tsci_secondstage {TSCI} | R Documentation |
Two Stage Curvature Identification with User Provided Hat Matrix
Description
tsci_secondstage
implements Two Stage Curvature Identification
(Guo and Buehlmann 2022) for a user-provided hat matrix. Through a data-dependent way it
tests for the smallest sufficiently large violation space among a pre-specified
sequence of nested violation space candidates. Point and uncertainty estimates
of the treatment effect for all violation space candidates including the
selected violation space will be returned amongst other relevant statistics.
Usage
tsci_secondstage(
Y,
D,
Z,
W = NULL,
vio_space,
create_nested_sequence = TRUE,
weight,
A1_ind = NULL,
sel_method = c("comparison", "conservative"),
sd_boot = TRUE,
iv_threshold = 10,
threshold_boot = TRUE,
alpha = 0.05,
intercept = TRUE,
B = 300
)
Arguments
Y |
observations of the outcome variable. Either a numeric vector of length n or a numeric matrix with dimension n by 1. If outcome variable is binary use dummy encoding. |
D |
observations of the treatment variable. Either a numeric vector of length n or a numeric matrix with dimension n by 1. If treatment variable is binary use dummy encoding. |
Z |
observations of the instrumental variable(s). Either a vector of length n or a matrix with dimension n by s. If observations are not numeric dummy encoding will be applied. |
W |
(transformed) observations of baseline covariate(s) used to fit the outcome model. Either a vector of length n
or a matrix with dimension n by p_w or |
vio_space |
list with vectors of length n and/or matrices with n rows as elements to specify the violation space candidates. If observations are not numeric dummy encoding will be applied. See Details for more information. |
create_nested_sequence |
logical. If |
weight |
the hat matrix of the treatment model. |
A1_ind |
indices of the observations that wil be used to fit the outcome model.
Must be of same length as the number of rows and columns of |
sel_method |
The selection method used to estimate the treatment effect. Either "comparison" or "conservative". See Details. |
sd_boot |
logical. if |
iv_threshold |
a numeric value specifying the minimum of the threshold of IV strength test. |
threshold_boot |
logical. if |
alpha |
the significance level. Has to be a numeric value between 0 and 1. |
intercept |
logical. If |
B |
number of bootstrap samples. Has to be a positive integer value.
Bootstrap methods are used to calculate the iv strength threshold if |
Details
The treatment and outcome models are assumed to be of the following forms:
D_i = f(Z_i, X_i) + \delta_i
Y_i = \beta \cdot D_i + h(Z_i, X_i) + \phi(X_i) + \epsilon_i
where f(Z_i, X_i)
is estimated using a random forest,
h(Z_i X_i)
is approximated using the hat matrix weight
provided by the user and
\phi(X_i)
is approximated by a linear combination of the columns in W
.
The errors are allowed to be heteroscedastic. A1
is used to perform violation space selection
and to estimate the treatment effect.
The violation space candidates should be in a nested sequence as the violation space selection is performed
by comparing the treatment estimate obtained by each violation space candidate with the estimates of all
violation space candidates further down the list vio_space
that provide enough IV strength. Only if no
significant difference was found in all of those comparisons, the violation space
candidate will be selected. If sel_method
is 'comparison', the treatment effect estimate of this
violation space candidate will be returned. If sel_method
is 'conservative', the treatment effect estimate
of the successive violation space candidate will be returned provided that the IV strength is large enough.
The specification of suitable violation space candidates is a crucial step because a poor approximation
of g(Z_i, X_i)
might not address the bias caused by the violation of the IV assumption sufficiently well.
The function create_monomials
can be used to create a predefined sequence of
violation space candidates consisting of monomials.
The function create_interactions
can be used to create a predefined sequence of
violation space candidates consisting of two-way interactions between the instrumens themselves and between
the instruments and the instruments and baseline covariates.
The instrumental variable(s) are considered strong enough for violation space candidate V_q
if the estimated IV strength using this
violation space candidate is larger than the obtained value of the threshold of the IV strength.
