Re: [caret-users] doubt regarding fiducial mapping

2015-08-25 Thread john
> Hello Donna,
 Thank you for your response. I think now the functional and anatomical is
aligned properly once i do a reslicing(in SPM) of functional and aligning
it in par with anatomical image parameters in caret.
Thank you for your kind help,
john




Hi John,
>
> My trials with your data are detailed here:
>
>> http://brainmap.wustl.edu/pub/donna/IN/JOHN/align.html
>> login pub
>> password download
>
>
> I suspect there are better ways of dealing with oblique data, and I hope
> others will chime in if they have alternative suggestions.  (They don't
> have to be "better" -- just offering other perspectives, even.)  This was
> the best I could do with the information I have.
>
> Donna
>
>
> On Aug 20, 2015, at 12:43 PM, j...@nbrc.ac.in wrote:
>
>>> Hi Donna,
>> There were no steps that involved any de-obliquing, flipped, or
>>> shifted, AC-centered  "LPI" orientation.
>> i loaded the image, anatomical and in volume attributes I checked the
>> orientation, put the crossline at AC after shifting the image manually
>> through co ordinate values, and selected the option to keep AC position
>> as crossline position in main window. after this i gave coordinates of
>> posterior comm, and middle fissure and checked voxel size etc...
>> then i saved it as AC centered image.
>>
>>
>>
>> Hi John,
>>>
>>> Those tweaks were very helpful.  I looked at the volumes with the
>>> surface
>>> overlaid, and here's what I found:
>>>
>>> http://brainmap.wustl.edu/pub/donna/IN/JOHN/align.html
>>> login pub
>>> password download
>>>
>>> I don't trust Caret to handle oblique volumes properly.  Quoting the
>>> link
>>> above, "Can you go back through the history of this volume's processing
>>> --
>>> specifically what happened to generate anatomical_ac_centered.hdr from
>>> anatomical_image.hdr? Were there steps the de-obliqued, flipped, or
>>> shifted the anatomical to get it AC-centered and probably in "LPI"
>>> orientation, as Caret required to segment?"
>>>
>>> Donna
>>>
>>>
>>> On Aug 20, 2015, at 1:02 AM, j...@nbrc.ac.in wrote:
>>>
 Hello Donna,
 I've made the necessary changes and uploaded the file.

 john.



 If you can find your *.params file, then don't worry about the find
> command, which was intended to help you locate it if you did not know
> its
> name/location already.
>
> I looked at your dataset, and you must do two things to help me help
> you:
>
> * Remove the spaces from the filenames.  Replace them with _
> characters.
> When I try to read, move, or otherwise manipulate these files, the
> spaces
> are misinterpreted by the Linux shell as separate arguments.
>
> * Add the *.params file.
>
> After you've made those changes, rename the directory john_renamed.
> Then
> zip it and upload it.  I'll do my best to solve it.
>
>
> On Aug 19, 2015, at 1:23 AM, j...@nbrc.ac.in wrote:
>
>>> Hello Donna,
>>
>> 1.I ve tried taking the XYZ min values from .PARAMS file and
>> transformed
>> the overlay. This appears very subjective and error prone.
>>
>> 2. "Do this in your subject directory:
>>>
>>> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
>> "
>>
>> I am not sure i understood this step properly
>>
>>
>> I am unable to coregister the functional image and anatomical image
>> properly.
>> I am sorry to trouble you again , but it would be great if you can
>> take
>> a
>> look at the dataset again, which i have uploaded in a folder " data
>> from
>> john.zip" at http://pulvinar.wustl.edu/cgi-bin/upload.cgi
>>
>> I doubt now that there is some issue within the procedure that we
>> follow
>> in doing the analysis. So it would be best if you can
>> check/reanalyse
>> the
>> dataset from very initial step itself.
>>
>> PS:
>> -anatomical image.hdr\img---unaltered structural T1 image.
>> -functional.hdr\imgbasic SPM8  T2*image which is to be mapped
>>
>> Thank you.
>>
>>
>>
>>
>> On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:
>>>
 Hello Donna,
 Thank you for your reply.
 Two doubts i have
 1. why even after loading metric as primary overlay it is not
 getting
 'selectable' here in functional view (see attachment "capture")?
>>>
>>> The metric is a vertex-intensity mapping.  It is not the volume.
>>> You
>>> can
>>> load the volume that was mapped using File: Open Data File: Volume
>>> Functional files.  Then it will be selectable when you map to
>>> loaded
>>> volume.  Or you can simply map to file on disk without loading.
>>> But
>>> it
>>> is
>>> not a bad idea to load the volume, too, to make sure everything
>>> aligns
>>> properly:  Functional with surface is the important one, but the
>>> anatomical volume is

Re: [caret-users] doubt regarding fiducial mapping

2015-08-21 Thread Donna Dierker
Hi John,

My trials with your data are detailed here:

> http://brainmap.wustl.edu/pub/donna/IN/JOHN/align.html
> login pub
> password download


I suspect there are better ways of dealing with oblique data, and I hope others 
will chime in if they have alternative suggestions.  (They don't have to be 
"better" -- just offering other perspectives, even.)  This was the best I could 
do with the information I have.

Donna


On Aug 20, 2015, at 12:43 PM, j...@nbrc.ac.in wrote:

>> Hi Donna,
> There were no steps that involved any de-obliquing, flipped, or
>> shifted, AC-centered  "LPI" orientation.
> i loaded the image, anatomical and in volume attributes I checked the
> orientation, put the crossline at AC after shifting the image manually
> through co ordinate values, and selected the option to keep AC position
> as crossline position in main window. after this i gave coordinates of
> posterior comm, and middle fissure and checked voxel size etc...
> then i saved it as AC centered image.
> 
> 
> 
> Hi John,
>> 
>> Those tweaks were very helpful.  I looked at the volumes with the surface
>> overlaid, and here's what I found:
>> 
>> http://brainmap.wustl.edu/pub/donna/IN/JOHN/align.html
>> login pub
>> password download
>> 
>> I don't trust Caret to handle oblique volumes properly.  Quoting the link
>> above, "Can you go back through the history of this volume's processing --
>> specifically what happened to generate anatomical_ac_centered.hdr from
>> anatomical_image.hdr? Were there steps the de-obliqued, flipped, or
>> shifted the anatomical to get it AC-centered and probably in "LPI"
>> orientation, as Caret required to segment?"
>> 
>> Donna
>> 
>> 
>> On Aug 20, 2015, at 1:02 AM, j...@nbrc.ac.in wrote:
>> 
>>> Hello Donna,
>>> I've made the necessary changes and uploaded the file.
>>> 
>>> john.
>>> 
>>> 
>>> 
>>> If you can find your *.params file, then don't worry about the find
 command, which was intended to help you locate it if you did not know
 its
 name/location already.
 
