Yes, pretty much:  I usually have a study directory into which I copy the 
Conte69 files.  Then I rename the Conte69 spec to something more 
study-specific.  I usually use the Conte69 inflated and very inflated for t-map 
visualization, along with mean group mid thickness (both medial/lateral surface 
views, but also overlaid as contours on volume slices).

I don't usually use the TFCE column for visualization, and if I recall 
correctly, there might be p-value and q-value (1-p, which works better with the 
Caret thresholding) columns.  This can tell you how close to significance you 
got.

And yes:  You use the D/C Overlay/Underlay surface menu to control what is 
displayed, which column, etc.


On Feb 3, 2014, at 6:10 PM, Eshita Shah <[email protected]> wrote:

> Yes, that's what I was afraid of. I was expecting significant differences 
> between the two groups. But thanks for clarifying. 
> 
> I am still a bit confused on how exactly to load the metric files on the 
> Conte69 atlas. Do I open up the Conte69 spec and "add data files" in the menu 
> to open up TFCE files? And then do I overlay it using D/C --> 
> Overlay/Underlay Surfaces --> Primary Overlay, etc.? 
> 
> Again, thank you for all your help. 
> 
> Eshita 
> 
> 
> On Mon, Feb 3, 2014 at 3:49 PM, Donna Dierker <[email protected]> 
> wrote:
> No, I think the problem is that nothing survived TFCE thresholding.  If it 
> had, you would see an entry (or more) under the column heads (Column, Thresh, 
> Num-Nodes, etc.).  There is no entry, which means nothing survived.
> 
> Column    Thresh  Num-Nodes          Area  Area-Corrected     COG-X     COG-Y
>   COG-Z   P-Value
> 
> TFCE           P
> 
> You can try loading your f-map 
> (ANOVA_29-01-14.OCD_CTRL.Depth.LH.fmap.significant.tfce.1.0E.2.0H.73730.metric)
>  and switch to the TFCE column, and apply thresholds corresponding to the 
> list of values right under the column heads, so you can see how close/far you 
> were.
> 
> I am under the weather right now, so I will have another look at this 
> tomorrow, but I honestly think you are interpreting it correctly.  If you are 
> like me, you probably are disappointed with these results.  (There are 
> exceptions, of course.)
> 
> 
> On Feb 3, 2014, at 4:37 PM, Eshita Shah <[email protected]> wrote:
> 
> > Donna,
> >
> > Thank you so much for your thorough response. What I'm worried about as of 
> > now is the significance.report.txt file. I have uploaded it using the link 
> > you provided, please let me know if there is anything unusual. When I ran 
> > ANOVA without TFCE, I had rows of information right below the header, as 
> > you mentioned. But for the TFCE report, I don't see anything similar. Maybe 
> > I am interpreting it incorrectly?
> >
> > Thank you,
> > Eshita
> >
> >
> > On Fri, Jan 31, 2014 at 1:15 PM, Donna Dierker 
> > <[email protected]> wrote:
> > On Jan 31, 2014, at 2:17 PM, Eshita Shah wrote:
> >
> >> Hi Donna,
> >>
> >> Yes! I was able to successfully get past the issue of JRE halting-- I just 
> >> installed the latest JRE as Tim suggested, and added some options for 
> >> garbage collection so that it would optimize memory use. Thank you for all 
> >> your help!
> >>
> >> I have computed one mean midthickness for all my subjects, but 
> >> specifically how do I overlay that onto an anatomical template? Would 
> >> there be any advantage of using the NIFTI volume vs. using an average 
> >> volume created from my subject pool?
> >
> > One advantage of using the template used for stereotaxic/volumetric 
> > registration, if any was done, is that it is standard.  Reviewers and 
> > readers are more familiar with it, and don't have to understand how it was 
> > generated.  This is just for display/orientation -- not for analysis.
> >
> > Another is that you don't have the extra step of computing a mean volume.
> >
> >> f so, how would I be able to generate that average volume?
> >
> > I usually use AFNI's 3dMean when I need to do this, but FSL, SPM, and other 
> > packages have similar features.  Maybe wb_command supports it now.  You can 
> > probably do it in multiple steps with caret_command, but it's a pain.
> >
> >> I am also a bit unclear on how to interpret and draw conclusions from the 
> >> outputs of TFCE. I understand that TFCE creates many .metric files 
> >> including one that indicates all the significant differences between the 
> >> two groups. How can I overlay that (along with the .label file) onto a 
> >> surface in Caret?
> >
> > I usually generate a border about the cluster in the label.gii file and 
