cROC.kernel {ROCnReg} | R Documentation |
Nonparametric kernel-based estimation of the covariate-specific ROC curve (cROC).
Description
This function estimates the covariate-specific ROC curve (cROC) using the nonparametric kernel-based method proposed by Rodriguez-Alvarez et al. (2011). The method, as it stands now, can only deal with one continuous covariate.
Usage
cROC.kernel(marker, covariate, group, tag.h,
bw = c("LS", "AIC"), regtype = c("LC", "LL"),
data, newdata, pauc = pauccontrol(),
p = seq(0, 1, l = 101), B = 1000, ci.level = 0.95,
parallel = c("no", "multicore", "snow"), ncpus = 1, cl = NULL)
Arguments
marker |
A character string with the name of the diagnostic test variable. |
covariate |
A character string with the name of the continuous covariate. |
group |
A character string with the name of the variable that distinguishes healthy from diseased individuals. |
tag.h |
The value codifying healthy individuals in the variable |
bw |
A character string specifying which method to use to select the bandwidths. AIC specifies expected Kullback-Leibler cross-validation, and LS specifies least-squares cross-validation. Defaults to LS. For details see |
regtype |
A character string specifying which type of kernel estimator to use for the regression function (see Details). LC specifies a local-constant estimator (Nadaraya-Watson) and LL specifies a local-linear estimator. Defaults to LC. For details see |
data |
Data frame representing the data and containing all needed variables. |
newdata |
Optional data frame containing the values of the covariates at which the covariate-specific ROC curve (AUC and pAUC, if computed) will be computed. If not supplied, the function |
pauc |
A list of control values to replace the default values returned by the function |
p |
Set of false positive fractions (FPF) at which to estimate the covariate-specific ROC curve. This set is also used to compute the area under the covariate-specific ROC curve using Simpson's rule. Thus, the length of the set should be an odd number, and it should be rich enough for an accurate estimation. |
B |
An integer value specifying the number of bootstrap resamples for the construction of the confidence intervals. The default is 1000. |
ci.level |
An integer value (between 0 and 1) specifying the confidence level. The default is 0.95. |
parallel |
A characters string with the type of parallel operation: either "no" (default), "multicore" (not available on Windows) or "snow". |
ncpus |
An integer with the number of processes to be used in parallel operation. Defaults to 1. |
cl |
An object inheriting from class |
Details
Estimates the covariate-specific ROC curve (cROC) defined as
ROC(p|x) = 1 - F_{D}\{F_{\bar{D}}^{-1}(1-p|x)|x\},
where
F_{D}(y|x) = Pr(Y_{D} \leq y | X_{D} = x ),
F_{\bar{D}}(y|x) = Pr(Y_{\bar{D}} \leq y | X_{\bar{D}} = x).
Note that, for the sake of clarity, we assume that the covariate of interest is the same in both healthy and diseased populations. In particular, the method implemented in this function estimates F_{D}(\cdot|x)
and F_{\bar{D}}(\cdot|x)
assuming a nonparametric location-scale regression model for Y
in each population separately, i.e.,
Y_{D} = \mu_{D}(X_{D}) + \sigma_{D}(X_{D})\varepsilon_{D},
Y_{\bar{D}} = \mu_{\bar{D}}(X_{\bar{D}}) + \sigma_{\bar{D}}(X_{\bar{D}})\varepsilon_{\bar{D}},
where \mu_{D}(x) = E(Y_D | X_D = x)
, \mu_{\bar{D}}(x) = E(Y_{\bar{D}} | X_{\bar{D}} = x)
(regression function), \sigma^2_{D}(x) = Var(Y_D | X_D = x)
, \sigma^2_{\bar{D}}(x) = Var(Y_{\bar{D}} | X_{\bar{D}} = x)
(variance functions), and \varepsilon_{D}
and \varepsilon_{\bar{D}}
have zero mean, variance one, and distribution functions G_{D}
and G_{\bar{D}}
, respectively. In this case, the covariate-specific ROC curve can be expressed as
ROC(p|x) = 1 - G_{D}\{a(\mathbf{x}) + b(\mathbf{x})G_{\bar{D}}^{-1}(1-p)\},
where a(x) = \frac{\mu_{\bar{D}}(x) - \mu_{D}(x)}{\sigma_{D}(x)}
, b(x) = \frac{\sigma_{\bar{D}}(x)}{\sigma_{D}(x)}
, and G_{D}
and G_{\bar{D}}
are the distribution functions of \varepsilon_{D}
and \varepsilon_{\bar{D}}
, respectively.
