Sample individual casual treatment effects from given D-vine copula model in binary continuous setting
sample_deltas_BinCont(
copula_par,
rotation_par,
copula_family1,
copula_family2 = copula_family1,
n,
q_S0 = NULL,
q_S1 = NULL,
q_T0 = NULL,
q_T1 = NULL,
marginal_sp_rho = TRUE,
setting = "BinCont",
composite = FALSE,
plot_deltas = FALSE,
restr_time = +Inf
)
A list with two elements:
Delta_dataframe
: a dataframe containing the sampled individual causal
treatment effects
marginal_sp_rho_matrix
: a matrix containing the marginal pairwise Spearman's rho
parameters estimated from the sample. If marginal_sp_rho = FALSE
, this
matrix is not computed and NULL
is returned for this element of the list.
Parameter vector for the sequence of bivariate copulas that
define the D-vine copula. The elements of copula_par
correspond to
\((c_{12}, c_{23}, c_{34}, c_{13;2}, c_{24;3}, c_{14;23})\).
Vector of rotation parameters for the sequence of
bivariate copulas that define the D-vine copula. The elements of
rotation_par
correspond to \((c_{12}, c_{23}, c_{34}, c_{13;2},
c_{24;3}, c_{14;23})\).
Copula family of \(c_{12}\) and \(c_{34}\). For the
possible options, see loglik_copula_scale()
. The elements of
copula_family
correspond to \((c_{12}, c_{34})\).
Copula family of the other bivariate copulas. For the
possible options, see loglik_copula_scale()
. The elements of
copula_family2
correspond to \((c_{23}, c_{13;2}, c_{24;3}, c_{14;23})\).
Number of samples to be taken from the D-vine copula.
Quantile function for the distribution of \(S_0\).
Quantile function for the distribution of \(S_1\).
Quantile function for the distribution of \(T_0\). This should be
NULL
if \(T_0\) is binary.
Quantile function for the distribution of \(T_1\). This should be
NULL
if \(T_1\) is binary.
(boolean) Compute the sample Spearman correlation
matrix? Defaults to TRUE
.
Should be one of the following two:
"BinCont"
: for when \(S\) is continuous and \(T\) is binary.
"SurvSurv"
: for when both \(S\) and \(T\) are time-to-event variables.
(boolean) If composite
is TRUE
, then the surrogate
endpoint is a composite of both a "pure" surrogate endpoint and the true
endpoint, e.g., progression-free survival is the minimum of time-to-progression
and time-to-death.
Plot the sampled individual causal effects? Defaults to
FALSE
.
Restriction time for the potential outcomes. Defaults to
+Inf
which means no restriction. Otherwise, the sampled potential outcomes
are replace by pmin(S0, restr_time)
(and similarly for the other potential
outcomes).