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本文引用的文献

1
Principles: when there should be no difference--how to fail to reject the null hypothesis.原则:当不应存在差异时——如何未能拒绝原假设。
Trends Pharmacol Sci. 2006 May;27(5):274-8. doi: 10.1016/j.tips.2006.03.006. Epub 2006 Apr 3.

药理学中的良好统计实践。问题2。

Good statistical practice in pharmacology. Problem 2.

作者信息

Lew M

机构信息

Department of Pharmacology, University of Melbourne, The University of Melbourne, Parkville, Victoria, Australia.

出版信息

Br J Pharmacol. 2007 Oct;152(3):299-303. doi: 10.1038/sj.bjp.0707372. Epub 2007 Jul 9.

DOI:10.1038/sj.bjp.0707372
PMID:17618310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2042947/
Abstract

BACKGROUND AND PURPOSE

This paper is intended to assist pharmacologists to make the most of statistical analysis and in avoid common errors.

APPROACH

A scenario is presented where an experimenter performed an experiment to test the effects of two drugs on cultured cells. Analysis of the results, expressed as percentage of control, by a one-way ANOVA yielded P=0.058 and the experimenter concluded that neither drug was effective. The data were expressed as percentage of control because of pairing of the data within each experimental run, a common feature in cell culture experiments. Such data can be analysed with potentially more powerful ANOVA methods equivalent to the paired t-test. Monte Carlo simulations are presented to compare the power of relevant analyses.

RESULTS

For data correlated within experimental run (i.e. paired values), transformation to percentage of control improved the power of a one-way ANOVA to detect a real effect, but a randomized block ANOVA (equivalent to a 2-way ANOVA with experiment and treatment as factors) using the raw values was substantially more powerful. The randomized block ANOVA performed well even with uncorrelated data, being only marginally less powerful than the one-way ANOVA.

CONCLUSIONS AND IMPLICATIONS

A randomized block ANOVA is far superior to the one-way ANOVA with correlated data, and with uncorrelated data it is only marginally less powerful. Thus where there is, or might reasonably be, such a correlation (e.g. relatedness among the data within a single experimental run, or within a multi-well culture plate, or within an animal, et cetera), use the more powerful randomized block ANOVA rather than one-way ANOVA.

摘要

背景与目的

本文旨在帮助药理学家充分利用统计分析并避免常见错误。

方法

给出一个场景,即一位实验者进行了一项实验,以测试两种药物对培养细胞的影响。以对照百分比表示的结果通过单向方差分析得出P = 0.058,实验者得出两种药物均无效的结论。由于每次实验运行中数据的配对,数据以对照百分比表示,这是细胞培养实验中的一个常见特征。此类数据可以用与配对t检验等效的、可能更强大的方差分析方法进行分析。通过蒙特卡罗模拟比较相关分析的效能。

结果

对于实验运行内相关的数据(即配对值),转换为对照百分比提高了单向方差分析检测实际效应的效能,但使用原始值的随机区组方差分析(等同于以实验和处理为因素的双向方差分析)效能要高得多。即使对于不相关的数据,随机区组方差分析也表现良好,其效能仅略低于单向方差分析。

结论与启示

对于相关数据,随机区组方差分析远优于单向方差分析,对于不相关数据,其效能仅略低。因此,在存在或可能合理存在这种相关性的情况下(例如,在单次实验运行内、在多孔培养板内、在动物体内等数据之间的相关性),应使用效能更高的随机区组方差分析而非单向方差分析。