Hi hcp-users,

I am trying to use MGH diffusion data for tractography analysis. In this 
dataset, 4 shells (bvals = 1k, 3k, 5k, 10k s/mm2) were concatenated (552 
volumes in total). My questions are:

1) Do I have to separate the 4 shells for further analysis (tractography)? If 
so, how can I separate them?

2) The MGH diffusion data is nifti format. I may also use this dataset at the 
other platform. How can I convert the nifti into nrrd format please?

Thank you very much.
Zhenrui 


--
Zhenrui Chen, MD (aka Jerry)
Research Fellow
Department of Neurosurgery
Brigham and Women's Hospital
75 Francis Street, Boston, MA 02115




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