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HI - yes you should just use the finalPBVC.
Cheers.


On 12 Dec 2013, at 21:19, Amlish Munir <[log in to unmask]> wrote:

> Hi folks,
> 
> I have just started working with the Siena package to quantify atrophy.  As a test, I've run siena on the same image, as well as a slightly modified image where I've removed some white matter.  
> 
> Same image for time point 1 and time point 2:
> --------------------------------------------------------
> - Curiously, when Siena was run on the same image, the atrophy measurements for A to B and B to A are non-zero and the same sign (not correcting for direction) meaning A to B has growth and B to A has growth .  While this results in a total atrophy of 0 ( AtoB + -1*(BtoA) ), I can't understand why a constant is being introduced when the images are the same.  Does the algorithm introduce a constant offset and as a result we should only ever consider the final PBVC?
> 
> /usr/local/fsl/bin/fast   B_halfwayto_A_brain > B_halfwayto_A_brain.vol 2>&1
> finding brain edges
> finding flow
> AREA  242168 mm^2
> VOLC  1064.67 mm^3
> RATIO 0.00439641 mm
> PBVC  0.170188 %
> 
> /usr/local/fsl/bin/fast   A_halfwayto_B_brain > A_halfwayto_B_brain.vol 2>&1
> finding brain edges
> finding flow
> AREA  242168 mm^2
> VOLC  1064.67 mm^3
> RATIO 0.00439641 mm
> PBVC  0.170188 %
> 
> finalPBVC 0 %
> 
> 
> Same base image for time point 1 and 2 but some white matter from 2 is manually removed:
> ----------------------------------------------------------------------------------------------------------------
> - Results seem sensible with atrophy being recorded appropriately around the constructed lesion but the lesion does bias  the registration slightly leading to edge differences.
> 
> Thanks for your help.
> 
> Amlish


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