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首页> 外文期刊>Annals of Human Genetics >Optimal Robust Two-Stage Designs for Genome-Wide Association Studies
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Optimal Robust Two-Stage Designs for Genome-Wide Association Studies

机译:全基因组关联研究的最佳鲁棒两阶段设计

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Optimal robust two-stage designs for genome-wide association studies are proposed using the maximum of the recessive, additive and dominant linear trend test statistics. These designs combine cost-saving two-stage genotyping with robustness against misspecification of the genetic model and are much more efficient than designs based on a single model specific test statistic in detecting multiple loci with different modes of inheritance. For given power of 90%, typical cost savings of 34% can be realised by increasing the total sample size by about 13% but genotyping only about half of the sample for the full marker set in the first stage and carrying forward about 0.06% of the markers to the second stage analysis. We also present robust two-stage designs providing optimal allocation of a limited budget for pre-existing samples. If a sample is available which would yield a power of 90% when fully genotyped, genotyping only half of the sample due to a limited budget will typically cause a loss of power of more than 55%. Using an optimal two-stage approach in the same sample under the same budget restrictions will limit the loss of power to less than 10%. In general, the optimal proportion of markers to be followed up in the second stage strongly depends on the cost ratio for chips and individual genotyping, while the design parameters of the optimal designs (total sample size, first stage proportion, first and second stage significance limit) do not much depend on the genetic model assumptions.
机译:使用最大的隐性,加性和显性线性趋势测试统计数据,提出了用于全基因组关联研究的最佳鲁棒两阶段设计。这些设计将节省成本的两阶段基因分型与针对遗传模型错误指定的鲁棒性相结合,并且比基于单个模型特定测试统计的设计在检测具有不同遗传模式的多个基因座时要有效得多。对于给定的90%功效,可以通过将总样本量增加约13%,但在第一阶段对完整标记集进行基因分型仅对样本的一半进行基因分型,并结转约0.06%的样本,从而实现34%的典型成本节省。第二阶段分析的标记。我们还提出了可靠的两阶段设计,可为有限的预算为现有样本提供最佳分配。如果有一个样本,在进行完全基因分型时将产生90%的功效,由于预算有限,仅对样本的一半进行基因分型通常会导致超过55%的功效损失。在相同的预算限制下,在同一样本中使用最优的两阶段方法将功耗损失限制在10%以下。一般而言,第二阶段要跟进的标记物的最佳比例在很大程度上取决于芯片的成本比和个体基因分型,而最佳设计的设计参数(总样本量,第一阶段比例,第一阶段和第二阶段的重要性)极限)并不太取决于遗传模型的假设。

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