Regression and ANOVA: An Integrated Approach Using SAS Software

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SAS Institute, May 1, 2002 - Computers - 578 pages
This book provides a thorough and integrated treatment of multiple regression and ANOVA. The information it contains has served as the basis for a graduate-level biostatistics class at the University of North Carolina at Chapel Hill. The book focuses on the general linear model (GLM) theory, stated in matrix terms, which provides a more compact, clear, and unified presentation of regression and ANOVA than do traditional sums of squares and scalar equations. The book offers a balanced treatment of regression and ANOVA, yet is very compact. Reflecting current computational practice, most sums of squares formulas and associated theory, especially in ANOVA, are not included. The text includes almost no proofs, despite the presence of a large number of basic theoretical results. Many numerical examples are provided and include both the SAS code and equivalent mathematical representation needed to produce the outputs that are presented. All exercises involve only real data, collected in the course of scientific research. The book is divided into sections covering the following topics: basic theory; multiple regression; model building and evaluation; ANOVA; and ANCOVA.

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About the author (2002)

Keith E. Muller, Ph.D., is Associate Professor of Biostatistics at the University of North Carolina at Chapel Hill. He teaches classes and seminars on the theory and practice of univariate and multivariate linear models with Gaussian errors. A SAS user since 1978, he is best known for his contributions to theory and practice of sample size and power calculations, including IML programs for power in repeated measures.

Bethel A. Fetterman, M.S., is Director of Clinical Data Processing and Analysis at PharmaLinkFHI in Research Triangle Park, North Carolina. She is currently on leave from the doctoral program in Biostatistics at the University of North Carolina at Chapel Hill. A SAS user since 1989, she uses SAS software in designing, managing, analyzing, and reporting clinical trials of new pharmaceuticals.

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