method_genetic | R Documentation |
In matchit()
, setting method = "genetic"
performs genetic matching.
Genetic matching is a form of nearest neighbor matching where distances are
computed as the generalized Mahalanobis distance, which is a generalization
of the Mahalanobis distance with a scaling factor for each covariate that
represents the importance of that covariate to the distance. A genetic
algorithm is used to select the scaling factors. The scaling factors are
chosen as those which maximize a criterion related to covariate balance,
which can be chosen, but which by default is the smallest p-value in
covariate balance tests among the covariates. This method relies on and is a
wrapper for \pkgfunMatchingGenMatch and \pkgfunMatchingMatch, which use
\pkgfunrgenoudgenoud to perform the optimization using the genetic
algorithm.
This page details the allowable arguments with method = "genetic"
.
See matchit()
for an explanation of what each argument means in a general
context and how it can be specified.
Below is how matchit()
is used for genetic matching:
matchit(formula, data = NULL, method = "genetic", distance = "glm", link = "logit", distance.options = list(), estimand = "ATT", exact = NULL, mahvars = NULL, antiexact = NULL, discard = "none", reestimate = FALSE, s.weights = NULL, replace = FALSE, m.order = NULL, caliper = NULL, ratio = 1, verbose = FALSE, ...)
formula |
a two-sided formula object containing the treatment and covariates to be used in creating the distance measure used in the matching. This formula will be supplied to the functions that estimate the distance measure and is used to determine the covariates whose balance is to be optimized. |
data |
a data frame containing the variables named in |
method |
set here to |
distance |
the distance measure to be used. See |
link |
when |
distance.options |
a named list containing additional arguments
supplied to the function that estimates the distance measure as determined
by the argument to |
estimand |
a string containing the desired estimand. Allowable options
include |
exact |
for which variables exact matching should take place. |
mahvars |
when a distance corresponds to a propensity score (e.g., for
caliper matching or to discard units for common support), which covariates
should be supplied to the generalized Mahalanobis distance matrix for
matching. If unspecified, all variables in |
antiexact |
for which variables ant-exact matching should take place.
Anti-exact matching is processed using the |
discard |
a string containing a method for discarding units outside a
region of common support. Only allowed when |
reestimate |
if |
s.weights |
the variable containing sampling weights to be incorporated
into propensity score models and balance statistics. These are also supplied
to |
replace |
whether matching should be done with replacement. |
m.order |
the order that the matching takes place. Allowable options
include |
caliper |
the width(s) of the caliper(s) used for caliper matching. See Details and Examples. |
std.caliper |
|
ratio |
how many control units should be matched to each treated unit for k:1 matching. Should be a single integer value. |
verbose |
|
... |
additional arguments passed to \pkgfunMatchingGenMatch.
Potentially useful options include |
In genetic matching, covariates play three roles: 1) as the variables on
which balance is optimized, 2) as the variables in the generalized
Mahalanobis distance between units, and 3) in estimating the propensity
score. Variables supplied to formula
are always used for role (1), as
the variables on which balance is optimized. When distance
corresponds to a propensity score, the covariates are also used to estimate
the propensity score (unless it is supplied). When mahvars
is
specified, the named variables will form the covariates that go into the
distance matrix. Otherwise, the variables in formula
along with the
propensity score will go into the distance matrix. This leads to three ways
to use distance
and mahvars
to perform the matching:
When distance
corresponds to a propensity score and mahvars
is not specified, the covariates in formula
along with the
propensity score are used to form the generalized Mahalanobis distance
matrix. This is the default and most typical use of method = "genetic"
in matchit()
.
When distance
corresponds to a propensity score and mahvars
is specified, the covariates in mahvars
are used to form the
generalized Mahalanobis distance matrix. The covariates in formula
are used to estimate the propensity score and have their balance optimized
by the genetic algorithm. The propensity score is not included in the
generalized Mahalanobis distance matrix.
