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    <link>http://gmane.org</link>
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  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/313">
    <title>customising the plot() command</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/313</link>
    <description>&lt;pre&gt;Dear Matchit list,

I have a simple question : how can I customize the output of the plot command ?
I am thinking of changing the title,  choosing only  particular
covariates in the QQ plots, etc ...

Many thanks for your help!
Best Regards
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&lt;/pre&gt;</description>
    <dc:creator>Francesco</dc:creator>
    <dc:date>2012-04-27T17:30:40</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/310">
    <title>Converting match matrix results to single column group?</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/310</link>
    <description>&lt;pre&gt;I wish to perform conditional logistic regression on the results of 1:1 matching (eventually 1:N) from MatchIt to both assess the improvement in covariate balance and to analyze outcomes.  Is there any way, using R, to append the match.matrix to the matched dataset as a new column that represents matched pair group numbers (where each grouping represents the two members of the pair?  I plan to use this as a means to perform the conditional logistic regression, conditioned on the matched pair group number.

Thanks for your help,

Bob
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    <dc:creator>McDonald, Robert J., M.D., Ph.D.</dc:creator>
    <dc:date>2012-04-19T16:55:55</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/303">
    <title>Question</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/303</link>
    <description>&lt;pre&gt;Hi Everyone,
   I have a theoretical question. It's been bothering me for a while.
I have a dataset from which I know the treatment is stochastic: 0 &amp;lt;  
Pr(T=1 | X) &amp;lt; 1.
Also I know that Y is independent of T given X. However, T is not  
independent
of Y given X. Does this make sense? Does this violate the theory behind
the potential outcome model? Thanks.

George 
  
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&lt;/pre&gt;</description>
    <dc:creator>georgebaah</dc:creator>
    <dc:date>2012-04-05T15:37:02</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/298">
    <title>matchit() silently adds a propensity score to X whenmethod=='genetic'</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/298</link>
    <description>&lt;pre&gt;
Hello,

     I am writing on behalf of myself and Rocío Titiunik.

     As we see it, matchit() serves as a front end to GenMatch() 
when method=='genetic'.  So it should be possible to get the same 
results from both the MatchIt and Matching packages.  But this 
proves difficult.  Discrepancies seem to occur because matchit() 
silently adds a column of propensity scores to the X matrix that it 
passes to GenMatch().  I'm appending some code that we developed to 
demonstrate this point.

     The benefits (in most cases) of adding a propensity score are 
clear, but it seems problematic that this addition occurs without 
any notification.  For example, a user of MatchIt may claim to have 
matched on a set of predictors, unaware that he has also matched on 
the propensity score.  Or, if a user thinks that he has matched on 
one propensity score (because he included it in X when calling 
matchit()), he will be unaware that he has also matched on a second, 
matchit()-generated propensity score that is based on the first 
propensity score.  In either case, he will be also be unable to 
replicate his MatchIt results with Matching or vice versa, even 
though MatchIt is supposed to be a wrapper for Matching.  And 
third-party readers of code that includes a call to matchit() will 
likely have no idea that a propensity score has been added.

     We can't see any explicit mention of this 
propensity-score-adding feature in the MatchIt manual.  To promote 
future replication efforts, can a line be added to the MatchIt 
manual about the addition of a propensity score to X?  Or can a note 
be added to matchit() output whenever method=='genetic' is used?

Thank you,
John Bullock
###


library(Matching)
library(MatchIt)
data(lalonde)
X &amp;lt;- with(lalonde, cbind(age, educ, black, hispan, married, 
nodegree, re74, re75))

# GET ESTIMATE FROM MATCHIT()
set.seed(5678)
m.out1 &amp;lt;- matchit(treat ~ X, data=lalonde, method='genetic', 
estimand='ATT', ties=TRUE, print.level=1,
                        pop.size=150, wait.generations=1, 
max.generations=10, hard.generation.limit=TRUE,
                        unif.seed=1945, int.seed=1906)

