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Approximate confidence intervals for risk prediction in genetic counseling.

机译:遗传咨询中的风险预测的近似置信区间。

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摘要

In current genetic counseling practice, a single risk estimate is often quoted to a family rather than a range of risks. Such point estimates are predicated on knowing basic parameters like recombination fractions exactly when, in fact, there may be considerable uncertainty about them. Using the large sample theory of statistics, it is possible to derive approximate risk intervals that incorporate known statistical imprecision. The necessary theory will be briefly discussed and illustrated by an application to family counseling for Duchenne muscular dystrophy in the presence of two flanking markers. Some of the problems of the theory will be mentioned. These include lack of adequate sample size to justify the conclusions of large sample theory, pronounced nonlinearity in the risk function, and failure to take into proper account genetic interference. Except in trivial cases, sophisticated computer software is needed to carry out the computations of risk intervals.
机译:在当前的遗传咨询实践中,通常将单个风险估计数引用给一个家庭,而不是一系列风险。这样的点估计是基于准确地知道基本参数(例如重组分数)的,而实际上实际上可能存在很大的不确定性。使用大样本统计理论,可以得出包含已知统计不准确性的近似风险区间。在存在两个侧翼标记的情况下,将通过在家庭咨询中针对杜兴氏肌营养不良症的应用来简要讨论和说明必要的理论。将提到该理论的一些问题。这些包括缺乏足够的样本量来证明大样本理论的结论,风险函数中明显的非线性以及未能适当考虑遗传干扰。除琐碎的情况外,还需要使用复杂的计算机软件来进行风险区间的计算。

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