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Optimal designs to select individuals for genotyping conditional on observed binary or survival outcomes and non-genetic covariates

机译:根据观察到的二进制或生存结果以及非遗传协变量选择个体进行基因分型的最佳设计

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摘要

In gene-disease association studies, the cost of genotyping makes it economical to use a two-stage design where only a subset of the cohort is genotyped. At the first-stage. the follow-up data along with some risk factors or non-genetic covariates are collected for the cohort and a subset of the cohort is then selected for genotyping at the second-stage. Intuitively the selection of the subset for the second-stage could be carried out efficiently if the data collected at the first-stage are utilized. The information contained in the conditional probability of the genotype given the first-stage, data and the initial estimates of the parameters of interest is being maximized for efficient selection of the subset. The proposed selection method is illustrated using the logistic regression and Cox's proportional hazards model and algorithms that can find optimal or nearly optimal designs in discrete design space are presented. Simulation comparisons between D-optimal design, extreme selection and case-cohort design suggest that D-optimal design is the most efficient in terms of variance of estimated parameters, but extreme selection may be a good alternative for practical study design.
机译:在基因疾病关联研究中,基因分型的成本使得使用只有两个人的子集进行基因分型的两阶段设计变得经济。在第一阶段。随后收集该队列的随访数据以及一些风险因素或非遗传协变量,然后在第二阶段选择该队列的一个子集进行基因分型。如果利用在第一阶段收集的数据,则可以有效地直观地选择第二阶段的子集。给定第一阶段的基因型的条件概率,感兴趣的参数的数据和初始估计值中包含的信息,可以使子集的有效选择最大化。通过逻辑回归和Cox比例风险模型说明了提出的选择方法,并提出了可以在离散设计空间中找到最佳或接近最佳设计的算法。 D最优设计,极限选择和案例队列设计之间的仿真比较表明,就估计参数的方差而言,D最优设计是最有效的,但是极限选择对于实际的研究设计可能是一个很好的选择。

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