I'm not sure that I understand what I'm looking at. If it is an ROI 
analysis, then there is no surface, it should be about 40 numbers, one 
for each ROI.

On 02/03/2015 06:26 PM, Bronwyn Overs wrote:
> Hi Doug,
>
> Thanks for your correction.
>
> I have now completed the FDR for my case-control comparisons, and it 
> appears that none of the regions survived. This is again quite 
> confusing given the large number of parcellated regions that survived 
> FDR in the SPSS ANCOVA. Can you confirm that this screenshot of the 
> sig.mgh file from ROI analysis looks as you would expect (it looks 
> very strange to me):
>
>
>
> Kind regards,
>
> Bronwyn Overs
> Research Assistant
>
> Neuroscience Research Australia
>
> Neuroscience Research Australia
> Margarete Ainsworth Building
> Barker Street Randwick Sydney NSW 2031 Australia
> *M* 0411 308 769 *T* +61 2 9399 1883 *F* +61 2 9399 1265
>
> neura.edu.au <http://neura.edu.au>
>
> Follow @neuraustralia on twitter 
> <https://twitter.com/neuraustralia>Follow NeuRA on facebook 
> <https://www.facebook.com/NeuroscienceResearchAustralia>Subscribe to 
> the NeuRA Magazine <http://www.neura.edu.au/help-research/subscribe>
>
> On 4/02/2015 9:35 am, Douglas Greve wrote:
>>
>> Yes, it should be .^
>>
>> On 2/3/15 5:33 PM, Bronwyn Overs wrote:
>>> Hi Doug,
>>>
>>> I am having a problem with the line in Matlab 2014b:
>>> p = 10^-abs(sigmat);
>>> I keep getting the following error:
>>> Error using  ^
>>> Inputs must be a scalar and a square matrix.
>>> To compute elementwise POWER, use POWER (.^)
>>> instead.
>>>
>>> Do you know why this would be?
>>>
>>> Kind regards,
>>>
>>> Bronwyn Overs
>>> Research Assistant
>>>
>>> Neuroscience Research Australia
>>>
>>> Neuroscience Research Australia
>>> Margarete Ainsworth Building
>>> Barker Street Randwick Sydney NSW 2031 Australia
>>> *M* 0411 308 769 *T* +61 2 9399 1883 *F* +61 2 9399 1265
>>>
>>> neura.edu.au <http://neura.edu.au>
>>>
>>> Follow @neuraustralia on twitter 
>>> <https://twitter.com/neuraustralia>Follow NeuRA on facebook 
>>> <https://www.facebook.com/NeuroscienceResearchAustralia>Subscribe to 
>>> the NeuRA Magazine <http://www.neura.edu.au/help-research/subscribe>
>>>
>>> On 4/02/2015 2:22 am, Douglas Greve wrote:
>>>>
>>>> There is not a way to do it from the command line. You can do it in 
>>>> matlab, something like
>>>>
>>>> sig = MRIread('sig.mgh');
>>>> sigmat = fast_vol2mat(sig);
>>>> p = 10^-abs(sigmat);
>>>> fdr = .05;
>>>> pthresh = fast_fdrthresh(p,fdr);
>>>> ind = find(p < pthresh); % This will be a list of ROI indices that 
>>>> survive FDR
>>>>
>>>> doug
>>>>
>>>> On 2/2/15 10:26 PM, Bronwyn Overs wrote:
>>>>> Hi Doug,
>>>>>
>>>>> That makes perfect sense. Just one more thing then, how do you 
>>>>> conduct an FDR via the command line for an ROI mri_glmfit analysis?
>>>>>
>>>>> Kind regards,
>>>>>
>>>>> Bronwyn Overs
>>>>> Research Assistant
>>>>>
>>>>> Neuroscience Research Australia
>>>>>
>>>>> Neuroscience Research Australia
>>>>> Margarete Ainsworth Building
>>>>> Barker Street Randwick Sydney NSW 2031 Australia
>>>>> *M* 0411 308 769 *T* +61 2 9399 1883 *F* +61 2 9399 1265
>>>>>
>>>>> neura.edu.au <http://neura.edu.au>
>>>>>
>>>>> Follow @neuraustralia on twitter 
>>>>> <https://twitter.com/neuraustralia>Follow NeuRA on facebook 
>>>>> <https://www.facebook.com/NeuroscienceResearchAustralia>Subscribe 
>>>>> to the NeuRA Magazine 
>>>>> <http://www.neura.edu.au/help-research/subscribe>
>>>>>
>>>>> On 3/02/2015 2:00 pm, Douglas Greve wrote:
>>>>>>
>>>>>> This is not something you would run the MC sim on because there 
>>>>>> is no clustering, it is just a list of ROIs with their p-values. 