 I looked at your dataset, and you must do two things to help me help
 you:
 
 * Remove the spaces from the filenames.  Replace them with _
 characters.
 When I try to read, move, or otherwise manipulate these files, the
 spaces
 are misinterpreted by the Linux shell as separate arguments.
 
 * Add the *.params file.
 
 After you've made those changes, rename the directory john_renamed.
 Then
 zip it and upload it.  I'll do my best to solve it.
 
 
 On Aug 19, 2015, at 1:23 AM, j...@nbrc.ac.in wrote:
 
>> Hello Donna,
> 
> 1.I ve tried taking the XYZ min values from .PARAMS file and
> transformed
> the overlay. This appears very subjective and error prone.
> 
> 2. "Do this in your subject directory:
>> 
>> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
> "
> 
> I am not sure i understood this step properly
> 
> 
> I am unable to coregister the functional image and anatomical image
> properly.
> I am sorry to trouble you again , but it would be great if you can
> take
> a
> look at the dataset again, which i have uploaded in a folder " data
> from
> john.zip" at http://pulvinar.wustl.edu/cgi-bin/upload.cgi
> 
> I doubt now that there is some issue within the procedure that we
> follow
> in doing the analysis. So it would be best if you can check/reanalyse
> the
> dataset from very initial step itself.
> 
> PS:
> -anatomical image.hdr\img---unaltered structural T1 image.
> -functional.hdr\imgbasic SPM8  T2*image which is to be mapped
> 
> Thank you.
> 
> 
> 
> 
> On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:
>> 
>>> Hello Donna,
>>> Thank you for your reply.
>>> Two doubts i have
>>> 1. why even after loading metric as primary overlay it is not
>>> getting
>>> 'selectable' here in functional view (see attachment "capture")?
>> 
>> The metric is a vertex-intensity mapping.  It is not the volume.  You
>> can
>> load the volume that was mapped using File: Open Data File: Volume
>> Functional files.  Then it will be selectable when you map to loaded
>> volume.  Or you can simply map to file on disk without loading.  But
>> it
>> is
>> not a bad idea to load the volume, too, to make sure everything
>> aligns
>> properly:  Functional with surface is the important one, but the
>> anatomical volume is the link between functional and surface (i.e.,
>> how
>> they get aligned).
>> 
>>> 2. what is the meaning of this error message (attachment 2), which
>>> appears
>>> on selecting the functional volumes?
>> 
>> Again, the funky file naming of two of the volume files (e.g., space,
>> parentheses, leading dashes) impedes my ability to check them
>> quickly.
>

Re: [caret-users] doubt regarding fiducial mapping

2015-08-20 Thread john
> Hi Donna,
There were no steps that involved any de-obliquing, flipped, or
> shifted, AC-centered  "LPI" orientation.
 i loaded the image, anatomical and in volume attributes I checked the
orientation, put the crossline at AC after shifting the image manually
through co ordinate values, and selected the option to keep AC position
as crossline position in main window. after this i gave coordinates of
posterior comm, and middle fissure and checked voxel size etc...
 then i saved it as AC centered image.







Hi John,
>
> Those tweaks were very helpful.  I looked at the volumes with the surface
> overlaid, and here's what I found:
>
> http://brainmap.wustl.edu/pub/donna/IN/JOHN/align.html
> login pub
> password download
>
> I don't trust Caret to handle oblique volumes properly.  Quoting the link
> above, "Can you go back through the history of this volume's processing --
> specifically what happened to generate anatomical_ac_centered.hdr from
> anatomical_image.hdr? Were there steps the de-obliqued, flipped, or
> shifted the anatomical to get it AC-centered and probably in "LPI"
> orientation, as Caret required to segment?"
>
> Donna
>
>
> On Aug 20, 2015, at 1:02 AM, j...@nbrc.ac.in wrote:
>
>> Hello Donna,
>> I've made the necessary changes and uploaded the file.
>>
>> john.
>>
>>
>>
>> If you can find your *.params file, then don't worry about the find
>>> command, which was intended to help you locate it if you did not know
>>> its
>>> name/location already.
>>>
>>> I looked at your dataset, and you must do two things to help me help
>>> you:
>>>
>>> * Remove the spaces from the filenames.  Replace them with _
>>> characters.
>>> When I try to read, move, or otherwise manipulate these files, the
>>> spaces
>>> are misinterpreted by the Linux shell as separate arguments.
>>>
>>> * Add the *.params file.
>>>
>>> After you've made those changes, rename the directory john_renamed.
>>> Then
>>> zip it and upload it.  I'll do my best to solve it.
>>>
>>>
>>> On Aug 19, 2015, at 1:23 AM, j...@nbrc.ac.in wrote:
>>>
> Hello Donna,

 1.I ve tried taking the XYZ min values from .PARAMS file and
 transformed
 the overlay. This appears very subjective and error prone.

 2. "Do this in your subject directory:
>
> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
 "

 I am not sure i understood this step properly


 I am unable to coregister the functional image and anatomical image
 properly.
 I am sorry to trouble you again , but it would be great if you can
 take
 a
 look at the dataset again, which i have uploaded in a folder " data
 from
 john.zip" at http://pulvinar.wustl.edu/cgi-bin/upload.cgi

 I doubt now that there is some issue within the procedure that we
 follow
 in doing the analysis. So it would be best if you can check/reanalyse
 the
 dataset from very initial step itself.

 PS:
 -anatomical image.hdr\img---unaltered structural T1 image.
 -functional.hdr\imgbasic SPM8  T2*image which is to be mapped

 Thank you.




