株式会社極東書店トップ商品一覧Clinical Trial Data Analysis Using R and SAS. 2nd edition.

商品詳細

Clinical Trial Data Analysis Using R and SAS.

Clinical Trial Data Analysis Using R and SAS. 2nd edition.

・ISBN 978-0-367-73621-7 paper GB£ 54.99

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お気に入り
電子版あり 大学・学術機関向け電子ブック(eBook)ISBN 9781315155104
著者・編者Chen, Ding-Geng (Din) / Peace, Karl E. / Zhang, Pinggao,
シリーズChapman & Hall/CRC Biostatistics Series
出版社(Chapman & Hall/CRC, UK)
出版年月2020
ページ数378 pp.
言語ENG
ニュース番号<M25-833>

解説

Review of the First Edition

"The goal of this book, as stated by the authors, is to fill the knowledge gap that exists between developed statistical methods and the applications of these methods. Overall, this book achieves the goal successfully and does a nice job. I would highly recommend it ...The example-based approach is easy to follow and makes the book a very helpful desktop reference for many biostatistics methods."-Journal of Statistical Software

Clinical Trial Data Analysis Using R and SAS, Second Edition provides a thorough presentation of biostatistical analyses of clinical trial data with step-by-step implementations using R and SAS. The book's practical, detailed approach draws on the authors' 30 years' experience in biostatistical research and clinical development. The authors develop step-by-step analysis code using appropriate R packages and functions and SAS PROCS, which enables readers to gain an understanding of the analysis methods and R and SAS implementation so that they can use these two popular software packages to analyze their own clinical trial data.

What's New in the Second Edition



  • Adds SAS programs along with the R programs for clinical trial data analysis.




  • Updates all the statistical analysis with updated R packages.




  • Includes correlated data analysis with multivariate analysis of variance.




  • Applies R and SAS to clinical trial data from hypertension, duodenal ulcer, beta blockers, familial andenomatous polyposis, and breast cancer trials.




  • Covers the biostatistical aspects of various clinical trials, including treatment comparisons, time-to-event endpoints, longitudinal clinical trials, and bioequivalence trials.