By default, for both the healthy and diseased population, both the regression and variance functions are estimated using the Nadaraya-Watson estimator (LC), and the bandwidth are selected using least-squares cross-validation (LS). Implementation relies on the R
-package np
. No assumptions are made about G_{D}
and G_{\bar{D}}
, which are empirically estimated on the basis of standardised residuals.
The covariate-specific area under the curve is
AUC(\mathbf{x})=\int_{0}^{1}ROC(p|\mathbf{x})dp,
and is computed numerically (using Simpson's rule). With regard to the partial area under the curve, when focus = "FPF"
and assuming an upper bound u_1
for the FPF, what it is computed is
pAUC_{FPF}(u_1|\mathbf{x})=\int_0^{u_1} ROC(p|\mathbf{x})dp,
where again the integral is approximated numerically (Simpson's rule). The returned value is the normalised pAUC, pAUC_{FPF}(u_1|\mathbf{x})/u_1
so that it ranges from u_1/2
(useless test) to 1 (perfect marker). Conversely, when focus = "TPF"
, and assuming a lower bound for the TPF of u_2
, the partial area corresponding to TPFs lying in the interval (u_2,1)
is computed as
pAUC_{TPF}(u_2|\mathbf{x})=\int_{u_2}^{1}ROC_{TNF}(p|\mathbf{x})dp,
where ROC_{TNF}(p|\mathbf{x})
is a 270^\circ
rotation of the ROC curve, and it can be expressed as ROC_{TNF}(p|\mathbf{x}) = F_{\bar{D}}\{F_{D}^{-1}(1-p|\mathbf{x})|\mathbf{x}\}=G_{\bar{D}}\{\frac{\mu_{D}(x)-\mu_{\bar{D}}(x)}{\sigma_{\bar{D}}(x)}+G_{D}^{-1}(1-p)\frac{\sigma_{D}(x)}{\sigma_{\bar{D}}(x)}\}.
Again, the computation of the integral is done via Simpson's rule. The returned value is the normalised pAUC, pAUC_{TPF}(u_2|\mathbf{x})/(1-u_2)
, so that it ranges from (1-u_2)/2
(useless test) to 1 (perfect test).
Value
As a result, the function provides a list with the following components:
call |
The matched call. |
newdata |
A data frame containing the values of the covariates at which the covariate-specific ROC curve (AUC and pAUC, if required) was computed. |
data |
The original supplied data argument. |
missing.ind |
A logical value indicating whether for each pair of observations (test outcomes and covariates) missing values occur. |
marker |
The name of the diagnostic test variable in the dataframe. |
group |
The value of the argument |
tag.h |
The value of the argument |
covariate |
The value of the argument |
p |
Set of false positive fractions (FPF) at which the covariate-specific ROC curve has been estimated. |
ci.level |
The value of the argument |
ROC |
Estimated covariate-specific ROC curve (AROC), and |
AUC |
Estimated area under the covariate-specific ROC curve, and |
pAUC |
If computed, estimated partial area under the covariate-adjusted ROC curve and |
fit |
Named list of length two, with components 'h' (healthy) and 'd' (diseased). Each component of the list contains the following information: (1) |
References
Hayfield, T., and Racine, J. S.(2008). Nonparametric Econometrics: The np Package. Journal of Statistical Software 27(5). URL http://www.jstatsoft.org/v27/i05/.
Rodriguez-Alvarez, M. X., Roca-Pardinas, J., and Cadarso-Suarez, C. (2011). ROC curve and covariates: extending induced methodology to the non-parametric framework. Statistics and Computing, 21, 483–499.
See Also
AROC.bnp
, AROC.sp
, AROC.kernel
, pooledROC.BB
, pooledROC.emp
, pooledROC.kernel
, pooledROC.dpm
, cROC.kernel
or cROC.sp
.
Examples
library(ROCnReg)
data(psa)
# Select the last measurement
newpsa <- psa[!duplicated(psa$id, fromLast = TRUE),]
# Log-transform the biomarker
newpsa$l_marker1 <- log(newpsa$marker1)
cROC_kernel <- cROC.kernel(marker = "l_marker1",
covariate = "age",
group = "status",
tag.h = 0,
data = newpsa,
bw = "LS",
regtype = "LC",
p = seq(0, 1, len = 101),
pauc = pauccontrol(compute = TRUE, value = 0.5, focus = "FPF"),
B = 500)
plot(cROC_kernel)
summary(cROC_kernel )