The hardware and bandwidth for this mirror is donated by dogado GmbH, the Webhosting and Full Service-Cloud Provider. Check out our Wordpress Tutorial.
If you wish to report a bug, or if you are interested in having us mirror your free-software or open-source project, please feel free to contact us at mirror[@]dogado.de.
Bootstrap confidence intervals depend on three elements:
The first two of these depend only on the bootstrap distribution, and not how it is generated: parametrically or non-parametrically.
Package bcaboot
aims to make construction of bootstrap confidence intervals almost automatic. The three main functions for the user are:
bcajack
and bcajack2
for nonparametric bootstrapbcapar
for parametric bootstrapFurther details are in the Efron and Narasimhan (2018) paper. Much of the theory behind the approach can be found in references Efron (1987), T. DiCiccio and Efron (1992), T. J. DiCiccio and Efron (1996), and Efron and Hastie (2016).
Suppose we wish to construct bootstrap confidence intervals for an \(R^2\)-statistic from a linear regression. Using the diabetes data from the lars
(442 by 11) as an example, we use the function below to regress the y
on x
, a matrix of of 10 predictors, to compute \(R^2\).
data(diabetes, package = "bcaboot")
Xy <- cbind(diabetes$x, diabetes$y)
rfun <- function(Xy) {
y <- Xy[, 11]
X <- Xy[, 1:10]
summary(lm(y ~ X) )$adj.r.squared
}
Constructing bootstrap confidence intervals involves merely calling bcajack
:
set.seed(1234)
result <- bcajack(x = Xy, B = 2000, func = rfun, verbose = FALSE)
The result
contains several components. The confidence interval limits can be obtained via
knitr::kable(result$lims, digits = 3)
bca | jacksd | std | pct | |
---|---|---|---|---|
0.025 | 0.435 | 0.003 | 0.443 | 0.006 |
0.05 | 0.443 | 0.006 | 0.453 | 0.015 |
0.1 | 0.454 | 0.001 | 0.465 | 0.035 |
0.16 | 0.464 | 0.002 | 0.474 | 0.065 |
0.5 | 0.498 | 0.001 | 0.507 | 0.306 |
0.84 | 0.531 | 0.002 | 0.539 | 0.685 |
0.9 | 0.540 | 0.002 | 0.548 | 0.778 |
0.95 | 0.551 | 0.002 | 0.560 | 0.869 |
0.975 | 0.560 | 0.002 | 0.570 | 0.923 |
The first column shows the estimated Bca confidence limits at the requested alpha percentiles which can be compared with the standard limits \(\theta \pm \hat{\sigma}z_{\alpha}\) under the column titled standard
. The jacksd
column jacksd gives the internal standard errors for the Bca limits, quite small in this example. The pct
column gives percentiles of the ordered B
bootstrap replications corresponding to the Bca limits, e.g. the 91.85 percentile equals the the .975 Bca limit .5600968.
Further details are provided by the stats
component.
knitr::kable(result$stats, digits = 3)
theta | sdboot | z0 | a | sdjack | |
---|---|---|---|---|---|
est | 0.507 | 0.032 | -0.253 | -0.007 | 0.033 |
jsd | 0.000 | 0.001 | 0.031 | 0.000 | 0.000 |
The first column theta
is the original point estimate of the parameter of interest, sdboot
is its bootstrap estimate of standard error. The quantity z0
is the Bca bias correction value, in this case quite negative; a
is the acceleration, a component of the Bca limits (nearly zero here). Finally, sdjack
is the jackknife estimate of standard error for theta
.
The bottom line gives the internal standard errors for the five quantities above. This is substantial for z0
above.
The component ustats
of the result provides the bias-corrected estimator and an estimate of its sampling error.
knitr::kable(t(result$ustats), digits = 3)
ustat | sdu |
---|---|
0.498 | 0.036 |
The resulting object can be plotted using bcaplot
.
bcaplot(result)
A logistic regression was fit to data on 812 neonates at a large clinic. Here is a summary of the dataset.