The formula of the threshold of the IV strength has the form
\min \{\max \{ 2 \cdot \mathrm{Trace} [ \mathrm{M} (V_q) ], \mathrm{iv{\_}threshold} \} + S (V_q), 40 \}
if threshold_boot
is TRUE
, and
\min \{\max \{ 2 \cdot \mathrm{Trace} [ \mathrm{M} (V_q) ], \mathrm{iv{\_}threshold} \}, 40 \}
if threshold_boot
is FALSE
. The matrix
\mathrm{M} (V_q)
depends on the hat matrix obtained from estimating f(Z_i, X_i)
, the violation space candidate V_q
and
the variables to include in the outcome model W
. S (V_q)
is obtained using a bootstrap and aims to adjust for the estimation error
of the IV strength.
Usually, the value of the threshold of the IV strength obtained using the bootstrap approach is larger.
Thus, using threshold_boot
equals TRUE
leads to a more conservative IV strength test.
For more information see subsection 3.3 in Guo and Buehlmann (2022).
See also Carl et al. (2023) for more details.
Value
A list containing the following elements:
Coef_all
a series of point estimates of the treatment effect obtained by the different violation space candidates.
sd_all
standard errors of the estimates of the treatmnet effect obtained by the different violation space candidates.
pval_all
p-values of the treatment effect estimates obtained by the different violation space candidates.
CI_all
confidence intervals for the treatment effect obtained by the different violation space candidates.
Coef_sel
the point estimator of the treatment effect obtained by the selected violation space candidate(s).
sd_sel
the standard error of Coef_sel.
pval_sel
p-value of the treatment effect estimate obtained by the selected violation space candidate(s).
CI_sel
confidence interval for the treatment effect obtained by the selected violation space candidate(s).
iv_str
IV strength using the different violation space candidates.
iv_thol
the threshold for the IV strength using the different violation space candidates.
Qmax
the violation space candidate that was the largest violation space candidate for which the IV strength was considered large enough determined by the IV strength test. If 0, the IV Strength test failed for the first violation space candidate. Otherwise, violation space selection was performed.
q_comp
the violation space candidate that was selected by the comparison method over the multiple data splits.
q_cons
the violation space candidate that was selected by the conservative method over the multiple data splits.
invalidity
shows whether the instrumental variable(s) were considered valid, invalid or too weak to test for violations. The instrumental variables are considered too weak to test for violations if the IV strength is already too weak using the first violation space candidate (besides the empty violation space). Testing for violations is always performed by using the comparison method.
References
Zijian Guo, and Peter Buehlmann. Two Stage Curvature Identification with Machine Learning: Causal Inference with Possibly Invalid Instrumental Variables. arXiv:2203.12808, 2022
Nicolai Meinshausen, Lukas Meier, and Peter Buehlmann. P-values for high-dimensional regression. Journal of the American Statistical Association, 104(488):1671-1681, 2009. 16, 18
Victor Chernozhukov, Denis Chetverikov, Mert Demirer, Esther Duflo, Christian Hansen, Whitney Newey, and James Robins. Double/debiased machine learning for treatment and structural parameters: Double/debiased machine learning. The Econometrics Journal, 21(1), 2018. 4, 16, 18
David Carl, Corinne Emmenegger, Peter Buehlmann, and Zijian Guo. TSCI: two stage curvature identification for causal inference with invalid instruments. arXiv:2304.00513, 2023
See Also
tsci_boosting
for TSCI with boosting.
tsci_forest
for TSCI with random forest.
tsci_poly
for TSCI with polynomial basis expansion.
Examples
### a small example without baseline covariates
if (require("MASS")) {
# sample size
n <- 100
# the IV strength
a <- 1
# the violation strength
tau <- 1
# true effect
beta <- 1
# treatment model
f <- function(x) {1 + a * (x + x^2)}
# outcome model
g <- function(x) {1 + tau * x}
# generate data
mu_error <- rep(0, 2)
Cov_error <- matrix(c(1, 0.5, 0.5, 1), 2, 2)
Error <- MASS::mvrnorm(n, mu_error, Cov_error)
# instrumental variable
Z <- rnorm(n)
# treatment variable
D <- f(Z) + Error[, 1]
# outcome variable
Y <- beta * D + g(Z) + Error[, 2]
# Two Stage User Defined
# get hat matrix of treatment model
A <- cbind(1, Z, Z^2, Z^3)
weight <- A %*% chol2inv(chol(t(A) %*% A)) %*% t(A)
# create violation space candidates
vio_space <- create_monomials(Z, 2, "monomials_main")
# perform two stage curvature identification
output_UD <- tsci_secondstage(Y, D, Z, vio_space = vio_space, weight = weight,
B = 100)
summary(output_UD)
}