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A MINE Alternative to D-Optimal Designs for the Linear Model

机译:线性模型的D优化设计的MINE替代方案

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摘要

Doing large-scale genomics experiments can be expensive, and so experimenters want to get the most information out of each experiment. To this end the Maximally Informative Next Experiment (MINE) criterion for experimental design was developed. Here we explore this idea in a simplified context, the linear model. Four variations of the MINE method for the linear model were created: MINE-like, MINE, MINE with random orthonormal basis, and MINE with random rotation. Each method varies in how it maximizes the MINE criterion. Theorem 1 establishes sufficient conditions for the maximization of the MINE criterion under the linear model. Theorem 2 establishes when the MINE criterion is equivalent to the classic design criterion of D-optimality. By simulation under the linear model, we establish that the MINE with random orthonormal basis and MINE with random rotation are faster to discover the true linear relation with regression coefficients and observations when . We also establish in simulations with , , and 1000 replicates that these two variations of MINE also display a lower false positive rate than the MINE-like method and additionally, for a majority of the experiments, for the MINE method.
机译:进行大规模基因组学实验可能很昂贵,因此实验人员希望从每个实验中获取最多的信息。为此,开发了用于实验设计的“最大信息量的下一个实验(MINE)”标准。在这里,我们在简化的上下文线性模型中探索这个想法。建立了线性模型的MINE方法的四个变体:类MINE,MINE,具有随机正交标准的MINE和具有随机旋转的MINE。每种方法在最大化MINE准则方面各有不同。定理1为线性模型下的MINE准则的最大化建立了充分的条件。定理2确定MINE准则何时等于D优化的经典设计准则。通过在线性模型下进行仿真,我们发现具有正交正交基础的MINE和具有随机旋转的MINE更快地发现了具有回归系数和观测值的真实线性关系。我们还在,,和1000个重复的模拟中确定,这两种MINE变体的假阳性率也比类似MINE的方法低,此外,对于大多数实验而言,对于MINE而言。

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