str(neonates)
## 'data.frame': 812 obs. of 12 variables:
## $ gest: num -0.729 -0.729 1.156 -2.884 0.348 ...
## $ ap : num 0.856 0.856 0.856 -2.076 0.856 ...
## $ bwei: num -0.694 -0.694 0.786 -2.174 0.786 ...
## $ gen : num 1.227 -0.814 -0.814 1.227 -0.814 ...
## $ resp: num 0.78 -0.939 1.639 1.639 1.639 ...
## $ head: num -0.402 -0.402 -0.402 -0.402 -0.402 ...
## $ hr : num -0.256 -0.256 -0.256 -0.256 -0.256 ...
## $ cpap: num 1.866 -0.535 1.866 1.866 1.866 ...
## $ age : num -0.94 -0.94 -0.94 -0.94 1.06 ...
## $ temp: num -0.669 -0.669 -0.669 -0.669 2.339 ...
## $ size: num 0.484 -1.319 -1.319 0.484 0.484 ...
## $ y : int 1 1 1 1 1 1 1 1 1 1 ...
The goal was to predict death versus survival—\(y\) is 1 or 0, respectively—on the basis of 11 baseline variables of which one of them resp
was of particular concern. (There were 207 deaths and 605 survivors.) So here \(\theta\), the parameter of interest is the coefficient of resp
. Discussions with the investigator suggested a weighting of 4 to 1 of deaths versus non-deaths.
weights <- with(neonates, ifelse(y == 0, 1, 4))
glm_model <- glm(formula = y ~ ., family = "binomial", weights = weights, data = neonates)
summary(glm_model)
##
## Call:
## glm(formula = y ~ ., family = "binomial", data = neonates, weights = weights)
##
## Deviance Residuals:
## Min 1Q Median 3Q Max
## -3.0338 -0.9211 -0.5607 0.1697 3.9021
##
## Coefficients:
## Estimate Std. Error z value Pr(>|z|)
## (Intercept) -0.26510 0.07598 -3.489 0.000485 ***
## gest -0.70602 0.13117 -5.383 7.35e-08 ***
## ap -0.78594 0.07874 -9.982 < 2e-16 ***
## bwei -0.23332 0.12592 -1.853 0.063879 .
## gen -0.04107 0.07355 -0.558 0.576594
## resp 0.94306 0.08974 10.509 < 2e-16 ***
## head 0.04813 0.08057 0.597 0.550299
## hr 0.03504 0.07191 0.487 0.626045
## cpap 0.43438 0.08869 4.898 9.70e-07 ***
## age 0.15727 0.08492 1.852 0.064041 .
## temp -0.05960 0.08506 -0.701 0.483520
## size -0.37477 0.09919 -3.778 0.000158 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## (Dispersion parameter for binomial family taken to be 1)
##
## Null deviance: 1951.7 on 811 degrees of freedom
## Residual deviance: 1187.2 on 800 degrees of freedom
## AIC: 1211.2
##
## Number of Fisher Scoring iterations: 5
Parametric bootstrapping in this context requires us to independently sample the response according to the estimated probabilities from regression model. As discussed in the paper accompanying this software, routine bcapar
also requires sufficient statistics \(\hat{\beta} = M^\prime y\) where \(M\) is the model matrix. Therefore, it makes sense to have a function do the work. The function glm_boot
below returns a list of the estimate \(\hat{\theta}\), the bootstrap estimates, and the sufficient statistics.
glm_boot <- function(B, glm_model, weights, var = "resp") {
pi_hat <- glm_model$fitted.values
n <- length(pi_hat)
y_star <- sapply(seq_len(B), function(i) ifelse(runif(n) <= pi_hat, 1, 0))
beta_star <- apply(y_star, 2, function(y) {
boot_data <- glm_model$data
boot_data$y <- y
coef(glm(formula = y ~ ., data = boot_data, weights = weights, family = "binomial"))
})
list(theta = coef(glm_model)[var],
theta_star = beta_star[var, ],
suff_stat = t(y_star) %*% model.matrix(glm_model))
}
Now we can compute the bootstrap estimates using bcapar
.
set.seed(3891)
glm_boot_out <- glm_boot(B = 2000, glm_model = glm_model, weights = weights)
glm_bca <- bcapar(t0 = glm_boot_out$theta,
tt = glm_boot_out$theta_star,
bb = glm_boot_out$suff_stat)
We can examine the bootstrap limits and statistics.