 On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:
>
>> Hello Donna,
>> Thank you for your reply.
>> Two doubts i have
>> 1. why even after loading metric as primary overlay it is not
>> getting
>> 'selectable' here in functional view (see attachment "capture")?
>
> The metric is a vertex-intensity mapping.  It is not the volume.  You
> can
> load the volume that was mapped using File: Open Data File: Volume
> Functional files.  Then it will be selectable when you map to loaded
> volume.  Or you can simply map to file on disk without loading.  But
> it
> is
> not a bad idea to load the volume, too, to make sure everything
> aligns
> properly:  Functional with surface is the important one, but the
> anatomical volume is the link between functional and surface (i.e.,
> how
> they get aligned).
>
>> 2. what is the meaning of this error message (attachment 2), which
>> appears
>> on selecting the functional volumes?
>
> Again, the funky file naming of two of the volume files (e.g., space,
> parentheses, leading dashes) impedes my ability to check them
> quickly.
> But the whole brain anatomical does appear to be a NIfTI volume,
> rather
> than just an Analyze .hdr file.  I loaded it as a functional volume,
> and
> then tried to map it to your surface.  I got the same result as
> trying
> to
> map it from disk (clicking OK on the stickup you captured).
>
> That warning never got removed after support for nifti .hdr/.img
> pairs
> was
> added, but based on my getting the same results using the two paths
> mentioned above, I think you will solve your problem when you solve
> the
> misalignment between your cropped volume and the whole brain
>

Re: [caret-users] doubt regarding fiducial mapping

2015-08-20 Thread Donna Dierker
Hi John,

Those tweaks were very helpful.  I looked at the volumes with the surface 
overlaid, and here's what I found:

http://brainmap.wustl.edu/pub/donna/IN/JOHN/align.html
login pub
password download

I don't trust Caret to handle oblique volumes properly.  Quoting the link 
above, "Can you go back through the history of this volume's processing -- 
specifically what happened to generate anatomical_ac_centered.hdr from 
anatomical_image.hdr? Were there steps the de-obliqued, flipped, or shifted the 
anatomical to get it AC-centered and probably in "LPI" orientation, as Caret 
required to segment?"

Donna


On Aug 20, 2015, at 1:02 AM, j...@nbrc.ac.in wrote:

> Hello Donna,
> I've made the necessary changes and uploaded the file.
> 
> john.
> 
> 
> 
> If you can find your *.params file, then don't worry about the find
>> command, which was intended to help you locate it if you did not know its
>> name/location already.
>> 
>> I looked at your dataset, and you must do two things to help me help you:
>> 
>> * Remove the spaces from the filenames.  Replace them with _ characters.
>> When I try to read, move, or otherwise manipulate these files, the spaces
>> are misinterpreted by the Linux shell as separate arguments.
>> 
>> * Add the *.params file.
>> 
>> After you've made those changes, rename the directory john_renamed.  Then
>> zip it and upload it.  I'll do my best to solve it.
>> 
>> 
>> On Aug 19, 2015, at 1:23 AM, j...@nbrc.ac.in wrote:
>> 
 Hello Donna,
>>> 
>>> 1.I ve tried taking the XYZ min values from .PARAMS file and transformed
>>> the overlay. This appears very subjective and error prone.
>>> 
>>> 2. "Do this in your subject directory:
 
 find /my/subject/dir -name "*.params" |sort | xargs grep -i min
>>> "
>>> 
>>> I am not sure i understood this step properly
>>> 
>>> 
>>> I am unable to coregister the functional image and anatomical image
>>> properly.
>>> I am sorry to trouble you again , but it would be great if you can take
>>> a
>>> look at the dataset again, which i have uploaded in a folder " data from
>>> john.zip" at http://pulvinar.wustl.edu/cgi-bin/upload.cgi
>>> 
>>> I doubt now that there is some issue within the procedure that we follow
>>> in doing the analysis. So it would be best if you can check/reanalyse
>>> the
>>> dataset from very initial step itself.
>>> 
>>> PS:
>>> -anatomical image.hdr\img---unaltered structural T1 image.
>>> -functional.hdr\imgbasic SPM8  T2*image which is to be mapped
>>> 
>>> Thank you.
>>> 
>>> 
>>> 
>>> 
>>> On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:
 
> Hello Donna,
> Thank you for your reply.
> Two doubts i have
> 1. why even after loading metric as primary overlay it is not getting
> 'selectable' here in functional view (see attachment "capture")?
 
 The metric is a vertex-intensity mapping.  It is not the volume.  You
 can
 load the volume that was mapped using File: Open Data File: Volume
 Functional files.  Then it will be selectable when you map to loaded
 volume.  Or you can simply map to file on disk without loading.  But it
 is
 not a bad idea to load the volume, too, to make sure everything aligns
 properly:  Functional with surface is the important one, but the
 anatomical volume is the link between functional and surface (i.e., how
 they get aligned).
 
> 2. what is the meaning of this error message (attachment 2), which
> appears
> on selecting the functional volumes?
 
 Again, the funky file naming of two of the volume files (e.g., space,
 parentheses, leading dashes) impedes my ability to check them quickly.
 But the whole brain anatomical does appear to be a NIfTI volume, rather
 than just an Analyze .hdr file.  I loaded it as a functional volume,
 and
 then tried to map it to your surface.  I got the same result as trying
 to
 map it from disk (clicking OK on the stickup you captured).
 
 That warning never got removed after support for nifti .hdr/.img pairs
 was
 added, but based on my getting the same results using the two paths
 mentioned above, I think you will solve your problem when you solve the
 misalignment between your cropped volume and the whole brain anatomical
 volume.  Alternatively, shift the surface to meet the whole brain /
 functional volume.
 
 Ideally, get the following loaded and aligned in caret:
 
 * whole brain anatomy volume
 * functional volume overlay
 * surface (probably shifted version of what you have now)
 
 Do this in your subject directory:
 
 find /my/subject/dir -name "*.params" |sort | xargs grep -i min
 
 Capture it to a file if it's a lot.  One of those files has the offset
 you
 need.
 
> thank you.
> 
> 
> Hi John,
>> 
>> Got your upload.  While I couldn't open the cropped volume in caret
>> due
>> to
>> the way it 

Re: [caret-users] doubt regarding fiducial mapping

2015-08-20 Thread john
Hello Donna,
 I've made the necessary changes and uploaded the file.

john.