> > overlay it on the unthresholded t-map, so that users can see subthreshold 
> > diffs.  I display the t-map on the inflated atlas surface (Conte69, if I 
> > recall correctly here).  If there are diffs in the insula/operculum, i use 
> > the very inflated surface, which shows them more clearly.
> >
> >> (Where does the mean midthickness come into play?)
> >
> > Sometimes it is evident just by comparing the mean midthickness surfaces 
> > that there is a difference.  Other times, you need to look at a slice view 
> > of the template with group contours overlaid at a slice that best shows the 
> > diffs.  Could be coronal, axial, or sagittal.
> >
> >> Also, how do I interpret the results written in the significance.report 
> >> text file?
> >
> > If you upload your report, I can tell you the lines to focus on:
> >
> > http://brainvis.wustl.edu/cgi-bin/upload.cgi
> >
> > They should be near the top, just below a header that lists the column, 
> > number of nodes, corrected and uncorrected areas, x, y, z, etc.  I'm 
> > psyched you got this far!  I was feeling frustrated after you ran into the 
> > JRE problem.  I'm glad you got past it.
> >
> >> Thank you so much.
> >>
> >> Sincerely,
> >> Eshita
> >>
> >>
> >> On Thu, Jan 30, 2014 at 5:17 PM, Donna Dierker 
> >> <[email protected]> wrote:
> >> Wow, does this mean you got past the grind-to-a-halt JRE problem?  
> >> Excellent!
> >>
> >> Here is a script I used to compute mean midthickness surfaces for two 
> >> groups:
> >>
> >> http://brainmap.wustl.edu/pub/donna/US/UCLA/ESHITA/gen_mean_fiducials.pared.sh
> >> login pub
> >> password download
> >>
> >> But the main command is this one:
> >>
> >> caret_command -surface-average $OUTCOORD $COORD1 $COORD2 … $COORDn $SHAPE
> >>
> >> The $SHAPE is a vertex:scalar mapping identical in format to a metric, but 
> >> it stores the 3D variability for each vertex.
> >>
> >> You can visualize multiple mean coord files (e.g., one for each DX group) 
> >> overlaid on the same anatomical volume (e.g., avg152T1) and click on hot 
> >> spots on your metric, to see if the contours diverge there.  You can also 
> >> compute the distance between the two surfaces directly on the Surface: 
> >> Measures menu (if I recall correctly).
> >>
> >> Sounds like you're making great progress!
> >>
> >>
> >> On Jan 30, 2014, at 5:27 PM, Eshita Shah <[email protected]> wrote:
> >>
> >> > Hello,
> >> >
> >> > I have created metric files from my TFCE statistical analysis that I 
> >> > wish to view on my own study-specific generated average coordinate file. 
> >> > How would I go about doing so? I do have the Conte69 Visualization 
> >> > Atlas, but I am not sure how to overlay the metric files generated by 
> >> > TFCE to visualize significant clusters. I would eventually like to do 
> >> > this overlay on my own average file, not the 164k averages.
> >> >
> >> > Thank you,
> >> > Eshita
> >> >
> >> > --
> >> > Eshita Shah
> >> > University of California, Los Angeles | 2014
> >> > B.S. Neuroscience
> >> > [email protected]
> >> >
> >> >
> >> > _______________________________________________
> >> > caret-users mailing list
> >> > [email protected]
> >> > http://brainvis.wustl.edu/mailman/listinfo/caret-users
> >>
> >>
> >> _______________________________________________
> >> caret-users mailing list
> >> [email protected]
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> >>
> >>
> >>
> >> --
> >> Eshita Shah
> >> University of California, Los Angeles | 2014
> >> B.S. Neuroscience
> >> [email protected]
> >>
> >>
> >> _______________________________________________
> >> caret-users mailing list
> >> [email protected]
> >> http://brainvis.wustl.edu/mailman/listinfo/caret-users
> >
> >
> > _______________________________________________
> > caret-users mailing list
> > [email protected]
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> >
> >
> >
> >
> > --
> > Eshita Shah
> > University of California, Los Angeles | 2014
> > B.S. Neuroscience
> > [email protected]
> >
> >
> > _______________________________________________
> > caret-users mailing list
> > [email protected]
> > http://brainvis.wustl.edu/mailman/listinfo/caret-users
> 
> 
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> 
> 
> 
> -- 
> Eshita Shah
> University of California, Los Angeles | 2014
> B.S. Neuroscience 
> [email protected] 
> 
> 
> _______________________________________________
> caret-users mailing list
> [email protected]
> http://brainvis.wustl.edu/mailman/listinfo/caret-users


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