BrainVISA

I kew that in your last version, the dicom reader did'nt work. I wanted to try if it was also the case in the new version (4). But when I want to select files (.dcm), I have to select them manually one by one...!!!!! So : 1. Does the dicom reader work? 2. Can we do multiple selection? Thank you very...

Ok, the 2nd way seems to work!!! :) I just have this message : Morphometry statistics running config : /tmp/bv_293629.cfg Gyrus cliques should have 1 vertex, 2 found here. clique label: Temporal-Middle_left Gyrus cliques should have 1 vertex, 2 found here. clique label: Frontal-Middle_left Process M...

Hello Denis, Yes, I'm talking about the mutual information rigid registration process. It was what I did at the beginning, but the problem is that I would like (for the fiber tracking) define some ROI. And I don't know on each image I have to do that : ideally i would like to define the ROI on the T...

Hello (again!),

I would like to do a registration on two images : the reference is the RGB eigenvector and the source the T1 RMI.
The problem is that I don't find what I have to write in source_to_reference and reference_to_source...

What do I have to choose?

Thank you very much,
Aurélie.

Hello, I tried to follow your advises, but : 1. Even if, I succeded to show the gyrus graph, it seems there is a problem with the display. At the beginning, the image seems to be good, but when we want to rework it (for example to make a zoom) the image looks very bad...! First image : show_gyrus.pn...

Hello, I tried do do what you said but I met some problems for each way you adviced... 1. I can see the field with the "giry graph" buut when I want to open it, it is impossible. How can I open it? Do I have to launch it with anatomist separetely? (the "show" button doesn't work....

Thank you for your reply : I had these messages : Warning: wrong filename_base in graph, trying to fix it Not able to close the projected connnected component, but I continue. Not able to close the projected connnected component, but I continue. Warning: wrong filename_base in graph, trying to fix i...

Hello,

I posted more recent message and had an answer but not for this one.
Could you help me about my fiber tracking please??

Thanks a lot!

Aurely1310

Hi, I tried to fill in manually each field ("old process"), but it was impossible to fill in "left_white_sulci", "right_white_sulci", "left_white_giry_volume" and "right_white_giry_volume". May be there is an operation that I have to do before to lau...

Hello, Thank you for your reply. It would be ideally great.... It was exactly what I wanted to do but... i tried to launch the "old" "gyri parcellation" but nothing happened : After 1s, I've got the message "operation succeded (1s)". So it doesn't seem normal!!! How can...

Hello,

I'm sorry to post again, but it would be really great if I could have a reply...

Thank you very much,
aurely1310

Hello, I would like to know the volume of different gyri. For that I ran the parametrisation of cortical surface pipeline. The operation succeeded and all seems to be good. After that, to have the volume, I tried to launch the surface analysis pipeline. But I don't know how to fill in the field &quo...

Hello, 1. Thank you for fast replying. For the fiber tracking I used q-ball (DTI doesn't interest me). Why are the results so bad? Where is my mistake? 2. For the pipeline I will open a new post. 3. And for HBM, I'll not personnaly be here, but my boss will go (probably with my computer). Who can he...

Hello,

I'm sorry to write again, but could you help me please, about the previous posts?

And another question : will someone of your team be on the HBM conference (Barcelone) next week?

Thank you very much,
Aurely1310

Hello,

I'm sorry to write again, but could you help me please, about the previous posts?

And another question : will someone of your team be on the HBM conference (Barcelone) next week?

Thank you very much,
Aurely1310