Description Usage Arguments Details Value Author(s) References See Also Examples
This function is to calculate composite scores of a multi-marker molecular signature based on an interaction model.
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time |
A numeric vector containing the follow up time for right censored data. |
event |
A numeric vector containing the status indicator, normally 0=alive, 1=dead. |
treat |
A numeric vector containing the treatment indicator: 1=treatment of interest, 0=alternative treatment (e.g. placebo or standard of care). |
bio |
A numeric data frame or matrix containing biomarker values. |
covar |
A numeric matrix containing clinical covariates. Default is |
nfolds |
The number of folds for cross validation in choosing tuning parameters. The function |
alpha |
A scalar for the elasticnet mixing parameter as in the “glmnet” package (0=ridge, 1=lasso). A fixed value is supposed to be used, without searching for the optimal alpha value. Default is 0.5. |
pos.direction |
A logical value indicating whether a subgroup with hazard ratio > 1 is desirable. Default is |
This function is a function called by MMMS()
to calculate MMMS composite scores. An interaction model is considered by assuming that a treatment-specific subgroup exists. The composite scores based on interaction terms and main-effect terms are both calculated via elastic net as implemented by the “glmnet” package. The composite scores based on interaction terms are used for identifying treatment-specific subgroups, while those based on main-effect terms are used for adjusting for biomarker main effect.
A list with the following elements:
score |
The composite scores based interaction terms for the treatment arm of interest ( |
score.all |
The composite scores based on interaction terms for all patients. |
score.main |
The composite scores based on main-effect terms. |
coefs |
Elnet coefficient estimates for interaction terms. |
coefs.main |
Elnet coefficient estimates for main-effect terms. |
fit |
The |
lam.best |
The optimal |
treat |
The treatment variable in the input data. |
alpha |
The |
Author: Lin Li, Tobias Guennel,Scott Marshall, Leo Wang-Kit Cheung
Contributors: Brigid M. Wilson, Dilan C. Paranagama
Maintainer: Lin Li <lli@biostatsolutions.com>
Lin Li, Tobias Guennel, Scott Marshall, Leo Wang-Kit Cheung (2014) A multi-marker molecular signature approach for treatment-specific subgroup identification with survival outcomes. The Pharmacogenomics Journal. http://dx.doi.org/10.1038/tpj.2014.9
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