knitr::kable(glm_bca$lims, digits = 3)
bca | jacksd | pct | std | |
---|---|---|---|---|
0.025 | 0.598 | 0.025 | 0.006 | 0.639 |
0.05 | 0.655 | 0.019 | 0.016 | 0.688 |
0.1 | 0.717 | 0.011 | 0.040 | 0.745 |
0.16 | 0.764 | 0.007 | 0.073 | 0.789 |
0.5 | 0.913 | 0.004 | 0.333 | 0.943 |
0.84 | 1.067 | 0.005 | 0.710 | 1.097 |
0.9 | 1.114 | 0.009 | 0.797 | 1.142 |
0.95 | 1.168 | 0.008 | 0.880 | 1.198 |
0.975 | 1.214 | 0.013 | 0.930 | 1.247 |
knitr::kable(glm_bca$stats, digits = 3)
theta | sd | a | az | z0 | A | sdd | mean | |
---|---|---|---|---|---|---|---|---|
est | 0.943 | 0.155 | -0.019 | -0.001 | -0.215 | 0.006 | 0.129 | 0.982 |
jsd | 0.000 | 0.002 | 0.007 | 0.010 | 0.027 | 0.025 | 0.005 | 0.004 |
Our bootstrap standard error using \(B=2000\) samples for resp
can be read off from the last table as \(0.943\pm 0.155\). We can also see a small upward bias from the fact that 0.585 proportion of bootstrap replicates were above \(0.943\). This is also reflected in the bias-corrector term \(\hat{z}_0= -0.215\) in the table above with an internal standard error of $0.024.
Now suppose we wish to use a nonstandard estimation procedure, for example, via the glmnet
package, which uses cross-validation to figure out a best fit, corresponding to a penalization parameter \(\lambda\) (named lambda.min
).
X <- as.matrix(neonates[, seq_len(11)]) ; Y <- neonates$y;
glmnet_model <- glmnet::cv.glmnet(x = X, y = Y, family = "binomial", weights = weights)
We can examine the estimates at the lambda.min
as follows.
coefs <- as.matrix(coef(glmnet_model, s = glmnet_model$lambda.min))
knitr::kable(data.frame(variable = rownames(coefs), coefficient = coefs[, 1]), row.names = FALSE, digits = 3)
variable | coefficient |
---|---|
(Intercept) | -0.212 |
gest | -0.540 |
ap | -0.687 |
bwei | -0.268 |
gen | 0.000 |
resp | 0.870 |
head | 0.000 |
hr | 0.000 |
cpap | 0.382 |
age | 0.050 |
temp | 0.000 |
size | -0.221 |
Following the lines above, we create a helper function to perform the bootstrap.
glmnet_boot <- function(B, X, y, glmnet_model, weights, var = "resp") {
lambda <- glmnet_model$lambda.min
theta <- as.matrix(coef(glmnet_model, s = lambda))
pi_hat <- predict(glmnet_model, newx = X, s = "lambda.min", type = "response")
n <- length(pi_hat)
y_star <- sapply(seq_len(B), function(i) ifelse(runif(n) <= pi_hat, 1, 0))
beta_star <- apply(y_star, 2,
function(y) {
as.matrix(coef(glmnet::glmnet(x = X, y = y, lambda = lambda, weights = weights, family = "binomial")))
})
rownames(beta_star) <- rownames(theta)
list(theta = theta[var, ],
theta_star = beta_star[var, ],
suff_stat = t(y_star) %*% X)
}
And off we go.
glmnet_boot_out <- glmnet_boot(B = 2000, X, y, glmnet_model, weights)
glmnet_bca <- bcapar(t0 = glmnet_boot_out$theta,
tt = glmnet_boot_out$theta_star,
bb = glmnet_boot_out$suff_stat)
We can compare the output of this against what we got from glm
above.
We can examine the bootstrap limits and statistics.
knitr::kable(glmnet_bca$lims, digits = 3)
bca | jacksd | pct | std | |
---|---|---|---|---|
0.025 | 0.671 | 0.008 | 0.128 | 0.614 |
0.05 | 0.715 | 0.004 | 0.206 | 0.655 |
0.1 | 0.757 | 0.006 | 0.325 | 0.702 |
0.16 | 0.799 | 0.005 | 0.434 | 0.740 |
0.5 | 0.926 | 0.005 | 0.797 | 0.870 |
0.84 | 1.047 | 0.011 | 0.966 | 1.000 |
0.9 | 1.092 | 0.015 | 0.982 | 1.037 |
0.95 | 1.137 | 0.016 | 0.993 | 1.084 |
0.975 | 1.172 | 0.028 | 0.997 | 1.126 |
knitr::kable(glmnet_bca$stats, digits = 3)
theta | sd | a | az | z0 | A | sdd | mean | |
---|---|---|---|---|---|---|---|---|
est | 0.87 | 0.131 | -0.003 | -0.025 | 0.415 | -0.011 | 0.104 | 0.818 |
jsd | 0.00 | 0.002 | 0.010 | 0.012 | 0.023 | 0.034 | 0.004 | 0.003 |
The shrinkage is evident; we now have the bootstrap estimate is now \(0.862\pm 0.127\). In fact, we now have only 0.339 proportion of bootstrap replicates above \(0.862\). Therefore, the bias corrector is large: \(\hat{z}_0 = 0.411.\)
Finally, we can plot both the glm
and glmnet
results side-by-side.
