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Hi,

I would start by reading the randomise manual carefully to make sure  
you understand the different files output by randomise, then have a  
careful look at these in FSLView to make sure that you are actually  
getting significant results (>0.95 in the _corrp file). You can  
extract location information about significant clusters using the  
"cluster" program.

Cheers.



On 27 Mar 2009, at 18:05, Yapeng WANG wrote:

> Hi TBSS experts,
> I used TBSS to analysize my DTI data and got TBSS stat. results.  
> Right now I'd like to
> present or extract FA values in a standard space (say MNI 152) with  
> a .txt or excel file
> and correlate FA values with behavioral results. But I do not how to  
> do this.
>
> I tried to do that based on Gwenaelle's suggestion. S/he told me I  
> can run the following
> scripts:
>
> 1) fslmaths my_tbss_results_corrp.nii.gz -thr 0.95 -bin  
> my_significant_results_mask
>
> then:
>
> 2) fslmeants -i all_FA_skeletonised -m my_significant_results_mask -o
> my_significant_results.txt
>
> After I run these two scripts, I got 2 files:  
> my_significant_results_mask. nii.gz and my_significant_results. txt.
>
> In the .txt file, when I run my tbss__results_corrp.nii.gz, the .txt  
> file shows six 0s in a
> column; and when I run my tbss_results.nii.gz, the .txt file shows  
> six numerical values
> ranged from .4000 to .7000. So I guess they are  FA values that I  
> expect, but there are
> no standard coordinates.
> Can anyone tell me how to know the standard coordinate corresponding  
> a specific FA
> value? Ideally, I'd like to know the FA values and corresponding  
> standard coordinates
> from two groups of our subjects. Thank you!
> yp
>


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Stephen M. Smith, Professor of Biomedical Engineering
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