Use of tck2fixel, fixel2sh and tckmap

Dear Mrtrix experts,

From a fiber bundle (the cingulum), I would like to extract the FOD lobes that contributed to the construction of this bundle from the original FOD used to build the bundle. In order to do this, I used the following commands :

dwi2fod csd dwi.nii.gz response.tst FOD.nii.gz -grad grad.txt
fod2fixel FOD.nii.gz -peak_amp amp.nii.gz -afd afd.nii.gz fixel_from_fod -mask cingulum_binarymask.nii.gz
tck2fixel cingulum.tck fixel_from_fod fixel_from_tck fixel_from_tck.nii.gz
fixel2sh fixel_from_tck/directions.mif FOD_from_fixel_from_tck.nii.gz

When visualizing FOD_from_fixel_from_tck.nii.gz, I have something quite suprising with very small FOD lobes where the bundle seems to be the most dense.

Looking on ways to solve my problem, I discovered the command tckmap which gave me the result I was expercting from the command fixel2sh :

tckmap cingulum.tck TOD_from_tck.nii.gz -templade dwi.nii.gz -lmax 6

I guess I must be misunderstanding something with the use of the fixels but why do I get very small FOD lobes where the bundle seems really dense ?

Thank you in advance for your help,

Hi Louise,

The issue you’re highlighting here is precisely what SIFT / SIFT2 were designed to address: using standard streamlines-based tractography approaches, there is no simple relationship between streamlines density and ‘apparent’ fibre density (e.g. as observed from the FOD). I recommend you have a look through the relevant papers (particularly the original SIFT paper) to understand why that is. The fact that you’re representing these as fixels is broadly unrelated to that.

More recently, @rsmith wrote a whole paper on the topic, which is currently available as a pre-print. I recommend you have a look in there for more detailed look into the issues.