>>>>>> The p-values are uncorrected. You can do bonferoni correction 
>>>>>> across all the ROIs (or just the ones you are interested in). You 
>>>>>> could do FDR too.
>>>>>>
>>>>>> doug
>>>>>>
>>>>>>
>>>>>> On 2/2/15 9:39 PM, Bronwyn Overs wrote:
>>>>>>> Thanks Doug, that worked well.
>>>>>>>
>>>>>>> However, is it possible to run a monte-carlo simulation with 
>>>>>>> this GLM ROI analysis? I attempted to run it using the following 
>>>>>>> command...
>>>>>>> mri_glmfit-sim --glmdir 
>>>>>>> DesikanROIAnal_case-control.thick.lh.glmdir --cache 1.3 abs 
>>>>>>> --cwpvalthresh  0.05 --2spaces
>>>>>>> and received the following error:
>>>>>>> ERROR: could not determine file for 
>>>>>>> DesikanROIAnal_case-control.thick.lh.glmdir/mask
>>>>>>>
>>>>>>> Kind regards,
>>>>>>>
>>>>>>> Bronwyn Overs
>>>>>>> Research Assistant
>>>>>>>
>>>>>>> Neuroscience Research Australia
>>>>>>>
>>>>>>> Neuroscience Research Australia
>>>>>>> Margarete Ainsworth Building
>>>>>>> Barker Street Randwick Sydney NSW 2031 Australia
>>>>>>> *M* 0411 308 769 *T* +61 2 9399 1883 *F* +61 2 9399 1265
>>>>>>>
>>>>>>> neura.edu.au <http://neura.edu.au>
>>>>>>>
>>>>>>> Follow @neuraustralia on twitter 
>>>>>>> <https://twitter.com/neuraustralia>Follow NeuRA on facebook 
>>>>>>> <https://www.facebook.com/NeuroscienceResearchAustralia>Subscribe to 
>>>>>>> the NeuRA Magazine 
>>>>>>> <http://www.neura.edu.au/help-research/subscribe>
>>>>>>>
>>>>>>> On 3/02/2015 11:03 am, Douglas Greve wrote:
>>>>>>>>
>>>>>>>> Even easier. Run aparcstats2table, then run mri_glmfit passing 
>>>>>>>> the output of aparcstats2table with --table (instead of --y). 
>>>>>>>> There's something on the wiki about it, also look for the ROI 
>>>>>>>> tutorial.
>>>>>>>> doug
>>>>>>>>
>>>>>>>>
>>>>>>>> On 2/2/15 6:20 PM, Bronwyn Overs wrote:
>>>>>>>>> Hi Doug,
>>>>>>>>>
>>>>>>>>> I am not sure how to run an ROI analysis using mri_glmfit. Is 
>>>>>>>>> there a wiki page detailing this method (I was unable to find 
>>>>>>>>> one)? Is the first step to map lh.aparc.label and 
>>>>>>>>> rh.aparc.label from fsaverage to each of my individual 
>>>>>>>>> subjects using mri_label2label? When I do so and then view the 
>>>>>>>>> mapped label for an individual subject in freeview, it appears 
>>>>>>>>> to be a continuous label for all of the parcellated regions 
>>>>>>>>> combined. Is this correct?
>>>>>>>>>
>>>>>>>>> Kind regards,
>>>>>>>>>
>>>>>>>>> Bronwyn Overs
>>>>>>>>> Research Assistant
>>>>>>>>>
>>>>>>>>> Neuroscience Research Australia
>>>>>>>>>
>>>>>>>>> Neuroscience Research Australia
>>>>>>>>> Margarete Ainsworth Building
>>>>>>>>> Barker Street Randwick Sydney NSW 2031 Australia
>>>>>>>>> *M* 0411 308 769 *T* +61 2 9399 1883 *F* +61 2 9399 1265
>>>>>>>>>
>>>>>>>>> neura.edu.au <http://neura.edu.au>
>>>>>>>>>
>>>>>>>>> Follow @neuraustralia on twitter 
>>>>>>>>> <https://twitter.com/neuraustralia>Follow NeuRA on facebook 
>>>>>>>>> <https://www.facebook.com/NeuroscienceResearchAustralia>Subscribe 
>>>>>>>>> to the NeuRA Magazine 
>>>>>>>>> <http://www.neura.edu.au/help-research/subscribe>
>>>>>>>>>
>>>>>>>>> On 3/02/2015 3:31 am, Douglas Greve wrote:
>>>>>>>>>>
>>>>>>>>>> First, I would run the ROI analysis in mri_glmfit to see if 
>>>>>>>>>> you get the same results as in SPSS. In the handfull of these 
>>>>>>>>>> cases, no one has been able to correctly replicate the FS 
>>>>>>>>>> design matrix in SPSS, so I suspect that is part of the 
>>>>>>>>>> discrepancy. The other thing is that ROI and vertex-wise 
>>>>>>>>>> analyses are simply different. As an extreme example, if some 
>>>>>>>>>> of the vertices are pos and some are neg  then they would 
>>>>>>>>>> cancel out when you average them in an ROI but individually 
>>>>>>>>>> could be significant at the vertex level. If you analyze the 
>>>>>>>>>> average over the cluster then that should come out as 
>>>>>>>>>> significant.
