similar to: sem vs. LISREL: sem fails

Hello, I finally run my measurement model in sem - successfully. Now, I am trying to print out the path diagram that is based on the results - but for some reason it's not working. Below is my script - but the problem is probably in my very last line: # ANALYSIS OF ANXIETY, DEPRESSION, AND FEAR - LISREL P.31 library(sem) # Creating the ANXIETY, DEPRESSION, AND FEAR intercorrelation matrix

I am using R and LISREL for simulation studies. R generates the data that is analyzed with LISREL. In LISREL I use "PV" in the LISREL output statement to request estimated variances. LISREL writes these in a file that looks like this: 1 0 0 0.100331D+01 0.144845D+01 0.141009D+01 0.214423D+01 0.214129D+01 0.194464D+01 0.191531D+01 0.198328D+01 0.100683D+00-0.236392D-01

Hi there, as a student sociology, I'm starting to learn about SEM. The course I follow is based on LISREL, but I want to use the SEM-package on R parallel to it. Using LISREL, I found it to be very usable to be able to see the total direct and total indirect effects (standardized and unstandardized) in the output. Can I create these effects using R? I know how to calculate them

Hello ALL! I have a problem to plot factor (lets say gender) as a line, or at least both line and point, from ols model: ols1 <- ols(Y ~ gender, data=dat, x=T, y=T) plot(ols1, gender=NA, xlab="gender", ylab="Y", ylim=c(5,30), conf.int=FALSE) If I convert gender into discrete numeric predictor, and use forceLines=TRUE, plot is not nice and true, since it shows values

I don't know of any R package that can match all the functionality of LEM eg fitting equality constraints to model parameters a la LISREL. WRT dumping tables, I would have thought that as.data.frame.table does pretty much what you want, [not tested] newtab <- as.data.frame(table(a,b,c)) cat("dim\n") for(i in seq(1, ncol(newtab)-1) { cat(nlevels(newtab[,1]," ") }

I am having two problems creating data frames that I have solutions, but they really seem like kludges and I assume I just don't understand the proper R way of doing things. The first situation is I have an set of uneven data vectors. When I try to use them to create a data frame I would like the bottoms of them padded with NAs, without explicitly specifying that. When I do: anxiety.data =

workaround can't be used in wine 1.3.21 winetricks wininet wine iexplore fixme:urlmon:create_object Could not find object for MIME L"application/x-gzip-compressed"

Hi all, I have received the following error from summary.manova: Error in summary.manova(manova.test, test = "Pillai") : residuals have rank 36 < 64 The data is simulated data for 64 variables. The design is a 2*2 factorial with 10 replicates per treatment. Looking at the code for summary.manova, the error involves a problem with qr(). Does anyone have a suggestion as to how to

On 2020-06-19, Justin Hibbits via llvm-dev wrote: >On Fri, 19 Jun 2020 17:38:02 +0100 >Renato Golin <rengolin at gmail.com> wrote: > >> On Fri, 19 Jun 2020 at 16:43, Robinson, Paul via llvm-dev >> <llvm-dev at lists.llvm.org> wrote: >> > If anyone's keeping track of the voting: >> > +1 for "dev" (contrasts with "release")

Hi, I have a set of 30 binary variables measuring side effects after drug treatment. Since each subject can have multiple side effects, I want to display these side effects in a multiple choice table. I'm using the summary and mChoice functions of the Hmisc package, because it produces nicely formatted latex tables. My problem is, that table includes a category for people who have at

On Fri, 19 Jun 2020 14:45:37 +0100 Renato Golin via llvm-dev <llvm-dev at lists.llvm.org> wrote: > On Fri, 19 Jun 2020 at 12:57, Hal Finkel via llvm-dev > <llvm-dev at lists.llvm.org> wrote: > > I like "dev" as an option here. It's short, and in addition, > > conveys the fact that the development happens in that branch. > > "main" in

On Fri, 19 Jun 2020 14:46:19 +0000 "Keane, Erich via llvm-dev" <llvm-dev at lists.llvm.org> wrote: > If the name of our branch causes anxiety/difficulty for a significant > portion of our population, it is literally the least we can do to > choose a word that better respects the last few centuries of world > history. Honestly, if the name of a branch causes

Hi list, I'm performing a series of confirmatory factor analysis on different groupings of items from data collected with questionnaires. There are some missing values. For those sets with no missing values I call factanal(datamatrix,factors=n) where datamatrix is a table of all observations for the items under investigation. This call fails when there are missing values. help(factanal)

Does anyone know if the sem package in R can implement a stacked model comparison, for example as in LISREL or AMOS? Thanks, Anthony -- Anthony Steven Dick, Ph.D. Post-Doctoral Fellow Human Neuroscience Laboratory Department of Neurology The University of Chicago 5841 S. Maryland Ave. MC-2030 Chicago, IL 60637 Phone: (773)-834-7770 Email: adick at uchicago.edu Web:

Hi all, I am trying to get a handle on gls (package nlme). I have a toy problem: 3 fixed factors (A, B, C), two levels each, 5 replicates per treatment. The response variable is continuous, normal. I have a correlation matrix of the form: > mat A B C A 1.00 0.75 0 B 0.75 1.00 0 C 0.00 0.00 1 which is common to all observations. How do I construct the call to gls? I think I need to

A bit late, but you might like to look at http://www.qimr.edu.au/davidD/polyr.R Regarding the original posters queries: You can analyse polychoric correlations as if they were Pearson correlations using standard software (eg sem), and this usually doesn't do too badly, or go to AWLS (Browne) in LISREL etc, or ML analysis of the full multidimensional contingency table using programs such as

Could anyone please explain how to set up contrasts between means in R. I want to know if "before I conduct an experiment and believe the mean for 1 and 2 will be different from means 3 and 4, Is this true?" That is what I have to prove or disprove, I thought that contrasts would be the way to go. Thanks for the help. Igor [[alternative HTML version deleted]]

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Hello, I''ve completed the update of all my servers to the new mongrel. No problems whatsoever to report, well done. But, I have some colleagues who are wondering what the primary improvements are to mongrel with this new release. I read the Change log but it was a bit cryptic for me. Can anyone provide an executive summary of why 1.0.1 is better than 0.3.xx? a few main bullet

Dears, I'm a college student and In doing my statistics homework. I use R with SEM package as my tool for sem analysis, but my teacher told me AMOS is more suitable for such analysis. Could someone help tell me whether it is true that some commercial software is better accepted in academic fields? Sorry if I should not post such topics here. -- Best Regards, Reeyarn T. Lee Accounting