# Create a vector of "parameters at the solution" reported by matchit().
# Behind the scenes, these weights have been produced by GenMatch().
weights &amp;lt;- c(8.121767e+02, 7.735192e+02, 5.938936e+02, 4.079661e+02, 
3.665018e+02, 1.361011e+02,
                  9.644896e+02, 6.083636e+02,  2.346772e+00)

ATT.MatchIt &amp;lt;- with(match.data(m.out1), 
weighted.mean(re78[treat==1], weights[treat==1])) -
                with(match.data(m.out1), 
weighted.mean(re78[treat==0], weights[treat==0]))
print(ATT.MatchIt)  # 939.2


# GET ESTIMATE FROM MATCH()
# The Match() estimate is -952.3 -- very different.
Match(Y=lalonde$re78, Tr=lalonde$treat, X=X, estimand="ATT", 
Weight.matrix=diag(weights), ties=TRUE)$est


# NOTE DISCREPANCY BETWEEN ncol(X) AND length(weights)
# There are only 8 variables in X, so why is matchit() producing 
weights for nine variables?
ncol(X)          # 8
length(weights)  # 9


# ADD PROPENSITY SCORE TO X AND RE-ESTIMATE WITH MATCH()
glm1 &amp;lt;- glm(treat ~ 
age+educ+black+hispan+married+nodegree+re74+re75, family=binomial, 
data=lalonde)
X2 &amp;lt;- with(lalonde, cbind(age, educ, black, hispan, married, 
nodegree, re74, re75))
X2 &amp;lt;- cbind(glm1$fitted, X2)

Match(Y=lalonde$re78, Tr=lalonde$treat, X=X2, estimand="ATT", 
Weight.matrix=diag(weights), ties=TRUE)$est  # 939.2

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    <dc:creator>John G. Bullock</dc:creator>
    <dc:date>2012-03-15T16:48:01</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/296">
    <title>Using matchit for large datasets</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/296</link>
    <description>&lt;pre&gt;Hi, I have the same problem. Which option turns off the calculation of L1?

Regards,
Sotiris



________________________________

if you use CEM and turn off the calculation of L1, its very fast and can

deal with very large data sets.



Gary

--

*Gary King* - Albert J. Weatherhead III University Professor - Director,

IQSS - Harvard University

GKing.Harvard.edu &amp;lt;http://gking.harvard.edu/&amp;gt; - King at Harvard.edu&amp;lt;https://lists.gking.harvard.edu/mailman/listinfo/matchit&amp;gt; -

&amp;lt; at &amp;gt;kinggary&amp;lt;http://twitter.com/kinggary&amp;gt;- 617-500-7570 - Asst 495-9271 -

Fax 812-8581







On Mon, Feb 27, 2012 at 12:14 PM, Donny Baum &amp;lt;donnybaum at gmail.com&amp;lt;https://lists.gking.harvard.edu/mailman/listinfo/matchit&amp;gt;&amp;gt; wrote:









































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    <dc:creator>Adamakis, Sotirios (Customer Analytics &amp; Decision</dc:creator>
    <dc:date>2012-02-28T12:48:21</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/293">
    <title>Using matchit for large datasets</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/293</link>
    <description>&lt;pre&gt;Has anyone come across problems of performance using MatchIt with large
datasets? I am trying to perform nearest neighbor matching with 10
subclassifications on a sample of 400,000 (50,000 treatment cases, 350,00
untreated) with about 25 covariates. I was able to get one round of
successful results after about 8 hours of waiting for R to produce the
output. Is this typical of using MatchIt with large data? Is there any way
to increase the speed or otherwise work around this?

Any help would be great.

Cheers,

Don Baum

&lt;/pre&gt;</description>
    <dc:creator>Donny Baum</dc:creator>
    <dc:date>2012-02-27T17:14:16</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/292">
    <title>(no subject)</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/292</link>
    <description>&lt;pre&gt;Thank You very much Kosuke,

I will check my variables right now.
May I ask you a little methodological question ?

