| asyCovTCF {bcROCsurface} | R Documentation |
asyCovTCF computes the asymptotic variance-covariance matrix of full data (FULL) and bias-corrected estimators (i.e. full imputation, mean score imputation, inverse probability weighting, semiparametric efficient and K nearest neighbor) of TCFs.
asyCovTCF(obj_tcf, T, Dvec, V = NULL, rhoEst = NULL, piEst = NULL, BOOT = FALSE, nR = 250, parallel = FALSE, ncpus = ifelse(parallel, detectCores()/2, NULL))
obj_tcf |
a result of a call to |
T |
a numeric vector containing the diagnostic test values. |
Dvec |
a n * 3 binary matrix with three columns, corresponding to the three classes of the disease status. In row i, 1 in column j indicates that the i-th subject belongs to class j, with j = 1, 2, 3. A row of |
V |
a binary vector containing the verification status (1 verified, 0 not verified). |
rhoEst |
a result of a call to |
piEst |
a result of a call to |
BOOT |
a logical value. Default = |
nR |
the number of bootstrap replicates, used when |
parallel |
a logical value. If |
ncpus |
number of processes to be used in parallel computing. Default is half of available cores. |
For bias-corrected estimators of TCFs, the asymptotic variance-covariance matrix at a fixed cut point is estimated by using the Delta method. The function asyCovTCF implements the explicit forms presented in To Duc et al. (2016a, 2016b). In addition, the bootstrap procedure is also available.
For FULL estimator, the asymptotic variance-covariance matrix is computed via bootstrap only.
This function returns an estimated asymptotic variance-covariance matrix for FULL estimator and bias-corrected estimators of TCFs at a fixed cut point.
To Duc, K., Chiogna, M. and Adimari, G. (2016a) Bias-corrected methods for estimating the receiver operating characteristic surface of continuous diagnostic tests. Electronic Journal of Statistics, 10, 3063-3113.
To Duc, K., Chiogna, M. and Adimari, G. (2016b) Nonparametric Estimation of ROC Surfaces Under Verification Bias. https://arxiv.org/abs/1604.04656v1. Submitted.
data(EOC)
# FULL data estimator
Dfull <- preDATA(EOC$D.full, EOC$CA125)
Dvec.full <- Dfull$Dvec
full.tcf <- ROCs.tcf("full", T = EOC$CA125, Dvec = Dvec.full, cps = c(2, 4))
full.var <- asyCovTCF(full.tcf, T = EOC$CA125, Dvec = Dvec.full)
# Preparing the missing disease status
Dna <- preDATA(EOC$D, EOC$CA125)
Dfact.na <- Dna$D
Dvec.na <- Dna$Dvec
rho.out <- rhoMLogit(Dfact.na ~ CA125 + CA153 + Age, data = EOC, test = TRUE)
## FI estimator
fi.tcf <- ROCs.tcf("fi", T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.out, cps = c(2,4))
fi.var <- asyCovTCF(fi.tcf, T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.out)
## MSI estimator
msi.tcf <- ROCs.tcf("msi", T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.out, cps = c(2,4))
msi.var <- asyCovTCF(msi.tcf, T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.out)
## IPW estimator
pi.out <- psglm(V ~ CA125 + CA153 + Age, data = EOC, test = TRUE)
ipw.tcf <- ROCs.tcf("ipw", T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
piEst = pi.out, cps = c(2,4))
ipw.var <- asyCovTCF(ipw.tcf, T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
piEst = pi.out)
## SPE estimator
spe.tcf <- ROCs.tcf("spe", T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.out, piEst = pi.out, cps = c(2,4))
spe.var <- asyCovTCF(spe.tcf, T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.out, piEst = pi.out)
## KNN estimators
XX <- cbind(EOC$CA125, EOC$CA153, EOC$Age)
rho.1nn <- rhoKNN(X = XX, Dvec = Dvec.na, V = EOC$V, K = 1, type = "mahala")
knn.tcf <- ROCs.tcf("knn", T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.1nn, cps = c(2,4))
knn.var <- asyCovTCF(knn.tcf, T = EOC$CA125, Dvec = Dvec.na, V = EOC$V,
rhoEst = rho.1nn)