metaSEM

accumulative sample size
Dear Mike,
Is there an approach to compute the accumulative sample size (N)?
It is quite convenient to know the number of primary studies (n) by "pattern.na ( )", but I can't find a syntax for the accumulative sample size (N).
Thanks in advance!
Ryan
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An error in stage-1 for fixed model
Dear Mike,
I encounter a problem when trying the fixed model for stage 1. The error info is
"Error in if (!all(isPD)) stop(paste("Group ", (1:no.groups)[!isPD], " is not positive definite.", :
missing value where TRUE/FALSE needed".
The dataset is exactly the same one I used in random model. I tried "fixed1<-tssem1(my.df, n, method="FEM", no.string="NA")", and NA is the expression in my dataset for missing values, but metaSEM seems not to accept this argument.
Would you please provide any hints?
Thanks!
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Increasing the number of replication from default(50) to 5000
Dear Mike,
When I call summary (random2a, R=5000), z-values and standard errors of some estimates are significantly changed. The estimates and goodness-of-fit indices remain the same.
I didn't try (R=10000), as "R=5000" already took 7 hours to finish;)
However, if the number of replications dramatically influences the z-values and std.errors, are there any criteria for choosing one result for reporting?
Thanks!
Ryan

TSSEM_stage2_output:(1)inconsistent results,(2)unsatisfactory CFI & TLI
Dear Mike,
After struggling with my data in the stage 1 of TSSEM, I finally moved into the stage 2. However, the output seems not to be very good.
(1) The results of two approaches of specifying models are different.
Specifically, when using "diag.constraints=TRUE, intervals.type="z"", the result suggests "Amatrix[1,22]" and "Amatrix[1,23]" are significant. But removing the "constraints" and "intervals.type", the result suggests "Amatrix[1,21]" is significant.
In addition, both results have same goodness-of-fit values. Which result I should believe?

Model specification (fix factor loading or latent variable variance).
Hello All,
As the title suggests, I have a question regarding whether to fix the factor loading or the latent variable variance. Both can be fixed in order to derive a 'scale' for your latent variables. The fit statistics should be the same in both cases.

"x is not positive definite"
Hi all,
I encounter a problem of "x is not positive definite" when using Cheung's Two-stage MASEM. Could anyone provide some clues?
I attach part of my dataset as samples. My R-syntax is "random1<-tssem1(entrymode,samplesize,method="REM",RE.type="Diag")" . This command ends with an error information:
Error in (function(x, n, cor.analysis = TRUE, dropNA = FALSE, as.matrix = TRUE), : x is not positive definite!
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Formative Model with TSSEM
Hi there,
I am using A/Prof Mike Cheung's TSSEM (See: https://dl.dropboxusercontent.com/u/25182759/Fixed%20and%20Random%20Effects%20Meta%20Analytic%20Structural%20Equation%20Modeling.pdf). The 2nd stage of this method is constructing a path model (a SEM model) based on the A, S, and F matrices of OpenMx.
Mike's examples (as well as the examples of OpenMx) show only 'reflective models' (i.e., the arrows of paths are from a latent variable to its elements.
My question is: can we build formative models (i.e., the arrows of paths are from elements to a latent variable)?
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Paths appear to be fixed to 1.000 when fitting the structural model in Stage 2.
Dr. Mike,
I am running multiple structural models and appear to have the same issue with all the models. In each of the outputs the certain paths appear to be fixed to 1.0 and another value.
For instance in the structural model, EU -> BI -> U (files EUBIU.dat & EUBIU.R), the paths from EU -> BI = 1 and the path from BI -> U = 1.
Another model (files PUEUBI.data & PUEUBI.R), the paths EU -> PU = 1.0, while the paths from EU -> BI and PU -> BI are both equal to 1.0.
I think I may be constraining these paths to be either equal to 1.0 or equal to each other.

metaSEM and control variables
Dear all,
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what if three level turned out to be unnecessary?
After model comparison with 'anova()' command, variation in level 3 turned out to be not significant which means that 3 level approach can be inappropriate for the data.
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