coxpls3DR | R Documentation |
This function computes the PLSR model with the Residuals of a Cox-Model
fitted with an intercept as the only explanatory variable as the response
and Xplan as explanatory variables. Default behaviour uses the Deviance
residuals. It uses the package plsRglm
.
coxpls3DR(Xplan, ...) ## Default S3 method: coxpls3DR( Xplan, time, time2, event, type, origin, typeres = "deviance", collapse, weighted, scaleX = TRUE, scaleY = TRUE, nt = min(7, ncol(Xplan)), typeVC = "none", plot = FALSE, allres = FALSE, sparse = FALSE, sparseStop = TRUE, ... ) ## S3 method for class 'formula' coxpls3DR( Xplan, time, time2, event, type, origin, typeres = "deviance", collapse, weighted, scaleX = TRUE, scaleY = TRUE, nt = min(7, ncol(Xplan)), typeVC = "none", plot = FALSE, allres = FALSE, dataXplan = NULL, subset, weights, model_frame = FALSE, sparse = FALSE, sparseStop = TRUE, model_matrix = FALSE, contrasts.arg = NULL, ... )
Xplan |
a formula or a matrix with the eXplanatory variables (training) dataset |
... |
Arguments to be passed on to |
time |
for right censored data, this is the follow up time. For interval data, the first argument is the starting time for the interval. |
time2 |
The status indicator, normally 0=alive, 1=dead. Other choices
are |
event |
ending time of the interval for interval censored or counting
process data only. Intervals are assumed to be open on the left and closed
on the right, |
type |
character string specifying the type of censoring. Possible
values are |
origin |
for counting process data, the hazard function origin. This option was intended to be used in conjunction with a model containing time dependent strata in order to align the subjects properly when they cross over from one strata to another, but it has rarely proven useful. |
typeres |
character string indicating the type of residual desired.
Possible values are |
collapse |
vector indicating which rows to collapse (sum) over. In
time-dependent models more than one row data can pertain to a single
individual. If there were 4 individuals represented by 3, 1, 2 and 4 rows of
data respectively, then |
weighted |
if |
scaleX |
Should the |
scaleY |
Should the |
nt |
Number of PLSR components to fit. |
typeVC |
type of leave one out crossed validation. Several procedures are available and may be forced.
|
plot |
Should the survival function be plotted ?) |
allres |
FALSE to return only the Cox model and TRUE for additionnal results. See details. Defaults to FALSE. |
sparse |
should the coefficients of non-significant predictors
(< |
sparseStop |
should component extraction stop when no significant
predictors (< |
dataXplan |
an optional data frame, list or environment (or object
coercible by |
subset |
an optional vector specifying a subset of observations to be used in the fitting process. |
weights |
an optional vector of 'prior weights' to be used in the
fitting process. Should be |
model_frame |
If |
model_matrix |
If |
contrasts.arg |
a list, whose entries are values (numeric matrices, functions or character strings naming functions) to be used as replacement values for the contrasts replacement function and whose names are the names of columns of data containing factors. |
If allres=FALSE
returns only the final Cox-model. If
allres=TRUE
returns a list with the PLS components, the final
Cox-model and the PLSR model. allres=TRUE
is useful for evluating
model prediction accuracy on a test sample.
If allres=FALSE
:
cox_pls3DR |
Final Cox-model. |
If
allres=TRUE
:
tt_pls3DR |
PLSR components. |
cox_pls3DR |
Final Cox-model. |
pls3DR_mod |
The PLSR model. |
Frédéric Bertrand
frederic.bertrand@utt.fr
http://www-irma.u-strasbg.fr/~fbertran/
plsRcox, Cox-Models in a high dimensional setting in R, Frederic
Bertrand, Philippe Bastien, Nicolas Meyer and Myriam Maumy-Bertrand (2014).
Proceedings of User2014!, Los Angeles, page 152.
Deviance residuals-based sparse PLS and sparse kernel PLS regression for censored data, Philippe Bastien, Frederic Bertrand, Nicolas Meyer and Myriam Maumy-Bertrand (2015), Bioinformatics, 31(3):397-404, doi:10.1093/bioinformatics/btu660.
coxph
, PLS_lm
data(micro.censure) data(Xmicro.censure_compl_imp) X_train_micro <- apply((as.matrix(Xmicro.censure_compl_imp)),FUN="as.numeric",MARGIN=2)[1:80,] X_train_micro_df <- data.frame(X_train_micro) Y_train_micro <- micro.censure$survyear[1:80] C_train_micro <- micro.censure$DC[1:80] (cox_pls3DR_fit <- coxpls3DR(X_train_micro,Y_train_micro,C_train_micro,nt=7)) (cox_pls3DR_fit2 <- coxpls3DR(~X_train_micro,Y_train_micro,C_train_micro,nt=7)) (cox_pls3DR_fit3 <- coxpls3DR(~.,Y_train_micro,C_train_micro,nt=7,dataXplan=X_train_micro_df)) (cox_pls3DR_fit4 <- coxpls3DR(~.,Y_train_micro,C_train_micro,nt=7,typeVC="none", data=X_train_micro_df,sparse=TRUE)) (cox_pls3DR_fit5 <- coxpls3DR(~.,Y_train_micro,C_train_micro,nt=7,typeVC="none", data=X_train_micro_df,sparse=TRUE,sparseStop=FALSE)) rm(X_train_micro,Y_train_micro,C_train_micro,cox_pls3DR_fit,cox_pls3DR_fit2, cox_pls3DR_fit3,cox_pls3DR_fit4,cox_pls3DR_fit5)
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