Changes in version 0.3.3 Fixes a bug when using step1 = "lasso" where columns were being subset incorrectly when creating the design matrix for glmnet::cv.glmnet. Fixes a bug when using step1 = "lasso" where factor variables were treated as numeric. Factors are appropriately now converted into indicator variables. Changes in version 0.3.2 Minor documentation updates following JOSS publication. Changes in version 0.3.1 Release corresponding to JOSS paper. Adds automated testing for Step 1 wrapper functions (e.g., vt1_lasso) and get_mnpp. Changes in version 0.3.0 (2023-04-01) Adds support for classification trees in Step 2 by setting step2 = 'classtree' with a given threshold of threshold. Adds the print.tunevt method. Changes in version 0.2.1 Fixes a bug where zbar was calculated using the mean difference in the first column of the data instead of using the location of the variable Y. Changes in version 0.2.0 Adds the parallel option to tunevt to support parallel backends. Changes in version 0.1.1 (2022-11-07) This patch reconciles an invalid URI in the tunevt documentation's references. Changes in version 0.1.0 This is a new package that implements the Virtual Twins algorithm for subgroup identification (Foster et al., 2011) while controlling the probability of falsely detecting differential treatment effects when the conditional treatment effect is constant across the population of interest. These methods were originally presented in Wolf et al. (2022). References - Foster, J. C., Taylor, J. M., & Ruberg, S. J. (2011). Subgroup identification from randomized clinical trial data. Statistics in Medicine, 30(24), 2867–2880. https://doi.org/10.1002/sim.4322 - Wolf, J. M., Koopmeiners, J. S., & Vock, D. M. (2022). A permutation procedure to detect heterogeneous treatment effects in randomized clinical trials while controlling the type-I error rate. Clinical Trials. https://doi.org/10.1177/17407745221095855 Key function - tunevt() fits a Virtual Twins model using user-specified Step 1 and Step 2 models with parameter selection to control the probability of a false discovery.