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Testing for bimodality in frequency distributions of data suggesting polymorphisms of drug metabolism--hypothesis testing.

机译:测试数据频率分布中的双峰性表明药物代谢具有多态性-假设测试。

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摘要

1. The theory of methods of hypothesis testing in relation to the detection of bimodality in density distributions is discussed. 2. Practical problems arising from these methods are outlined. 3. The power of three methods of hypothesis testing was compared using simulated data from bimodal distributions with varying separation between components. None of the methods could determine bimodality until the separation between components was 2 standard deviation units and could only do so reliably (greater than 90%) when the separation was as great as 4-6 standard deviation units. 4. The robustness of a parametric and a non-parametric method of hypothesis testing was compared using simulated unimodal distributions known to deviate markedly from normality. Both methods had a high frequency of falsely indicating bimodality with distributions where the components had markedly differing variances. 5. A further test of robustness using power transformation of data from a normal distribution showed that the algorithms could accurately determine unimodality only when the skew of the distribution was in the range 0-1.45.
机译:1.讨论了与密度分布中的双峰检测有关的假设检验方法的理论。 2.概述了由这些方法引起的实际问题。 3.使用来自双峰分布的模拟数据(组件之间具有不同的间隔),比较了三种假设检验方法的功效。在组件之间的间距为2个标准偏差单位之前,没有一种方法可以确定双峰性,并且只有当间距高达4-6个标准偏差单位时,才可以可靠地做到这一点(大于90%)。 4.使用已知明显偏离正态的模拟单峰分布,比较了假设检验和非参数假设检验的鲁棒性。两种方法都有很高的频率错误地指示双峰态,其分布具有明显不同的方差。 5.使用来自正态分布的数据的幂变换对鲁棒性进行的进一步测试表明,仅当分布的偏斜在0-1.45范围内时,算法才能准确确定单峰。

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