similar to: New Package for Multivariate and Propensity Score Matching

We would like to announce the availability on CRAN of a new package multinomRob. It does robust estimation of overdispersed multinomial regression models. The package is also able to estimate overdispersed grouped multinomial logistic and multivariate-t logistic models. The code is relatively general; for example, it allows for equality constraints across parameters and it can handle datasets in

We would like to announce the availability on CRAN of a new package multinomRob. It does robust estimation of overdispersed multinomial regression models. The package is also able to estimate overdispersed grouped multinomial logistic and multivariate-t logistic models. The code is relatively general; for example, it allows for equality constraints across parameters and it can handle datasets in

Hi all, i am looking to built a simple example of a very basic propensity score adjustment, just using the estimated propensity scores as inverse probability weights (respectively 1-estimated weights for the non-treated). As far as i understood, MLE predictions of a logit model can directly be used as to estimates of the propensity score. I already considered the twang package and the

I'm using the "Match" package to do propensity score matching. Here's some example code that shows the problem that I'm having (much of this code is taken from the Match package documentation): *data(lalonde) glm1 <- glm(treat~age + I(age^2) + educ + I(educ^2) + black + hisp + married + nodegr + re74 + I(re74^2) + re75 + I(re75^2) + u74 + u75,

There may be benefits to having a machine learning method that explicitly targets covariate balance. We have experimented with optimizing the weights directly to obtain the best covariate balance, but got some strange solutions for simple cases that made us wary of such methods. Machine learning methods that yield calibrated probability estimates should do well (e.g. those that optimize the

Dear R-list, i have 6 different sets of samples. Each sample has about 5000 observations, with each observation comprised of 150 baseline covariates (X), 125 of which are dichotomous. Roughly 20% of the observations in each sample are "treatment" and the rest are "control" units. i am doing propensity score matching, i have already estimated propensity scores(predicted

Dear All, My question is more a statistical question than a R question. The reason I am posting here is that there are lots of excellent statistician on this list, who can always give me good advices. Per my understanding, the purpose of propensity score is to reduce the bias while estimating the treatment effect and its implementation is a 2-stage model. 1) First of all, if we assume that T =

Dear everyone, I am trying to run rgenoud on several chips simultaneusly. I used the instructions provided on Jasjeet Sekhon's Homepage (http://sekhon.berkeley.edu/rgenoud/multiple_cpus.html). However, I have the newer version of R (R 2.12) installed - for a 64-bit machine. So, when I tried to install the special version of "snow" from a zip file provided by Jasjeet on his page, R

Dear All, I would like to find something ( references, code,..) to implement a comparison of three treatments in an observational study using the 'Propensity Score'. Any help is much appreciated. Thanks! Giovanni -- dr. Giovanni Parrinello Department of Biotecnologies Medical Statistics Unit University of Brescia Viale Europa, 11 25123 Brescia email: parrinel at med.unibs.it Phone:

Dear List, I am having difficulty running the ps() function when variables are stored as factors and was hoping someone could provide some advice on how to proceed. I am running propensity score matching as outlined in: Greg Ridgeway, Dan McCarey, Andrew Morral, Lane Burgette and Beth Ann Grin (May 3, 2013) Toolkit for Weighting and Analysis of Nonequivalent Groups: A tutorial for the twang

Hi all, i am wondering if there?s any other method to adjust for selection related bias of estimates except propensity scoring and heckit / mills ratio approach? i also read documentation of Match and twang package so far, so i don?t speak of any ATE / ATT related methods, respectively any methods that match or stratify... Is there something else ? thx in advance

I would like to limit the significant figures of the calibrated parameters determined by genoud() in the Rgenoud package. Below is some example output, where column 1 is model run number, columns 2-7 are the parameter values, and columns 8-12 are model fit statistics. I would like genoud to internally limit parameters to 4 decimal places as shown in this output. It is clear that the function is

Hi. I am using the Matching package for propensity score matching. For each treated unit, I want to find all control units whose propensity scores lie within a certain distance from the treated unit. The sample code is as follows: > library(Matching) > x <- rnorm(100000) > y <- rnorm(100000) > z <- rbinom(100000,1,0.002) > logit.reg <-

Hola chic en s, alguien con experiencia en propensión score matching? Planteo duda: Clasicamente el PSM se ha utilizado en un intento de homogeneizar cohortes de enfermos quienes han estado ?expuestos? a un tratamiento x Vs aquellos que no han estado expuestos (no expuestos). Esto aplica para medicamentos o procedimientos quirúrgicos o no. Bien, En algún articulo he leído que el PSM se puede

Hello all. I am doing one part of an evaluation of a mandatory welfare-to-work programme in the UK. As with all evaluations, the problem is to determine what would have happened if the initiative had not taken place. In our case, we have a number of pilot areas and no possibility of random assignment. Therefore we have been given control areas. My problem is to select for survey individuals in

Hola chic en s, alguien con experiencia en propensión score matching? Planteo duda: Clasicamente el PSM se ha utilizado en un intento de homogeneizar cohortes de enfermos quienes han estado ?expuestos? a un tratamiento x Vs aquellos que no han estado expuestos (no expuestos). Esto aplica para medicamentos o procedimientos quirúrgicos o no. Bien, En algún articulo he leído que el PSM se puede

Dear R-help: Has anyone tried using R on the the AMD Opteron in either 64- or 32-bit mode? If so, any good/bad experiences, comments, etc? We are considering getting this hardware, and would like to know if R can run smoothly on such a beast. Any comment much appreciated. Best, Andy Andy Liaw, PhD Biometrics Research PO Box 2000, RY33-300 Merck Research Labs Rahway, NJ

Hello, I am trying to do model autocalibration using the snow and rgenoud packages. The function I want to run in task-parallel fashion across multiple machines is one that pre- and post-processes data and runs an external model code. My problem is that external file I/O is happening only in the master node and not in the slaves. I have followed Jasjeet Sekhon's suggestion to test the

Dear All I am using rgenoud to solve the following maximization problem: myfunc <- function(x) { x1 <- x[1] x2 <- x[2] if (x1^2+x2^2 > 1) return(-9999999) else x1+x2 } genoud(myfunc, nvars=2, Domains=rbind(c(0,1),c(0,1)),max=TRUE,boundary.enforcement=2,solution.tolerance=0.000001) How can one increase the precision of the solution $par [1] 0.7072442 0.7069694 ? I

Hello! If I understand this listserve correctly, I can email this address to get help when I am struggling with code. If this is inaccurate, please let me know, and I will unsubscribe. I have been struggling with the same error message for a while, and I can't seem to get past it. Here is the issue: I am using a data set that uses -1:-9 to indicate various kinds of missing data. I changed