Assume we have two independent estimates of variance from normal theory:
\[ \hat{\sigma}_1^2\sim\frac{\sigma_1^2\chi_{n_1}^2}{n_1}, \]
and
\[ \hat{\sigma}_2^2\sim\frac{\sigma_2^2\chi_{n_2}^2}{n_2}. \]
Suppose now that our parameter of interest is
\[ \theta=\frac{\sigma_1^2}{\sigma_2^2} \]
for which we wish to compute confidence limits. In this setting, theory yields exact limits:
\[ \hat{\theta}(\alpha) = \frac{\hat{\theta}}{F_{n_1,n_2}^{1-\alpha}}. \]
We can apply bcapar
to this problem. As before, here are our helper functions.
ratio_boot <- function(B, v1, v2) {
s1 <- sqrt(v1) * rchisq(n = B, df = n1) / n1
s2 <- sqrt(v2) * rchisq(n = B, df = n2) / n2
theta_star <- s1 / s2
beta_star <- cbind(s1, s2)
list(theta = v1 / v2,
theta_star = theta_star,
suff_stat = beta_star)
}
funcF <- function(beta) {
beta[1] / beta[2]
}
Note that we have an additional function funcF
which corresponds to \(\tau(\hat{\beta}^*)\) in the paper. This is the function expressing the parameter of interest as as a function of the sample.
B <- 16000; n1 <- 10; n2 <- 42
ratio_boot_out <- ratio_boot(B, 1, 1)
ratio_bca <- bcapar(t0 = ratio_boot_out$theta,
tt = ratio_boot_out$theta_star,
bb = ratio_boot_out$suff_stat, func = funcF)
The limits obtained are shown below, along with the exact limits as the last column.
exact <- 1 / qf(df1 = n1, df2 = n2, p = 1 - as.numeric(rownames(ratio_bca$lims)))
knitr::kable(cbind(ratio_bca$lims, exact = exact), digits = 3)
bca | jacksd | pct | std | abc | exact | |
---|---|---|---|---|---|---|
0.025 | 0.412 | 0.008 | 0.068 | -0.053 | 0.405 | 0.422 |
0.05 | 0.475 | 0.007 | 0.103 | 0.117 | 0.472 | 0.484 |
0.1 | 0.559 | 0.007 | 0.164 | 0.312 | 0.562 | 0.570 |
0.16 | 0.639 | 0.006 | 0.228 | 0.466 | 0.646 | 0.650 |
0.5 | 1.046 | 0.006 | 0.570 | 1.000 | 1.057 | 1.053 |
0.84 | 1.772 | 0.025 | 0.903 | 1.534 | 1.813 | 1.800 |
0.9 | 2.095 | 0.032 | 0.953 | 1.688 | 2.154 | 2.128 |
0.95 | 2.573 | 0.043 | 0.985 | 1.883 | 2.726 | 2.655 |
0.975 | 3.141 | 0.096 | 0.996 | 2.053 | 3.416 | 3.247 |
Clearly the bca limits match the exact values very well and suggests a large upward correction to the standard limits. Here the corrections are all positive as seen in the table below; \(\hat{z}_0 = 0.093\) and \(\hat{a} = 0.092\).
knitr::kable(ratio_bca$stats, digits = 3)
theta | sd | a | az | z0 | A | sdd | mean | |
---|---|---|---|---|---|---|---|---|
est | 1 | 0.537 | 0.098 | 0.089 | 0.088 | 0.509 | 0.504 | 1.054 |
jsd | 0 | 0.005 | 0.005 | 0.005 | 0.010 | 0.020 | 0.004 | 0.004 |
knitr::kable(t(ratio_bca$abcstats), digits = 3)
a | z0 |
---|---|
0.1 | 0.1 |
knitr::kable(ratio_bca$ustats, digits = 3)
ustat | sdu | B | |
---|---|---|---|
est | 0.946 | 0.490 | 16000 |
jsd | 0.004 | 0.004 | 0 |
The plot below shows that there is moderate amount of internal error in \(\hat{\theta}_{bca}(0.975)\) as shown by the red bar. The pct
column suggests why: \(\hat{\theta}_{bca}(0.975)\) occurs at the \(0.996\)-quantile of the 16,000 replications, i.e., at the 64th largest \(\hat{\theta}\), where there is a limited amount of data for estimating the distribution.
bcaplot(ratio_bca)
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.