When I use the (logit) propensity matching method , the average propensity score for treated is about 12%...
because only a small part of the treated has scores between 50% and
80%...
Does it means that there is an omitted variable somewhere ? Or there is no absolute reference level and I have to assess this figure relatively to the average score of the control group?
I was expecting to obtain a propensity score much higher for the treated ...  also because when I run the same logistic specification of the probability of bein treated using another stat package (in order to see the significance of the coefficients) I obtain that all my variables are highly significant at the 1% level...

What do you think ?
Many thanks

On 27 February 2012 04:36, Kosuke Imai &amp;lt;kimai&amp;lt; at &amp;gt;princeton.edu&amp;gt; wrote:
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    <dc:creator>Marco Francesco</dc:creator>
    <dc:date>2012-02-27T11:33:04</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/290">
    <title>MAHALANOBIS</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/290</link>
    <description>&lt;pre&gt;Dear Matchit list,

I am using matchit for my work, and I really appreciate the excellent work
you have done so far.
I have a question : I perform a nearest neighbor matching procedure with a
large dataset ( 40 000 individuals, 15 variables) and when I use the
standard propensity score as a distance, everything works fine : the
matching is quite good
However if I specify the "mahalanobis" distance I get an error saying that :

"Lapack dgesv : le système est exactement singulier" (the system is exactly
singular)...

Do you have an idea of what might cause this problem ? I have no missing
data...

Many thanks
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    <dc:creator>Francesco</dc:creator>
    <dc:date>2012-02-24T22:32:01</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/285">
    <title>Trying to implement an example from the MatchIt manual</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/285</link>
    <description>&lt;pre&gt;Hi,
 
I'm trying to implement the example at page 18 from the MatchIt manual. The example is about a way to estimate the ATT.
 
I can't implement the example because I'm using model="ls.mixed" so my dataframe has to be in a long format. In concrete terms, when I extract my dataframe with match.data() to restructure it in long format, I can't use the option data=match.data(mydata, "control") within Zelig.
 
Is there a workaround ? I tried to use matchit() with the long format dataframe, but it gives wrong mathching since each case has multiple observations in that format.
 
Thanks,

François Maurice-
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    <dc:creator>Francois Maurice</dc:creator>
    <dc:date>2012-02-01T19:16:33</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/282">
    <title>ATE or ATT ?</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/282</link>
    <description>&lt;pre&gt;Hi,
 
I'm using MatchIt. I'm trying to understand which method produce ATE estimate and which one produce ATT estimate.
 
In the documentation, section 5: Frequently Asked Questions: How Exactly are the Weights Created?, it is said :
 
"These weights are constructed to estimate the average treatment effect on the treated, [...]".
 
Is there a way with MatchIt to estimate ATE ? To be concrete, I'm using experimental data with a control group almost three times the treated group. I'm using the following four methods with ratio=2 in matchit():
 
Nearest : Drop some controls
Subclassification : Keep all controls
Nearest with exact : Drop some controls
Genetic : Drop some contrls
 
Since subclassification keeps all controls, can that be an ATE estimate or do I need to built my own weights to make sure it is ATE?
 
In general, is MatchIt produced only match set with weights that can only be use to estimate ATT ?
 
And if I use Zelig after MatchIt, is there a way to produce ATE estimate ?
 
Thanks,
 
François Maurice-
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    <dc:creator>Francois Maurice</dc:creator>
    <dc:date>2012-02-01T16:38:42</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/281">
    <title>Another optimal matching question</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/281</link>
    <description>&lt;pre&gt;Hi, again!

I am comparing optimal matching to two nearest neighbor matching methods.
 I ran the PSM in MatchIt! and I am seeing some weird stuff in the
distributions of my covariates for the optimal method.  The standardized
mean differences are very low on average for my simulation runs.  However
the treated and control groups ore very dissimilar in the optimal matching
method.  The covariate distributions in the nearest neighbor methods are
very similar.  How can I explain that?

Thanks!

Shane Phillips
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    <dc:creator>Shane Phillips</dc:creator>
    <dc:date>2012-02-01T15:34:25</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/280">
    <title>Question about optimal matching</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/280</link>
    <description>&lt;pre&gt;Good morning!