 If you can find your *.params file, then don't worry about the find
> command, which was intended to help you locate it if you did not know its
> name/location already.
>
> I looked at your dataset, and you must do two things to help me help you:
>
> * Remove the spaces from the filenames.  Replace them with _ characters.
> When I try to read, move, or otherwise manipulate these files, the spaces
> are misinterpreted by the Linux shell as separate arguments.
>
> * Add the *.params file.
>
> After you've made those changes, rename the directory john_renamed.  Then
> zip it and upload it.  I'll do my best to solve it.
>
>
> On Aug 19, 2015, at 1:23 AM, j...@nbrc.ac.in wrote:
>
>>> Hello Donna,
>>
>> 1.I ve tried taking the XYZ min values from .PARAMS file and transformed
>> the overlay. This appears very subjective and error prone.
>>
>> 2. "Do this in your subject directory:
>>>
>>> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
>> "
>>
>> I am not sure i understood this step properly
>>
>>
>> I am unable to coregister the functional image and anatomical image
>> properly.
>> I am sorry to trouble you again , but it would be great if you can take
>> a
>> look at the dataset again, which i have uploaded in a folder " data from
>> john.zip" at http://pulvinar.wustl.edu/cgi-bin/upload.cgi
>>
>> I doubt now that there is some issue within the procedure that we follow
>> in doing the analysis. So it would be best if you can check/reanalyse
>> the
>> dataset from very initial step itself.
>>
>> PS:
>> -anatomical image.hdr\img---unaltered structural T1 image.
>> -functional.hdr\imgbasic SPM8  T2*image which is to be mapped
>>
>> Thank you.
>>
>>
>>
>>
>> On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:
>>>
 Hello Donna,
 Thank you for your reply.
 Two doubts i have
 1. why even after loading metric as primary overlay it is not getting
 'selectable' here in functional view (see attachment "capture")?
>>>
>>> The metric is a vertex-intensity mapping.  It is not the volume.  You
>>> can
>>> load the volume that was mapped using File: Open Data File: Volume
>>> Functional files.  Then it will be selectable when you map to loaded
>>> volume.  Or you can simply map to file on disk without loading.  But it
>>> is
>>> not a bad idea to load the volume, too, to make sure everything aligns
>>> properly:  Functional with surface is the important one, but the
>>> anatomical volume is the link between functional and surface (i.e., how
>>> they get aligned).
>>>
 2. what is the meaning of this error message (attachment 2), which
 appears
 on selecting the functional volumes?
>>>
>>> Again, the funky file naming of two of the volume files (e.g., space,
>>> parentheses, leading dashes) impedes my ability to check them quickly.
>>> But the whole brain anatomical does appear to be a NIfTI volume, rather
>>> than just an Analyze .hdr file.  I loaded it as a functional volume,
>>> and
>>> then tried to map it to your surface.  I got the same result as trying
>>> to
>>> map it from disk (clicking OK on the stickup you captured).
>>>
>>> That warning never got removed after support for nifti .hdr/.img pairs
>>> was
>>> added, but based on my getting the same results using the two paths
>>> mentioned above, I think you will solve your problem when you solve the
>>> misalignment between your cropped volume and the whole brain anatomical
>>> volume.  Alternatively, shift the surface to meet the whole brain /
>>> functional volume.
>>>
>>> Ideally, get the following loaded and aligned in caret:
>>>
>>> * whole brain anatomy volume
>>> * functional volume overlay
>>> * surface (probably shifted version of what you have now)
>>>
>>> Do this in your subject directory:
>>>
>>> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
>>>
>>> Capture it to a file if it's a lot.  One of those files has the offset
>>> you
>>> need.
>>>
 thank you.


 Hi John,
>
> Got your upload.  While I couldn't open the cropped volume in caret
> due
> to
> the way it was named, I was able to view the surface contour over the
> uncropped volume.  See attached capture, which shows an offset.
>
> If you have a SureFit/Caret .params file (not included in the zip),
> it
> might contain the [XYZ]min values from the cropping, which might be
> used
> to either adjust the functional volume's origin, or more likely apply
> an
> affine transform to the surface, to shift it back into alignment with
> the
> whole brain volume.  You don't have to blow away your existing coord;
> just
> rename the shifted version to indicate the offset.  This can be done
> via
> command line or using the Caret: Window: Transformation Matrix
> editor.
> The polarity of the shift (+ or -) depends on whether you're shifting
> the
> volume or su

Re: [caret-users] doubt regarding fiducial mapping

2015-08-19 Thread Donna Dierker
If you can find your *.params file, then don't worry about the find command, 
which was intended to help you locate it if you did not know its name/location 
already.

I looked at your dataset, and you must do two things to help me help you:

* Remove the spaces from the filenames.  Replace them with _ characters.  When 
I try to read, move, or otherwise manipulate these files, the spaces are 
misinterpreted by the Linux shell as separate arguments.

* Add the *.params file.

After you've made those changes, rename the directory john_renamed.  Then zip 
it and upload it.  I'll do my best to solve it.


On Aug 19, 2015, at 1:23 AM, j...@nbrc.ac.in wrote:

>> Hello Donna,
> 
> 1.I ve tried taking the XYZ min values from .PARAMS file and transformed
> the overlay. This appears very subjective and error prone.
> 
> 2. "Do this in your subject directory:
>> 
>> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
> "
> 
> I am not sure i understood this step properly
> 
> 
> I am unable to coregister the functional image and anatomical image properly.
> I am sorry to trouble you again , but it would be great if you can take a
> look at the dataset again, which i have uploaded in a folder " data from
> john.zip" at http://pulvinar.wustl.edu/cgi-bin/upload.cgi
> 
> I doubt now that there is some issue within the procedure that we follow
> in doing the analysis. So it would be best if you can check/reanalyse the
> dataset from very initial step itself.
> 
> PS:
> -anatomical image.hdr\img---unaltered structural T1 image.
> -functional.hdr\imgbasic SPM8  T2*image which is to be mapped
> 
> Thank you.
> 
> 
> 
> 
> On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:
>> 
>>> Hello Donna,
>>> Thank you for your reply.
>>> Two doubts i have
>>> 1. why even after loading metric as primary overlay it is not getting
>>> 'selectable' here in functional view (see attachment "capture")?
>> 
>> The metric is a vertex-intensity mapping.  It is not the volume.  You can
>> load the volume that was mapped using File: Open Data File: Volume
>> Functional files.  Then it will be selectable when you map to loaded
>> volume.  Or you can simply map to file on disk without loading.  But it is
>> not a bad idea to load the volume, too, to make sure everything aligns
>> properly:  Functional with surface is the important one, but the
>> anatomical volume is the link between functional and surface (i.e., how
>> they get aligned).
>> 
>>> 2. what is the meaning of this error message (attachment 2), which
>>> appears
>>> on selecting the functional volumes?
>> 
>> Again, the funky file naming of two of the volume files (e.g., space,
>> parentheses, leading dashes) impedes my ability to check them quickly.
>> But the whole brain anatomical does appear to be a NIfTI volume, rather
>> than just an Analyze .hdr file.  I loaded it as a functional volume, and
>> then tried to map it to your surface.  I got the same result as trying to
>> map it from disk (clicking OK on the stickup you captured).
>> 
>> That warning never got removed after support for nifti .hdr/.img pairs was
>> added, but based on my getting the same results using the two paths
>> mentioned above, I think you will solve your problem when you solve the
>> misalignment between your cropped volume and the whole brain anatomical
>> volume.  Alternatively, shift the surface to meet the whole brain /
>> functional volume.
>> 
>> Ideally, get the following loaded and aligned in caret:
>> 
>> * whole brain anatomy volume
>> * functional volume overlay
>> * surface (probably shifted version of what you have now)
>> 
>> Do this in your subject directory:
>> 
>> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
>> 
>> Capture it to a file if it's a lot.  One of those files has the offset you
>> need.
>> 
>>> thank you.
>>> 
>>> 
>>> Hi John,
 
