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Hi Freesurfer Experts,
Is there anything that could be done to improve the surface definitions for
this particular subject (attached)? The pial and white matter boundaries in
the cortex are generally accurate though.
Thank you.
Best Wishes,Shane_
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Hi Freesurfer Experts,
I am trying to obtain coregister diffusion data b0 with T1.
One problem is that I do not have any means to correct for EPI distortions.
Because of this, I am experimenting with DOF = 9 and DOF = 12. The mincost for
12 was consi
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Hi Freesurfer Tema,
I am trying to use vol2subfield to extract DTI measurements like FA and MD.
For this purpose, should I be using the
rh.hippoAmygLabels-T1.v21.CA.FSvoxelSpace.mgz or
rh.hippoAmygLabels-T1.v21.CA.mgz ?
Thank you!_
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Hi PETSURFERs,
A quick question to the group: Does any one have experience using PETSURFER on
dynamic AV1451 scans? How can I know whether the MRTM1 or MRTM2 using midbrains
(due to off target AV1451 binding) is suitable for my data?
Thank you!
Best
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Hi Freesurfer Team,
I have used mri_segstats to get ythe mean PET uptake across all the
parcellations in the WMPARC space. These values were calculated in the native
PET space (following the DTI tutorial). A reviewer asked what is the grey
matter pro
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Thanks, Doug. I think the command is MCFLIRT.
https://fsl.fmrib.ox.ac.uk/fsl/fslwiki/MCFLIRT
Best Wishes,Shane
On Friday, May 3, 2019, 6:18:54 PM GMT+1, Shane Schofield
wrote:
Hi Freesurfer Team,
How may I align 5 volumes of my PET data
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Hi Freesurfer Team,
How may I align 5 volumes of my PET data ( 5 min acquisitions each) to a mean
image for motion correction across the acquisition? I can use mri_concat to get
the the mean image, but I am not sure how to do the realignment after tha
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Hi Doug, thanks for the explanation. My question is more related to how we
might go about knowing what are the high binding regions for any tracer? If I
am going to do an FDG-PET study, will the HB region parameters be different
from a [11C]-PK11195
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Hello PetSurfer Developers
On the tutorial page, I do not understand this part:
--km-hb 11 12 13 50 51 52 specifies the ROIs to use as the high-binding region
if using MRTM2. This creates km.hb.tac.nii.gz with the value for the
high-binding region for
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Hi Freesurfer
A reviewer asked whether there are concerns about whether Freesurfer may obtain
accurate cortical thickness data in people with developmental conditions - the
main focus in my study. I did a search and could not find any validation
stud
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Hi Doug, it is kinetic modelling, not uptake. Thank you.
On Monday, August 13, 2018, 10:36:13 AM GMT+1, Shane Schofield
wrote:
Hello Petsurfers!
A few of my subjects ended up with vertices that had outlier PET values after I
followed the
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Hello Petsurfers!
A few of my subjects ended up with vertices that had outlier PET values after I
followed the PetSurfer steps. Most of the binding potentials are in the range
of 0 - 3. Looking at the histogram though there are a couple of vertices wi
Hi Freesurfer Team,
I try to calculate a within-subject decrease in cortical thickness over 2
years, but the MRI scanner was changed during the project. Is it still possible
to do that using the longitudinal stream in Freesurfer?
Thanks.
Best Wishes,Shane_
Hi Freesurfer,
I have two question about the different partial volume correction options.
Basically how is the --mg method different from the --mgx? I cannot seem to
find papers that have compared these methods. Any opinions on this?
Does this have any effect on the region of interest GTM result
st 16, 2017, 10:46:09 PM GMT+1, Douglas N Greve
wrote:
SUVR you can. BP is a little trickier because BP estimation is a
nonlinear operation that can be biased by noise. Probably it comes out
similarly.
On 08/16/2017 02:50 PM, Shane Schofield wrote:
> Hi Dr Greve,
>
> On a similar note,
Hi Dr Greve,
On a similar note, can I use the Petsurfer on PET data that have already been
averaged into a single frame 3D volume instead of 4D? Example, SUVR and BPND
data.
Thanks for your help again.
On Tuesday, August 15, 2017, 9:09:33 AM GMT+1, Shane Schofield
wrote:
Hello Dr Greve,
I
subject (takes an hour or so), then add
--seg gtmseg.mgz to the cmd line
On 08/14/2017 04:12 PM, Shane Schofield wrote:
> Hi Dr Greve,
>
> Are the settings correct to do partial volume correction of my MD images?
>
> mri_gtmpvc --i subject/dtrecon/adc.nii.gz --reg
> subject/dt
; >
>> >not really - it totally depends on the size of the effect you are
>> looking
>> >for. I would be *very* careful about partial volume effects though
>> >
>> >cheers
>> >Bruce
>> >On Fri,
>> >11 Aug 2017, Shane Schof
t the very least you should probably regress
> thickness out.
>
> cheers
> Bruce
>
> On Sat, 12 Aug 2017, Shane Schofield wrote:
>
>> Thank you both.