I used MatchIt! to run a simulation comparing three different types of
propensity score matching techniques: 1-to-1 Nearest neighbor including
exact matching on two dichotomous variables, 1-to-1 nearest neighbor with a
.1 sd caliper, and 1-to-1 optimal matching.  After conducting 1000 runs of
1600 cases each (134 treated cases and 1466 possible control cases),
optimal showed the lowest average standardized mean difference, but there
was MUCH more variability in the standardized mean difference values than
in the other two methods.  How can I explain this?  All of the methods used
the same data.  There was not much competition for controls.  The nearest
neighbor methods used the default order settings.  Please help!!!!

Thanks,

Shane Phillips
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https://lists.gking.harvard.edu/mailman/listinfo/matchit&lt;/pre&gt;</description>
    <dc:creator>Shane Phillips</dc:creator>
    <dc:date>2012-02-01T12:03:33</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/276">
    <title>Treatments spread over time</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/276</link>
    <description>&lt;pre&gt;Folks,

This is not a matchit question, but I wondered if I could access your wisdom.

Suppose there is a panel dataset, and different units get the
treatment at different dates. That is, there isn't a sharp date on
which the treatment is applied; different units get the treatment on
different dates.

We felt the right estimation strategy would be:

  1 Identify the units that never got treated; they're the control pool
  2 Walk through time. In each time period, identify the firms who are
treated. Find controls using propensity score matching where
information from that time period (only) is used. Once a control has
been used, flag it so it will never be used again.
  3 In this fashion, for each unit that's treated at time t, find a
control at that time t.
  4 Shift everything into event time where the treatment date is defined as 0
  5 Proceed with the analysis as usual.

Would appreciate your insights.

&lt;/pre&gt;</description>
    <dc:creator>Ajay Shah</dc:creator>
    <dc:date>2012-01-01T17:01:50</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/271">
    <title>ATE for Full Matching</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/271</link>
    <description>&lt;pre&gt;Hi!

How would I go about estimating ATE  in R following full matching and
optimal matching in MatchIt?  Would it be any different than the method
shown in the documentation for nearest neighbor matching?

Thanks!

Shane
&lt;/pre&gt;</description>
    <dc:creator>Shane Phillips</dc:creator>
    <dc:date>2011-09-20T00:10:14</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/266">
    <title>ATT question</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/266</link>
    <description>&lt;pre&gt;Hi!

I am trying to calculate ATT for some data, and I am getting an error.
 Below is the relevant code, the error and the traceback...

znn.out&amp;lt;-zelig(growthz~age+cogat+iep*(mapfall+itbs)+lunch*(mapfall+itbs)+treat,
data=match.data(nearest), model="ls")

nnx.out &amp;lt;- setx(znn.out, data = match.data(nearest,"treat"), cond = TRUE)

snn.out &amp;lt;- sim(znn.out, x = nnx.out)


Error in mvrnorm(num, mu = coef(object), Sigma = vcov(object)) :
  incompatible arguments&amp;gt; traceback()6: stop("incompatible arguments")
5: mvrnorm(num, mu = coef(object), Sigma = vcov(object))
4: param.lm(object, num = num, bootstrap = bootstrap)
3: param(object, num = num, bootstrap = bootstrap)
2: sim.cond(znn.out, x = nnx.out)
1: sim(znn.out, x = nnx.out)


Note: Age, cogat, mapfall, and itbs are continuous variables. Iep,
lunch, and treat are binary.


Please help!


S
&lt;/pre&gt;</description>
    <dc:creator>Shane Phillips</dc:creator>
    <dc:date>2011-09-09T14:56:13</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/258">
    <title>incidence density sampling</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/258</link>
    <description>&lt;pre&gt;Hello everyone,

I was wondering if the package has a function to perform incidence density
sampling (case-control sampling).

Tony
&lt;/pre&gt;</description>
    <dc:creator>Galois Theory</dc:creator>
    <dc:date>2011-09-06T17:12:00</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/255">
    <title>exact matching on any algorithm</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/255</link>
    <description>&lt;pre&gt;Dear Matchitlist,

Many thanks for that incredible and useful software that solves
(almost) all my matching problems ...