 Got your upload.  While I couldn't open the cropped volume in caret due
 to
 the way it was named, I was able to view the surface contour over the
 uncropped volume.  See attached capture, which shows an offset.
 
 If you have a SureFit/Caret .params file (not included in the zip), it
 might contain the [XYZ]min values from the cropping, which might be
 used
 to either adjust the functional volume's origin, or more likely apply
 an
 affine transform to the surface, to shift it back into alignment with
 the
 whole brain volume.  You don't have to blow away your existing coord;
 just
 rename the shifted version to indicate the offset.  This can be done
 via
 command line or using the Caret: Window: Transformation Matrix editor.
 The polarity of the shift (+ or -) depends on whether you're shifting
 the
 volume or surface, and I always get confused about it.  Usually I try
 it
 one way; look at the result like the capture below; and if it looks
 worse,
 I try it the other way. ;-)  One of the ways usually does the trick.
>>>

Re: [caret-users] doubt regarding fiducial mapping

2015-08-19 Thread john
> Hello Donna,

1.I ve tried taking the XYZ min values from .PARAMS file and transformed
the overlay. This appears very subjective and error prone.

2. "Do this in your subject directory:
>
> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
"

I am not sure i understood this step properly


I am unable to coregister the functional image and anatomical image properly.
I am sorry to trouble you again , but it would be great if you can take a
look at the dataset again, which i have uploaded in a folder " data from
john.zip" at http://pulvinar.wustl.edu/cgi-bin/upload.cgi

I doubt now that there is some issue within the procedure that we follow
in doing the analysis. So it would be best if you can check/reanalyse the
dataset from very initial step itself.

PS:
-anatomical image.hdr\img---unaltered structural T1 image.
-functional.hdr\imgbasic SPM8  T2*image which is to be mapped

Thank you.




On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:
>
>> Hello Donna,
>> Thank you for your reply.
>> Two doubts i have
>> 1. why even after loading metric as primary overlay it is not getting
>> 'selectable' here in functional view (see attachment "capture")?
>
> The metric is a vertex-intensity mapping.  It is not the volume.  You can
> load the volume that was mapped using File: Open Data File: Volume
> Functional files.  Then it will be selectable when you map to loaded
> volume.  Or you can simply map to file on disk without loading.  But it is
> not a bad idea to load the volume, too, to make sure everything aligns
> properly:  Functional with surface is the important one, but the
> anatomical volume is the link between functional and surface (i.e., how
> they get aligned).
>
>> 2. what is the meaning of this error message (attachment 2), which
>> appears
>> on selecting the functional volumes?
>
> Again, the funky file naming of two of the volume files (e.g., space,
> parentheses, leading dashes) impedes my ability to check them quickly.
> But the whole brain anatomical does appear to be a NIfTI volume, rather
> than just an Analyze .hdr file.  I loaded it as a functional volume, and
> then tried to map it to your surface.  I got the same result as trying to
> map it from disk (clicking OK on the stickup you captured).
>
> That warning never got removed after support for nifti .hdr/.img pairs was
> added, but based on my getting the same results using the two paths
> mentioned above, I think you will solve your problem when you solve the
> misalignment between your cropped volume and the whole brain anatomical
> volume.  Alternatively, shift the surface to meet the whole brain /
> functional volume.
>
> Ideally, get the following loaded and aligned in caret:
>
> * whole brain anatomy volume
> * functional volume overlay
> * surface (probably shifted version of what you have now)
>
> Do this in your subject directory:
>
> find /my/subject/dir -name "*.params" |sort | xargs grep -i min
>
> Capture it to a file if it's a lot.  One of those files has the offset you
> need.
>
>> thank you.
>>
>>
>> Hi John,
>>>
>>> Got your upload.  While I couldn't open the cropped volume in caret due
>>> to
>>> the way it was named, I was able to view the surface contour over the
>>> uncropped volume.  See attached capture, which shows an offset.
>>>
>>> If you have a SureFit/Caret .params file (not included in the zip), it
>>> might contain the [XYZ]min values from the cropping, which might be
>>> used
>>> to either adjust the functional volume's origin, or more likely apply
>>> an
>>> affine transform to the surface, to shift it back into alignment with
>>> the
>>> whole brain volume.  You don't have to blow away your existing coord;
>>> just
>>> rename the shifted version to indicate the offset.  This can be done
>>> via
>>> command line or using the Caret: Window: Transformation Matrix editor.
>>> The polarity of the shift (+ or -) depends on whether you're shifting
>>> the
>>> volume or surface, and I always get confused about it.  Usually I try
>>> it
>>> one way; look at the result like the capture below; and if it looks
>>> worse,
>>> I try it the other way. ;-)  One of the ways usually does the trick.
>>>
>>> Donna
>>>
>>>
>>>
>>> On Aug 12, 2015, at 9:14 AM, Donna Dierker 
>>> wrote:
>>>
 Could you upload your dataset in a zip archive here:

>>>
 http://pulvinar.wustl.edu/cgi-bin/upload.cgi

 Specifically I need:

 * functional volume being mapped
 * anatomical volume with which functional volume aligns
 * anatomical volume used to generate segmentation -- *cropped*
 * fiducial coord file
 * topology file

 I am wondering if the centers of the volumes between the cropped
 volume
 used to generate the surface and the whole brain anatomical volume.


