles are acknowledged.
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