I would like to know if it is possible to use something similar to the
"exact" option in nearest neighbor matching for all the others
matching algorithms..
That is, for example, apply a genetic algorithm but being able to
obtain matches that have absolutely the same values for, lets say,
their date of birth or any other string or numeric variable...


Many thanks in advance,
Best

&lt;/pre&gt;</description>
    <dc:creator>John Litfiba</dc:creator>
    <dc:date>2011-08-29T13:30:13</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/253">
    <title>Simulation problem</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/253</link>
    <description>&lt;pre&gt;Hi, MatchIt Gurus...

I am running a simulation using MatchIt as part of my dissertation.  I am
trying to compile a dataset of some of the summary data from the MatchIt
procedure (e.g. summary(df, standardized=TRUE)), but I seem to be unable to
do that.  I keep getting the message that that object cannot be coerced into
a dataframe.  Is there anyway that I can export these statistics so that I
can compile the results over many repetitions?


Thanks!

Shane
&lt;/pre&gt;</description>
    <dc:creator>Shane Phillips</dc:creator>
    <dc:date>2011-08-27T00:07:16</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/251">
    <title>Assessing Balance: Variance Ratio</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/251</link>
    <description>&lt;pre&gt;First my complements to all contributors of MatchIt, you really made my life
easier!

Now to my question. I estimated a variety of propensity scores by playing
with several different models: GBM, Logit and then trying out several
matching techniques: Nearest Neighbour (with a variety of calipers), Full
Matching, Subclassification and Genetic Matching.

In the literature I found
&amp;lt;http://www.sciencedirect.com/science/article/pii/S1010794009005727&amp;gt;researchers
to assess the balance by comparing the standardized difference in means and
calculating the variance ratio.

MatchIt summary output shows the standardized difference in means being most
effectively reduced with 1:1 Matching with a Caliper of 0.25 (all covariates
below a 10% level).

Since the t-test was understandably removed in later versions I wonder if
the variance ratio suffered the same fate? Or in other words why is it not
included in the output? And would it be possible to generate it from the
output?

And do you perhaps have any other pointers on how to assess balance or
generally accepted values that indicate a good balance?

Greatly appreciated if someone could point me in the right direction.

Regards,

Paul
&lt;/pre&gt;</description>
    <dc:creator>Paul Diterwich</dc:creator>
    <dc:date>2011-08-23T15:37:39</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/249">
    <title>Distance values from Genetic matching</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/249</link>
    <description>&lt;pre&gt;Hi,
 I'm trying to implement the ideas in Harder, Stuart and Anthony (2010), to seperate the estimation step from the application step and that way to combine various mathcing methods with various distance measures.
 
But I have a problem with genetic mathing. Is there a way to obtain distance values from genetic mathcing (method="genetic") ? The distance values for the genetic method obtain from the matchit() object are the same as those when choosing method="nearest" and distance="logit" (the final results are not the same).
 
Thanks,

François Maurice, B. Sc., A. Stat.
Candidat à la maîtrise
Département de sociologie
Université de Montréal&lt;/pre&gt;</description>
    <dc:creator>Francois Maurice</dc:creator>
    <dc:date>2011-08-14T15:37:44</dc:date>
  </item>
  <item rdf:about="http://comments.gmane.org/gmane.comp.lang.r.matchit/243">
    <title>calculation of std.mean.diff</title>
    <link>http://comments.gmane.org/gmane.comp.lang.r.matchit/243</link>
    <description>&lt;pre&gt;Hi there,

Could you please tell me how is the calculation of the std.mean.diff in the matchit output summary programmed- what is the exact formula used for this standardization (is it standardized according to the SDc and SDt group?)

Many thanks,

Best regards,

Ana&lt;/pre&gt;</description>
    <dc:creator>Ana Kolar</dc:creator>
    <dc:date>2011-08-12T19:37:44</dc:date>
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