 On Aug 12, 2015, at 1:11 AM, j...@nbrc.ac.in wrote:

>>
>
> Ya, sorry for the incomplete query.
> Our interest is to view and threshold fMRI/voxel correlation data
>>>

Re: [caret-users] doubt regarding fiducial mapping

2015-08-18 Thread Donna Dierker
On Aug 18, 2015, at 2:19 AM, j...@nbrc.ac.in wrote:

> Hello Donna,
> Thank you for your reply.
> Two doubts i have
> 1. why even after loading metric as primary overlay it is not getting
> 'selectable' here in functional view (see attachment "capture")?

The metric is a vertex-intensity mapping.  It is not the volume.  You can load 
the volume that was mapped using File: Open Data File: Volume Functional files. 
 Then it will be selectable when you map to loaded volume.  Or you can simply 
map to file on disk without loading.  But it is not a bad idea to load the 
volume, too, to make sure everything aligns properly:  Functional with surface 
is the important one, but the anatomical volume is the link between functional 
and surface (i.e., how they get aligned).

> 2. what is the meaning of this error message (attachment 2), which appears
> on selecting the functional volumes?

Again, the funky file naming of two of the volume files (e.g., space, 
parentheses, leading dashes) impedes my ability to check them quickly.  But the 
whole brain anatomical does appear to be a NIfTI volume, rather than just an 
Analyze .hdr file.  I loaded it as a functional volume, and then tried to map 
it to your surface.  I got the same result as trying to map it from disk 
(clicking OK on the stickup you captured).

That warning never got removed after support for nifti .hdr/.img pairs was 
added, but based on my getting the same results using the two paths mentioned 
above, I think you will solve your problem when you solve the misalignment 
between your cropped volume and the whole brain anatomical volume.  
Alternatively, shift the surface to meet the whole brain / functional volume.

Ideally, get the following loaded and aligned in caret:

* whole brain anatomy volume
* functional volume overlay
* surface (probably shifted version of what you have now)

Do this in your subject directory:

find /my/subject/dir -name "*.params" |sort | xargs grep -i min

Capture it to a file if it's a lot.  One of those files has the offset you need.

> thank you.
> 
> 
> Hi John,
>> 
>> Got your upload.  While I couldn't open the cropped volume in caret due to
>> the way it was named, I was able to view the surface contour over the
>> uncropped volume.  See attached capture, which shows an offset.
>> 
>> If you have a SureFit/Caret .params file (not included in the zip), it
>> might contain the [XYZ]min values from the cropping, which might be used
>> to either adjust the functional volume's origin, or more likely apply an
>> affine transform to the surface, to shift it back into alignment with the
>> whole brain volume.  You don't have to blow away your existing coord; just
>> rename the shifted version to indicate the offset.  This can be done via
>> command line or using the Caret: Window: Transformation Matrix editor.
>> The polarity of the shift (+ or -) depends on whether you're shifting the
>> volume or surface, and I always get confused about it.  Usually I try it
>> one way; look at the result like the capture below; and if it looks worse,
>> I try it the other way. ;-)  One of the ways usually does the trick.
>> 
>> Donna
>> 
>> 
>> 
>> On Aug 12, 2015, at 9:14 AM, Donna Dierker 
>> wrote:
>> 
>>> Could you upload your dataset in a zip archive here:
>>> 
>> 
>>> http://pulvinar.wustl.edu/cgi-bin/upload.cgi
>>> 
>>> Specifically I need:
>>> 
>>> * functional volume being mapped
>>> * anatomical volume with which functional volume aligns
>>> * anatomical volume used to generate segmentation -- *cropped*
>>> * fiducial coord file
>>> * topology file
>>> 
>>> I am wondering if the centers of the volumes between the cropped volume
>>> used to generate the surface and the whole brain anatomical volume.
>>> 
>>> 
>>> On Aug 12, 2015, at 1:11 AM, j...@nbrc.ac.in wrote:
>>> 
> 
 
 Ya, sorry for the incomplete query.
 Our interest is to view and threshold fMRI/voxel correlation data over
 the
 fiducial brain surface created out of high res image of individual
 macaques.
 1. we used CARET 5.65 for creating the fiducial surfaces(following the
 caret5 tutorial guide for segmentation).we used individual already
 coregistered high res images for this purpose.
 2. then we tried overlaying the fMRI data(spmT file from analysis using
 spm8) on the fiducial surface (following the procedures from
 http://prefrontal.org/blog/2009/04/using-caret-for-fmri-visualization/
 and the tutorial guides).
 
 we ended up having
 a) fiducial surfaces with fmri data mapped onto it. But the voxel
 coordinates did not match properly with the results in spm8.
 I should tell you one thing that we found: when we overlay whole brain
 fmri results, it matches more or less in x&y axes but not in z axis.
 and
 when we overlay results from explicitly masked analysis(roi), it seems
 to
 be shifted caudally by 2-3mm in R-C axis. same things when checked in
 spm8, shows up to b

Re: [caret-users] doubt regarding fiducial mapping

2015-08-12 Thread Donna Dierker
Could you upload your dataset in a zip archive here:

http://pulvinar.wustl.edu/cgi-bin/upload.cgi

Specifically I need:

* functional volume being mapped
* anatomical volume with which functional volume aligns
* anatomical volume used to generate segmentation -- *cropped*
* fiducial coord file
* topology file

I am wondering if the centers of the volumes between the cropped volume used to 
generate the surface and the whole brain anatomical volume.


On Aug 12, 2015, at 1:11 AM, j...@nbrc.ac.in wrote:

