Hi,
I'm sorry for what seems like a trivial question. I couldn't find this
answer in the tutorials or old archive.
I have statistical data in the surface that I have thresholded and
binarized to form a mask. I can load the mask as an overlay in
tksurfer. My understanding is that you need to tur
Hi,
I have been given data that I need to put in a specific format so that
it's useable to me. I know how to use mri_convert to convert between
analyze and nifti. However, I need one file per run, whereas this
data comes such that every frame is a separate analyze file. How do I
combine them?
Th
I get the message "ReadAnalyzeHeader: unsupported data type 132."
On 12/2/10, Douglas N Greve wrote:
> Try
>
> mri_concat *.img --o f.nii
>
> doug
>
> Rita Loiotile wrote:
>> Hi,
>> I have been given data that I need to put in a specific format so tha
ke we don't read it. You can try the FSL tools.
>
> doug
>
> Rita Loiotile wrote:
>> I get the message "ReadAnalyzeHeader: unsupported data type 132."
>>
>> On 12/2/10, Douglas N Greve wrote:
>>
>>> Try
>>>
>>> mri_conca
For a series of nifti fMRI images does it matter in what order I list
the images for my input? Or does MRI_concat get the time series info
from the files themselves?
Sent from my iPhone
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anyone have it saved anywhere?
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The information in this e-mail is intended only for the person to whom it is
addressed. If you believe
If my BOLD scan has 30 slices in "interleaved" series, can I assume
the slice order is 1,3,5,7,9...29,2,4,6,8..30? In other words,
1:2:30,2:2:30?
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Hi,
How can I tell what the tag-control order of collection was for my ASL
images? They were all acquired in Bay 3. I can get you other
parameters if you need...
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For an odd number of slices- e.g. 45- would it just be
1,3,5,...,45,2,4,...,44 for the Siemens default?
On 2/9/11, Douglas N Greve wrote:
> For Siemens with an even number of slices, it is generally
> 2,4,6,..30,1,3,...29. This changes if there is an odd number of slices.
>
> d