Analysing matched or paired data

Author(s):  
Janet L. Peacock ◽  
Sally M. Kerry

Chapter 8 covers analysing matched or paired data, and includes the paired t-test, non-normal data, matched case–control data, cohort data, and further reading.

Author(s):  
Janet L. Peacock ◽  
Sally M. Kerry ◽  
Raymond R. Balise

Chapter 8 covers analysing matched or paired data, and includes the paired t test, non-Normal data, matched case-control data, and cohort data. It describes the use of data transformations and how results are interpreted when data are paired. It includes how to calculate 95% confidence intervals for estimates. The chapter includes analyses using Stata, SAS, SPSS, and R.


Biometrics ◽  
2001 ◽  
Vol 57 (4) ◽  
pp. 1106-1112 ◽  
Author(s):  
I-Feng Lin ◽  
Myunghee Cho Paik

2015 ◽  
Vol 26 (3) ◽  
pp. 1323-1340 ◽  
Author(s):  
Beibei Guo ◽  
Ying Yuan

In medical experiments with the objective of testing the equality of two means, data are often partially paired by design or because of missing data. The partially paired data represent a combination of paired and unpaired observations. In this article, we review and compare nine methods for analyzing partially paired data, including the two-sample t-test, paired t-test, corrected z-test, weighted t-test, pooled t-test, optimal pooled t-test, multiple imputation method, mixed model approach, and the test based on a modified maximum likelihood estimate. We compare the performance of these methods through extensive simulation studies that cover a wide range of scenarios with different effect sizes, sample sizes, and correlations between the paired variables, as well as true underlying distributions. The simulation results suggest that when the sample size is moderate, the test based on the modified maximum likelihood estimator is generally superior to the other approaches when the data is normally distributed and the optimal pooled t-test performs the best when the data is not normally distributed, with well-controlled type I error rates and high statistical power; when the sample size is small, the optimal pooled t-test is to be recommended when both variables have missing data and the paired t-test is to be recommended when only one variable has missing data.


Biostatistics ◽  
2000 ◽  
Vol 1 (1) ◽  
pp. 89-105 ◽  
Author(s):  
Peter J. Diggle ◽  
Sara E. Morris ◽  
Jon C. Wakefield

2002 ◽  
Vol 44 (8) ◽  
pp. 936-945 ◽  
Author(s):  
Mikala F. Jarner ◽  
Peter Diggle ◽  
Amanda G. Chetwynd

2019 ◽  
Author(s):  
Nooshin Shomal Zadeh ◽  
Sangdi Lin ◽  
George C Runger

Abstract Motivation Matched case–control analysis is widely used in biomedical studies to identify exposure variables associated with health conditions. The matching is used to improve the efficiency. Existing variable selection methods for matched case–control studies are challenged in high-dimensional settings where interactions among variables are also important. We describe a quite different method for high-dimensional matched case–control data, based on the potential outcome model, which is not only flexible regarding the number of matching and exposure variables but also able to detect interaction effects. Results We present Matched Forest (MF), an algorithm for variable selection in matched case–control data. The method preserves the case and control values in each instance but transforms the matched case–control data with added counterfactuals. A modified variable importance score from a supervised learner is used to detect important variables. The method is conceptually simple and can be applied with widely available software tools. Simulation studies show the effectiveness of MF in identifying important variables. MF is also applied to data from the biomedical domain and its performance is compared with alternative approaches. Availability and implementation R code for implementing MF is available at https://github.com/NooshinSh/Matched_Forest. Supplementary information Supplementary data are available at Bioinformatics online.


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