>> 
> 
> Ya, sorry for the incomplete query.
> Our interest is to view and threshold fMRI/voxel correlation data over the
> fiducial brain surface created out of high res image of individual
> macaques.
> 1. we used CARET 5.65 for creating the fiducial surfaces(following the
> caret5 tutorial guide for segmentation).we used individual already
> coregistered high res images for this purpose.
> 2. then we tried overlaying the fMRI data(spmT file from analysis using
> spm8) on the fiducial surface (following the procedures from
> http://prefrontal.org/blog/2009/04/using-caret-for-fmri-visualization/
> and the tutorial guides).
> 
> we ended up having
> a) fiducial surfaces with fmri data mapped onto it. But the voxel
> coordinates did not match properly with the results in spm8.
> I should tell you one thing that we found: when we overlay whole brain
> fmri results, it matches more or less in x&y axes but not in z axis. and
> when we overlay results from explicitly masked analysis(roi), it seems to
> be shifted caudally by 2-3mm in R-C axis. same things when checked in
> spm8, shows up to be well coregistered!
> 
> b)Another issue is we are not able to threshold the caret brain overlays
> in concordance with the thresholds that we use in spm.
> The metric thresholding range (user defined) doesn't seems to represent
> what we really need.
> eg:we tried overlaying FDR corrected voel corrln values, thresh 0.4 on the
> brain in caet and tried a range of metric thresholds(user scale 0-1, put
> display mode-pos,thresh type -user, tried changing user pos thresh values
> to 0.4 and voxels doesn't show up!
> 
> Thank you donna,
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> 
> What software was used to reconstruct the surface?
>> 
>> With freesurfer, there is an offset between the orig.mgz and the surface.
>> And depending on many factors, you might have to flip/rotate the surface
>> to be in the same orientation as the volume (or bring the volume to the
>> surface).
>> 
>> See this thread:
>> 
>> http://www.mail-archive.com/caret-users%40brainvis.wustl.edu/msg02081.html
>> 
>> Also see the "Check Alignment between Normalized Volume and Surface"
>> section here:
>> 
>> http://brainvis.wustl.edu/help/pals_volume_normalization/spm5_normalization_pals.html
>> 
>> Examining the surface contour overlaid on the volum in volume view All is
>> often very enlightening.
>> 
>> 
>> On Aug 11, 2015, at 4:42 AM, j...@nbrc.ac.in wrote:
>> 
 
>>> yes, ours is an individual s surface reconstruction, and so we checked
>>> the
>>> registration in spm8( using  anatomical image used for reconstruction
>>> and
>>> the functional image volumes used for mapping), where the volumes are
>>> coregistered properly, but shows anomaly in caret.
>>> 
>>> thank you
>>> 
>>> 
>>> 
>>> This almost always is because the functional volume is not
 stereotactically registered to the anatomical volume used to generate
 the
 fiducial surface. Is this an atlas surface (e.g., one of the PALS mean
 midthickness surfaces), or is it an individual's surface
 reconstruction?
 If atlas, this could happen if you were trying to map SPM functional
 data
 to the AFNI mid thickness surface, for example, because there are
 noticeable differences between those stereotaxic spaces.
 
 If individual, make sure the functional volume is in register with the
 anatomical volume used to generate the surface.
 
 
 On Aug 10, 2015, at 1:40 AM, j...@nbrc.ac.in wrote:
 
> Hi,
> when i map the functional data onto caret fiducial surface, it
> appears
> that the mapping is shifted in rostrocaudal axis, caudally, by about 2
> -3 mm. anyone has idea what could be possibly wrong here?
> thanks,
> john
> ___
> caret-users mailing list
> caret-users@brainvis.wustl.edu
> http://brainvis.wustl.edu/mailman/listinfo/caret-users
 
 
 ___
 caret-users mailing list
 caret-users@brainvis.wustl.edu
 http://brainvis.wustl.edu/mailman/listinfo/caret-users
 
 
>>> 
>>> ___
>>> caret-users mailing list
>>> caret-users@brainvis.wustl.edu
>>> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>> 
>> 
>> ___
>> caret-users mailing list
>> caret-users@brainvis.wustl.edu
>> h

Re: [caret-users] doubt regarding fiducial mapping

2015-08-12 Thread john
>

Ya, sorry for the incomplete query.
Our interest is to view and threshold fMRI/voxel correlation data over the
fiducial brain surface created out of high res image of individual
macaques.
1. we used CARET 5.65 for creating the fiducial surfaces(following the
caret5 tutorial guide for segmentation).we used individual already
coregistered high res images for this purpose.
2. then we tried overlaying the fMRI data(spmT file from analysis using
spm8) on the fiducial surface (following the procedures from
http://prefrontal.org/blog/2009/04/using-caret-for-fmri-visualization/
and the tutorial guides).

we ended up having
a) fiducial surfaces with fmri data mapped onto it. But the voxel
coordinates did not match properly with the results in spm8.
I should tell you one thing that we found: when we overlay whole brain
fmri results, it matches more or less in x&y axes but not in z axis. and
when we overlay results from explicitly masked analysis(roi), it seems to
be shifted caudally by 2-3mm in R-C axis. same things when checked in
spm8, shows up to be well coregistered!

b)Another issue is we are not able to threshold the caret brain overlays
in concordance with the thresholds that we use in spm.
The metric thresholding range (user defined) doesn't seems to represent
what we really need.
eg:we tried overlaying FDR corrected voel corrln values, thresh 0.4 on the
brain in caet and tried a range of metric thresholds(user scale 0-1, put
display mode-pos,thresh type -user, tried changing user pos thresh values
to 0.4 and voxels doesn't show up!

Thank you donna,





















 What software was used to reconstruct the surface?
>
> With freesurfer, there is an offset between the orig.mgz and the surface.
> And depending on many factors, you might have to flip/rotate the surface
> to be in the same orientation as the volume (or bring the volume to the
> surface).
>
> See this thread:
>
> http://www.mail-archive.com/caret-users%40brainvis.wustl.edu/msg02081.html
>
> Also see the "Check Alignment between Normalized Volume and Surface"
> section here:
>
> http://brainvis.wustl.edu/help/pals_volume_normalization/spm5_normalization_pals.html
>
> Examining the surface contour overlaid on the volum in volume view All is
> often very enlightening.
>
>
> On Aug 11, 2015, at 4:42 AM, j...@nbrc.ac.in wrote:
>
>>>
>> yes, ours is an individual s surface reconstruction, and so we checked
>> the
>> registration in spm8( using  anatomical image used for reconstruction
>> and
>> the functional image volumes used for mapping), where the volumes are
>> coregistered properly, but shows anomaly in caret.
>>
>> thank you
>>
>>
>>
>> This almost always is because the functional volume is not
>>> stereotactically registered to the anatomical volume used to generate
>>> the
>>> fiducial surface. Is this an atlas surface (e.g., one of the PALS mean
>>> midthickness surfaces), or is it an individual's surface
>>> reconstruction?
>>> If atlas, this could happen if you were trying to map SPM functional
>>> data
>>> to the AFNI mid thickness surface, for example, because there are
>>> noticeable differences between those stereotaxic spaces.
>>>
>>> If individual, make sure the functional volume is in register with the
>>> anatomical volume used to generate the surface.
>>>
>>>
>>> On Aug 10, 2015, at 1:40 AM, j...@nbrc.ac.in wrote:
>>>
 Hi,
  when i map the functional data onto caret fiducial surface, it
 appears
 that the mapping is shifted in rostrocaudal axis, caudally, by about 2
 -3 mm. anyone has idea what could be possibly wrong here?
 thanks,
 john
 ___
 caret-users mailing list
 caret-users@brainvis.wustl.edu
 http://brainvis.wustl.edu/mailman/listinfo/caret-users
>>>
>>>
>>> ___
>>> caret-users mailing list
>>> caret-users@brainvis.wustl.edu
>>> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>>>
>>>
>>
>> ___
>> caret-users mailing list
>> caret-users@brainvis.wustl.edu
>> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>
>
> ___
> caret-users mailing list
> caret-users@brainvis.wustl.edu
> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>
>