>>
>> How can I deal with partial volume in this case? Would it be possible
>> to use
>> the parti
>Hi Shane
>
>not really - it totally depends on the size of the effect you are looking
>for. I would be *very* careful about partial volume effects though
>
>cheers
>Bruce
>On Fri,
>11 Aug 2017, Shane Schofield wrote:
>
>> Appreciate it Dr Bruce. Do you have gui
e surface-based
registration I believe. Use mri_vol2surf to sample the FA onto the surface.
After that it is identical to a thickness study
cheers
Bruce
On Fri, 11 Aug 2017, Shane Schofield
wrote:
> Thanks Dr Yendiki.
>
> I am more interested to compare MD in grey matter regions
:
#yiv9314780658 P {margin-top:0;margin-bottom:0;}What effect are you trying to
measure with MD on the cortex?
From: Shane Schofield [shane.schofi...@yahoo.com]
Sent: Friday, August 11, 2017 3:12 AM
To: Freesurfer Support List; Yendiki, Anastasia
Subject: Re: Mean diffusivity on cortex?
Thanks
tutorial.
On Friday, August 11, 2017, 7:03:49 AM GMT+1, Shane Schofield
wrote:
Hi DTI Experts,
Is it sensible to do comparisons of MD on the cortex surface like a normal
cortical thickness comparisons between group? If the answer is yes, are there
recommended on smoothing ?
DT_RECON has been
Hi DTI Experts,
Is it sensible to do comparisons of MD on the cortex surface like a normal
cortical thickness comparisons between group? If the answer is yes, are there
recommended on smoothing ?
DT_RECON has been completed in Freesurfer.
Thank you.
__
Hi Freesurfer Experts,
Does anyone know how to deal with situations where the part of the brain is not
being captured in aseg.mgz or in the surfaces? I have attached some
screenshots. I have tried adding control points but it is not working. Thanks
for helping.
Best,Shane
___
esday, May 9, 2017 5:58 PM, Douglas N Greve
wrote:
When the pixel data are flipped, you are actually changing the way that
the data are stored on disk (while keeping the direction info in the
header constant).
On 05/09/2017 12:52 PM, Shane Schofield wrote:
> Dear Doug,
> I am try
Dear Doug,I am trying to flip some PET images so that they are in the same
orientation as the T1.I came across this post
http://www.mail-archive.com/freesurfer@nmr.mgh.harvard.edu/msg29281.htmlCan you
explain what what it means to change the pixel data? Should I use pix or
without pix? For cont
these are the ids for left and right cblum wm and gm
On 04/28/2017 06:13 AM, Shane Schofield wrote:
> Hello PetSurfer and Freesurfer Developers,
>
> I am using PetSurfer to obtain PVC SUVR images . I have already used
> mri_concat to derive the mean images over three acquisitions (templ
Hello PetSurfer and Freesurfer Developers,
I am using PetSurfer to obtain PVC SUVR images . I have already used mri_concat
to derive the mean images over three acquisitions (template image).
After gtmseg amd mri_coreg, I want to get the SUVR map with whole cerebellum as
the reference (instead o
, that is correct. An alternative would be editing the aseg directly.
Editing the wm will help the surfaces but not correct the aseg.
But as Antonin suggests, try running with -bigventricles and see if that
fixes your problems
cheers
Bruce
On Sun, 23 Apr 2017, Shane Schofield wrote:
> Th
Dear Doug,
If I want to create a new volume that is registered to the MNIspace (using
mni1525reg), can I mask out other voxels that are not part of the mni template
brain? It is a PET volume (already in individual space using bbregister) that
has noisy signals in non-brain regions.
Thank you.
Hi Freesurfer Team,
I am running recon-all on Freesurfer version 6. A few of my subjects have “XL
defect detected …” and their recon-all have been running for more than 20
hours. I hope this is not a silly question, but will this XL defect be
corrected eventually…?
Another question, what are
Hello,
Thanks. Seems very interesting!
Is there any way to run this on Mac?
Cheers
--
Shane Schofield ___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
The information in
Hi Freesurfer,
How can I get the LGI measurements for each brain region in Desikan atlas?
Instead of getting thickness with aparcstats2table, I want the gyrification
instead.
Thank you.
Cheers,
Shane
--
Shane Schofield___
Freesurfer mailing list
Fr
Hi,
I have 3 beginner questions about the use of mri_glmfit-sim
1. Under what type of circumstances should I run mri_glmfit-sim with
permutation simulations?
2. The voxel threshold of 0.01 (cache 2) is used a lot. Is this too lenient in
cortical thickness comparisons?
3. About the sign of the
Hi Z K,
Thanks. I had thought that the recon-all speed will run much slower on the
external HD but 10 hours seems to be the average recon-all time so I am
pleasantly surprised.
Best Wishes,
Shane
___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard
Hello,
I am new to image analysis and I have a basic question: is it recommended to
run recon-all on external hard-disks (USB3.0) to save space on my laptop? Will
there be any issues with regards to the performance of recon-all? I have just
finished a recon-all on 1 subject and it took me 10 ho
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