When distance
is a method of computing a distance matrix
(e.g.,"mahalanobis"
), no propensity score is estimated, and the
covariates in formula
are used to form the generalized Mahalanobis
distance matrix. Which specific method is supplied has no bearing on how the
distance matrix is computed; it simply serves as a signal to omit estimation
of a propensity score.
When a caliper is specified, any variables mentioned in caliper
,
possibly including the propensity score, will be added to the matching
variables used to form the generalized Mahalanobis distance matrix. This is
because Matching doesn't allow for the separation of caliper
variables and matching variables in genetic matching.
The estimand
argument controls whether control
units are selected to be matched with treated units (estimand = "ATT"
) or treated units are selected to be matched with control units
(estimand = "ATC"
). The "focal" group (e.g., the treated units for
the ATT) is typically made to be the smaller treatment group, and a warning
will be thrown if it is not set that way unless replace = TRUE
.
Setting estimand = "ATC"
is equivalent to swapping all treated and
control labels for the treatment variable. When estimand = "ATC"
, the
default m.order
is "smallest"
, and the match.matrix
component of the output will have the names of the control units as the
rownames and be filled with the names of the matched treated units (opposite
to when estimand = "ATT"
). Note that the argument supplied to
estimand
doesn't necessarily correspond to the estimand actually
targeted; it is merely a switch to trigger which treatment group is
considered "focal". Note that while GenMatch()
and Match()
support the ATE as an estimand, matchit()
only supports the ATT and
ATC for genetic matching.
All outputs described in matchit()
are returned with
method = "genetic"
. When replace = TRUE
, the subclass
component is omitted. When include.obj = TRUE
in the call to
matchit()
, the output of the call to \pkgfunMatchingGenMatch will be
included in the output.
In a manuscript, be sure to cite the following papers if using
matchit()
with method = "genetic"
:
Diamond, A., & Sekhon, J. S. (2013). Genetic matching for estimating causal effects: A general multivariate matching method for achieving balance in observational studies. Review of Economics and Statistics, 95(3), 932–945. \Sexpr[results=rd]{tools:::Rd_expr_doi("10.1162/REST_a_00318")}
Sekhon, J. S. (2011). Multivariate and Propensity Score Matching Software with Automated Balance Optimization: The Matching package for R. Journal of Statistical Software, 42(1), 1–52. \Sexpr[results=rd]{tools:::Rd_expr_doi("10.18637/jss.v042.i07")}
For example, a sentence might read:
Genetic matching was performed using the MatchIt package (Ho, Imai, King, & Stuart, 2011) in R, which calls functions from the Matching package (Diamond & Sekhon, 2013; Sekhon, 2011).
matchit()
for a detailed explanation of the inputs and outputs of
a call to matchit()
.
MatchingGenMatch and \pkgfunMatchingMatch, which do the work.
data("lalonde")
# 1:1 genetic matching with PS as a covariate
m.out1 <- matchit(treat ~ age + educ + race + nodegree +
married + re74 + re75, data = lalonde,
method = "genetic",
pop.size = 10) #use much larger pop.size
m.out1
summary(m.out1)
# 2:1 genetic matching with replacement without PS
m.out2 <- matchit(treat ~ age + educ + race + nodegree +
married + re74 + re75, data = lalonde,
method = "genetic", replace = TRUE,
ratio = 2, distance = "mahalanobis",
pop.size = 10) #use much larger pop.size
m.out2
summary(m.out2, un = FALSE)
# 1:1 genetic matching on just age, educ, re74, and re75
# within calipers on PS and educ; other variables are
# used to estimate PS
m.out3 <- matchit(treat ~ age + educ + race + nodegree +
married + re74 + re75, data = lalonde,
method = "genetic",
mahvars = ~ age + educ + re74 + re75,
caliper = c(.05, educ = 2),
std.caliper = c(TRUE, FALSE),
pop.size = 10) #use much larger pop.size
m.out3
summary(m.out3, un = FALSE)
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