Clinical trial data analysis with R and SAS.
Material type:
TextLanguage: English Series: Chapman & Hall/CRC biostatistics seriesPublication details: Chapman & Hall, 2017.Edition: Second edition; Ding-Geng (Din) Chen, Karl E. Peace, Pinggao ZhangDescription: xxxii, 378 pages : illustrations ; 24 cmISBN: - 9781498779524 (hardback : alk. paper)
- 1498779522 (hardback : alk. paper)
- Clinical trial data analysis using R
- 610.727 23 CHE
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CUTN Central Library Medicine, Technology & Management | Non-fiction | 610.727 CHE (Browse shelf(Opens below)) | Available | 52024 |
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| 610.724 CHO Adaptive design methods in clinical trials | 610.724 MUN. Nutrition Assessment: Clinical and Research Applications: Clinical and Research Applications / | 610.724 RAB Biomarker Analysis in Clinical Trials with R / | 610.727 CHE Clinical trial data analysis with R and SAS. | 610.727 COL Modelling survival data in medical research / | 610.727 LEG Advanced survival models [electronic resource] / | 610.73 AGA Anatomy physiology and health education / |
"Major updates to include SAS programs"--Preface.
Previous edition: Clinical trial data analysis using R / Ding-Geng Chen, Karl E. Peace (Boca Raton, Florida : CRC Press, 2011).
Includes bibliographical references (pages 363-371) and index.
Preface.
Introduction to R.
Overview of Clinical Trials.
Sample Size Determination in Clinical Trials.
Two Treatment Comparisons in Clinical Trials.
Multi-Arm Comparisons in Clinical Trials (ANOVA).
Treatment Comparisons Incorporating Covariates in Clinical Trials (ANCOVA).
Clinical Trials with Time-to-Events Endpoints.
Clinical Trials with Repeated Measures.
Meta-Analysis in Clinical Trials.
Bayesian Methods in Clinical Trials.
Group Sequential Designs and Monitoring in Clinical Trials.
Bioequivalence Clinical Trials.
Monitoring Clinical Trials for Adverse Events.
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.
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