Comparison of Several Treatments with a Control Using Multiple Contrasts
用多重对比比较若干处理与对照AI 解读 ↓
本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。
DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。
引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。
关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。
AI 根据所提供的论文材料归类:摘要讨论受限备择下的实验多重比较,未明确涉及因果识别方法或其他所列细分。
反馈分类问题用多重对比比较若干处理与对照AI 解读 ↓
正在核对关联版本…
正在核对对应版本的资源…
A problem frequently encountered in the practice of statistics is the comparison of several treatments with a control or standard. We consider an experimental situation where prior knowledge indicates that all of the treatments are at least as effective as the control and the problem is to determine if any are significantly better than the control. A number of statistical procedures have been proposed for this situation, of which the best known is Dunnett's (1955) multiple comparison procedure. Dunnett's test rejects equality of the treatments and the control for a large value of the maximum contrast of the data vector with several vectors that are located “symmetrically” within the alternative region. We study a large class of such tests, which includes Dunnett's test as a particular case. One of these tests, which is based on the maximum contrast of the data vector with several orthogonal vectors, is very easy to implement and has an uncomplicated, good, and fairly uniform power function over the entire alternative region. In fact, a small Monte Carlo power study suggests that this orthogonal contrast test is approximately “maximin” within this class of tests. Moreover, the simplicity of the power function of the orthogonal contrast test enables the experimenter to determine sample sizes for designed experiments with specific power characteristics. Such sample size determinations can be difficult, if not impossible, using other procedures. Abelson and Tukey (1963) suggested tests for a large class of restricted problems that are based on contrasts of the data vector with a single vector that is “centrally” located within the alternative region. These single contrast tests have the advantage that their distributions under the null hypotheses (a t distribution) and under the alternative (a noncentral t distribution) are rather simple. For the problem studied in this article the Abelson–Tukey contrast test is also a member of the class of tests proposed. Its power function varies considerably over the alternative region, with a high power in the center but very low power near the boundaries of the alternative region. The power of Dunnett's test has similar characteristics with less pronounced extremes. If only one of the treatments is effective, then a single contrast with the appropriate “corner” of the alternative region would have highest power. Of course, such a test would require prior knowledge of which treatment might be effective. Such a single contrast test is not in the class of tests studied here. Within this class of tests, the most powerful test when only one treatment is effective is based on the maximum contrast with all of the corners of the alternative region. Such a test has low power in a “center” of the alternative, that is, if all of the treatments are equally effective. Each test in the class of tests proposed here is associated with a set of vectors that are “strategically” located within the alternative region. The particular “strategy” chosen would depend on which alternatives are most important to protect against. Each such set of vectors can be regarded as a convex combination of the corner vectors of the alternative and the center vector. This center vector corresponds to the single contrast of Abelson and Tukey. The choice of the particular convex combination depends on the experimenter's belief regarding the relative magnitudes of the “common” effectiveness of the treatments and their individual effectiveness. If, for example, in a drug experiment each treatment is a combination of a common drug, known to be effective, and some individual new drug, the experimenter may wish to determine the convex combination based on his belief of the relative effectiveness of the new drugs. In the absence of such prior information we recommend the orthogonal contrast test for its simplicity and uniform power.