>>>>>>>>>>
>>>>>>>>>> doug
>>>>>>>>>>
>>>>>>>>>>
>>>>>>>>>> On 2/1/15 11:36 PM, Bronwyn Overs wrote:
>>>>>>>>>>> Dear FreeSurfer Mailing List,
>>>>>>>>>>>
>>>>>>>>>>> I have a sample of schizophrenia and control subjects for 
>>>>>>>>>>> whom I have run a case-control analysis of cortical 
>>>>>>>>>>> thickness using two separate methods (GLM vertex-wise 
>>>>>>>>>>> analysis in freesurfer, repeated measures ANCOVA analysis of 
>>>>>>>>>>> parcellated data in SPSS). However, for each methods of 
>>>>>>>>>>> analysis I am getting extremely different results. For the 
>>>>>>>>>>> GLM in Freesurfer I have only 1 small cluster in the frontal 
>>>>>>>>>>> lobe that differs between cases and controls (controlling 
>>>>>>>>>>> for all other IVs, FWMH = 10mm, cluster-forming threshold= 
>>>>>>>>>>> .05, cluster-wise pval=.05), while for the ANCOVA method all 
>>>>>>>>>>> but 8 of the parcellated regions differ significantly 
>>>>>>>>>>> between groups (p<.05). For both methods I have used the 
>>>>>>>>>>> same model of predictors (independent variables = gender, 
>>>>>>>>>>> group, scanning site; covariate = age) and exactly the same 
>>>>>>>>>>> sample of participants. I have also replicated the GLM 
>>>>>>>>>>> analysis using the QDEC GUI to ensure that I had no made any 
>>>>>>>>>>> mistakes.
>>>>>>>>>>>
>>>>>>>>>>> Can you provide any insight into why I would be seeing such 
>>>>>>>>>>> different results for each method using the same data set? 
>>>>>>>>>>> My findings using the ANCOVA analysis make much more sense 
>>>>>>>>>>> to me, given previous findings of reduced cortical thickness 
>>>>>>>>>>> in schizophrenia subjects. I was surprised not to find the 
>>>>>>>>>>> same pattern of effects using the GLM analysis.
>>>>>>>>>>> -- 
>>>>>>>>>>>
>>>>>>>>>>> Kind regards,
>>>>>>>>>>>
>>>>>>>>>>> Bronwyn Overs
>>>>>>>>>>> Research Assistant
>>>>>>>>>>>
>>>>>>>>>>> Neuroscience Research Australia
>>>>>>>>>>>
>>>>>>>>>>> Neuroscience Research Australia
>>>>>>>>>>> Margarete Ainsworth Building
>>>>>>>>>>> Barker Street Randwick Sydney NSW 2031 Australia
>>>>>>>>>>> *M* 0411 308 769 *T* +61 2 9399 1883 *F* +61 2 9399 1265
>>>>>>>>>>>
>>>>>>>>>>> neura.edu.au <http://neura.edu.au>
>>>>>>>>>>>
>>>>>>>>>>> Follow @neuraustralia on twitter 
>>>>>>>>>>> <https://twitter.com/neuraustralia>Follow NeuRA on facebook 
>>>>>>>>>>> <https://www.facebook.com/NeuroscienceResearchAustralia>Subscribe 
>>>>>>>>>>> to the NeuRA Magazine 
>>>>>>>>>>> <http://www.neura.edu.au/help-research/subscribe>
>>>>>>>>>>>
>>>>>>>>>>>
>>>>>>>>>>>
>>>>>>>>>>> _______________________________________________
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>>>>>>>>>>> Freesurfer@nmr.mgh.harvard.edu
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>>>>>>>>>>
>>>>>>>>>>
>>>>>>>>>>
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-- 
Douglas N. Greve, Ph.D.
MGH-NMR Center
gr...@nmr.mgh.harvard.edu
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