I think you are conflating the 1st level and the 2nd level. You could get pcc out of the 2nd level regardless of what you are using for the input from the first level. I've attached a matlab script that will compute the pcc for mri_glmfit output

doug


On 10/04/2013 03:33 PM, Caspar M. Schwiedrzik wrote:
Hi Doug,
I guess it boils down to the question how to get a group PCC map after a RFX GLM? Using -m PCC seems to only give me a map per subject. Are you calculating PCC from the t- values? Thanks,
Caspar


On Thursday, October 3, 2013, Caspar M. Schwiedrzik wrote:

    Hi Doug,

    On Thursday, October 3, 2013, Douglas N Greve wrote:


        It sounds like two issues:
        1. p-values not consistent with your program. What did you use
        to compute? Did you do a two-sided (which is what fsfast uses)?

    I used ttest in Matlab, two sided.

        2. Using pcc maps. Why not use -m pcc?


    Isn't that giving me a map per subject? How do I get the group map
    that is consistent with the results of mri_glmfit run on ces.nii?

    Thanks, Caspar


        doug


        On 10/03/2013 01:10 PM, Caspar M. Schwiedrzik wrote:

            Hi Doug,
            I loaded the pcc.nii file that I got from isxconcat-sess
            into Matlab and then ran a t-test against 0 over the 4th
            dimension. I converted the resulting p-values to -log10
            and then compared them to the output of mri_glmfit, namely
            sig.vol.
            This was the mri_glmfit command:
            mri_glmfit \
            --surf averagesubject hemisphere \
            --y pcc.nii \
            --no-cortex \
            --osgm \
            --glmdir analysisname
            I was expecting the p-values to be the same, which
            apparently is not the case, unless I am
            doing/understanding something wrong.

            By now, I am actually more inclined to use the regression
            coefficients instead. However, I'd still like to get pcc
            maps from them, if there is a way to do so in FSFAST.
            Thanks, Caspar




            2013/10/3 Douglas N Greve <gr...@nmr.mgh.harvard.edu
            <mailto:gr...@nmr.mgh.harvard.edu>>


                On 10/03/2013 10:39 AM, Caspar M. Schwiedrzik wrote:

                    Hi Doug,

                    when I run a two-tailed t-test against 0 in Matlab
            on the Rs
                    in pcc.nii that I get out of isxconcat-sess with
            -m pcc, and
                    DOF from ffxdof.dat, I get different -log10(p)
            values than the
                    ones that come out of mri_glmfit.

                I don't understand what you mean. Can  you elaborate?

                    I am not sure why this is happening.
                    In principle, I just want pcc maps as final output
            to show
                    them on the surface (instead of p-values). So I'd
            be happy to
                    follow your advice regarding the biasing effects
            of noise and
                    autocorrelation and use the regression
            coefficients. However,
                    mri_glmfit (v5.1) does not seem to output pcc maps
            of the
                    contrasts (contrary to selxavg3-sess on the single
            subject
                    level). How would I get those?

                    Thanks, Caspar


                    2013/10/1 Douglas N Greve <gr...@nmr.mgh.harvard.edu
                    <mailto:gr...@nmr.mgh.harvard.edu>
                    <mailto:gr...@nmr.mgh.harvard.edu
                    <mailto:gr...@nmr.mgh.harvard.edu>>>



                        On 10/01/2013 01:13 PM, Caspar M. Schwiedrzik
            wrote:
                        > Hi Doug,
                        > it would be great if you could give me some
            further
                    advise on the
                        > group analysis of functional connectivity maps.
                        > Specifically, I am trying to get PCC maps
            for certain
                    seeds, and am
                        > not planning any comparison between groups.
                        > Following your previous advise, I am running
                    isxconcat-sess with -m
                        > pcc to get the PCC maps.
                        > I would then run
                        >
                        > mri_glmfit \
                        > --surf averagesubject hemisphere \
                        > --y pcc.nii \
                        > --no-cortex \
                        > --osgm \
                        > --glmdir analysisname
                        >
                        > *Could you please provide some more detail
            on what kind of
                        analysis is
                        > performed when I provide pcc.nii as an input for
                    mri_glmfit? Is it a
                        > t-test of the Fisher-transformed r-values
            against 0?
                        I just run a t-test of the r-values. I don't
            have a
                    program to convert
                        them to z-values, however, there are z-values
            that are
                    created in the
                        first level analysis. These are generated from the
                    p-values but I
                        bet it
                        would give you the same thing. Use -m z with
                    isxconcat-sess if you
                        want
                        to use the z.
                        > *Is the average r-value or z-value saved
            somewhere?
                        Which level? For mri_glmfit,  they are not,
            but it is not
                    hard to get
                        them with matlab.
                        > *Do you take the autocorrelation into
            account (as in
                    Vincent JL et
                        > al., 2007. Intrinsic functional architecture
            in the
                    anaesthetized
                        > monkey brain. Nature. 447:83-86)?
                        Not usually, but it could be done by not including
                    -no-whiten when you
                        run mkanalysis-sess. I usually use the regression
                    coefficients instead
                        of correlation coefficients because that they
            are at least
                        unbiased with
                        respect to noise level and autocorrelation.
                        doug


                        > I'd also be happy to look this up but I'd
            need to know
                    where I can


--
Douglas N. Greve, Ph.D.
MGH-NMR Center
gr...@nmr.mgh.harvard.edu
Phone Number: 617-724-2358
Fax: 617-726-7422

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Attachment: mri_glmfit_pcc.m
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