___
caret-users mailing list
caret-users@brainvis.wustl.edu
http://brainvis.wustl.edu/mailman/listinfo/caret-users


Re: [caret-users] doubt regarding fiducial mapping

2015-08-11 Thread Donna Dierker
What software was used to reconstruct the surface?

With freesurfer, there is an offset between the orig.mgz and the surface.  And 
depending on many factors, you might have to flip/rotate the surface to be in 
the same orientation as the volume (or bring the volume to the surface).

See this thread:

http://www.mail-archive.com/caret-users%40brainvis.wustl.edu/msg02081.html

Also see the "Check Alignment between Normalized Volume and Surface" section 
here:

http://brainvis.wustl.edu/help/pals_volume_normalization/spm5_normalization_pals.html

Examining the surface contour overlaid on the volum in volume view All is often 
very enlightening.


On Aug 11, 2015, at 4:42 AM, j...@nbrc.ac.in wrote:

>> 
> yes, ours is an individual s surface reconstruction, and so we checked the
> registration in spm8( using  anatomical image used for reconstruction and
> the functional image volumes used for mapping), where the volumes are
> coregistered properly, but shows anomaly in caret.
> 
> thank you
> 
> 
> 
> This almost always is because the functional volume is not
>> stereotactically registered to the anatomical volume used to generate the
>> fiducial surface. Is this an atlas surface (e.g., one of the PALS mean
>> midthickness surfaces), or is it an individual's surface reconstruction?
>> If atlas, this could happen if you were trying to map SPM functional data
>> to the AFNI mid thickness surface, for example, because there are
>> noticeable differences between those stereotaxic spaces.
>> 
>> If individual, make sure the functional volume is in register with the
>> anatomical volume used to generate the surface.
>> 
>> 
>> On Aug 10, 2015, at 1:40 AM, j...@nbrc.ac.in wrote:
>> 
>>> Hi,
>>>  when i map the functional data onto caret fiducial surface, it appears
>>> that the mapping is shifted in rostrocaudal axis, caudally, by about 2
>>> -3 mm. anyone has idea what could be possibly wrong here?
>>> thanks,
>>> john
>>> ___
>>> caret-users mailing list
>>> caret-users@brainvis.wustl.edu
>>> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>> 
>> 
>> ___
>> caret-users mailing list
>> caret-users@brainvis.wustl.edu
>> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>> 
>> 
> 
> ___
> caret-users mailing list
> caret-users@brainvis.wustl.edu
> http://brainvis.wustl.edu/mailman/listinfo/caret-users


___
caret-users mailing list
caret-users@brainvis.wustl.edu
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Re: [caret-users] doubt regarding fiducial mapping

2015-08-11 Thread john
>
yes, ours is an individual s surface reconstruction, and so we checked the
registration in spm8( using  anatomical image used for reconstruction and
the functional image volumes used for mapping), where the volumes are
coregistered properly, but shows anomaly in caret.

thank you



This almost always is because the functional volume is not
> stereotactically registered to the anatomical volume used to generate the
> fiducial surface. Is this an atlas surface (e.g., one of the PALS mean
> midthickness surfaces), or is it an individual's surface reconstruction?
> If atlas, this could happen if you were trying to map SPM functional data
> to the AFNI mid thickness surface, for example, because there are
> noticeable differences between those stereotaxic spaces.
>
> If individual, make sure the functional volume is in register with the
> anatomical volume used to generate the surface.
>
>
> On Aug 10, 2015, at 1:40 AM, j...@nbrc.ac.in wrote:
>
>> Hi,
>>   when i map the functional data onto caret fiducial surface, it appears
>> that the mapping is shifted in rostrocaudal axis, caudally, by about 2
>> -3 mm. anyone has idea what could be possibly wrong here?
>> thanks,
>> john
>> ___
>> caret-users mailing list
>> caret-users@brainvis.wustl.edu
>> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>
>
> ___
> caret-users mailing list
> caret-users@brainvis.wustl.edu
> http://brainvis.wustl.edu/mailman/listinfo/caret-users
>
>

___
caret-users mailing list
caret-users@brainvis.wustl.edu
http://brainvis.wustl.edu/mailman/listinfo/caret-users


Re: [caret-users] doubt regarding fiducial mapping

2015-08-10 Thread Donna Dierker
This almost always is because the functional volume is not stereotactically 
registered to the anatomical volume used to generate the fiducial surface. Is 
this an atlas surface (e.g., one of the PALS mean midthickness surfaces), or is 
it an individual's surface reconstruction?  If atlas, this could happen if you 
were trying to map SPM functional data to the AFNI midthickness surface, for 
example, because there are noticeable differences between those stereotaxic 
spaces.

If individual, make sure the functional volume is in register with the 
anatomical volume used to generate the surface.


On Aug 10, 2015, at 1:40 AM, j...@nbrc.ac.in wrote:

> Hi,
>   when i map the functional data onto caret fiducial surface, it appears
> that the mapping is shifted in rostrocaudal axis, caudally, by about 2
> -3 mm. anyone has idea what could be possibly wrong here?
> thanks,
> john
> ___
> caret-users mailing list
> caret-users@brainvis.wustl.edu
> http://brainvis.wustl.edu/mailman/listinfo/caret-users


___
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[caret-users] doubt regarding fiducial mapping

2015-08-10 Thread john
Hi,
   when i map the functional data onto caret fiducial surface, it appears
that the mapping is shifted in rostrocaudal axis, caudally, by about 2
-3 mm. anyone has idea what could be possibly wrong here?
thanks,
john
___
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caret-users@brainvis.wustl.edu
http://brainvis.wustl.edu/mailman/listinfo/caret-users