That just means that the scan did not complete for some reason. You can use
them so long as your code does not assume all subjects have 1200 time points.
Peace,
Matt.
From:
>
on behalf of Ruby Kong
the
matrix.
I don't think we have decided what the "best possible manner" is for dealing
with the distance bias (or we would already have dealt with it).
Regards,
Karthik
On Oct 6, 2017, at 7:32 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
We did it fo
I believe both binaries will use the grad_dev to perform the correct described
in the bvals and bvecs in a voxelwise manner.
Peace,
Matt.
From:
>
on behalf of Athanasia Metoki
rfMRI_REST_Concat
${FSL_FIXDIR}/training_files/HCP_hp2000.RData
I also tried to input the data as a list file, but the script didn’t work with
error. It seems to get only one 4D rfMRI data set as input.
That’s why I concatenated each run of rfMRI data set.
Could you please confirm whether the above p
error. It seems to get only one 4D rfMRI data set as input.
That’s why I concatenated each run of rfMRI data set.
Could you please confirm whether the above procedures are correct or not?
Thanks again.
Sang-Young
On Oct 6, 2017, at 3:57 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:gla
e
to me.
Do you have any suggestions on how I could best compute this proxy?
Regards,
Karthik
On Oct 5, 2017, at 8:50 AM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
Indeed I think we would need to know what you needed the distance for to know
how best
rd one)?
The third one should be processed with group ICA, right?
What about the second one? This is processed with method 3 on above list?
Thanks.
Sang-Young
On Oct 6, 2017, at 5:40 AM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
There is a beta version
the distance bias in tractography, so I want to use some proxy
for actual connection distance between ROI pairs. Using tractography itself to
account for its own bias against long-distance connections doesn’t make sense
to me.
Do you have any suggestions on how I could best compute this prox
rtices?
If you can only get the distances in white matter voxels, or only the distances
from the seed point, things could get challenging if you want to use different
seeding strategies.
Tim
On Fri, Oct 6, 2017 at 6:24 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>&g
..@mst.edu<mailto:tsc...@mst.edu>> wrote:
Right, I wasn't very precise in my wording. I was thinking of the
"tractography distance bias" as the amount of the bias that is above and beyond
the real biological distance relationship.
Tim
On Fri, Oct 6, 2017 at 4:36
There is a beta version of a multi-run ICA+FIX pipeline available in the HCP
Pipeline’s repository. For 5 minute runs, I would expect combining across runs
to be best. We haven’t tested combining across sessions yet, so you would have
to check that that was working okay if you wanted to try
Users FAQ. Would this be also your preference. Is there a reference or
mathematical definitions for these functions (other than the obvious ones), so
I can do a mathematical comparison between the two approaches?
Heracles Panagiotides, PhD
From: Harms, Michael
Sent: Thursday, October 05, 2017 1
MRI data files
Does anyone know how the concatenation (see discussion below) of the ROI
extracted time series needs to happen? Do I simply concatenate the time series
as a temporal sequence, rfMRI_REST2_LR followed by rfMRI_REST2_RL ?
Thanks again for the kind help.
Heracles Panagiotides, PhD
went into such detail..
Best wishes,
Romuald
--
Message: 2
Date: Tue, 3 Oct 2017 00:11:35 +
From: "Glasser, Matthew" <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Subject: Re: [HCP-Users] rfMRI data files
To: hercp <he...@uw.edu&
Indeed I think we would need to know what you needed the distance for to know
how best to compute it. For things like MR artifacts, a 3D distance might be
most appropriate. For something like smoothing, a geodesic distance would be
appropriate. For something neurobiological, the tractography
Right we will recommend using the areal classifier to find these areas rather
than the group parcellation once the areal classifier is available.
Peace,
Matt.
From:
>
on behalf of Timothy Coalson
Yes you ideally would analyze all of the resting state fMRI runs per subject.
They have different phase encoding directions, so you should always analyze an
equal amount of each. Be sure to demean and perhaps variance normalize prior
to concatenating.
Peace.
Matt.
From:
Add the files to a spec file and then open the spec file. Or perhaps it would
be helpful to use quotes around your arguments.
Peace,
Matt.
From:
>
on behalf of Keren Kotler
Dear HCP Users,
A frequently discussed topic on the HCP-Users mailing list is how to clean HCP
fMRI data above and beyond the recommended spatial ICA + FIX cleanup that has
already been carried out. Several papers have noted that there is residual
structured noise in HCP data and have
In general one wants to get as many gradient directions as possible.
Perhaps Mike knows the answer to your other question.
Matt.
On 9/28/17, 2:59 AM, "hcp-users-boun...@humanconnectome.org on behalf of
Jeffrey Spielberg"
I¹d hope not more than another month or two.
Peace,
Matt.
On 9/21/17, 1:11 PM, "hcp-users-boun...@humanconnectome.org on behalf of
Nina de Lacy" wrote:
>Hi there:
>
>I just wanted to check in and see if there was any
Brain areas are not spheres. I don’t think this is a good approach. What is
it that you are trying to do?
Peace,
Matt.
From:
>
on behalf of Athanasia Metoki
This is built into the CIFTI format for the future, however we do not yet have
an algorithm for making individual subject cerebellar surfaces. I believe a
“Colin” individual surface is available somewhere and perhaps David knows the
details.
Peace,
Matt.
From:
does it works to keep both cortical and
subcortical gray matter?
Thank you again,
Carole
Le 18 sept. 2017 à 17:08, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> a écrit :
This should be possible with wb_command -cifti-cross-correlation. You would
create a C
Myelin maps are only for the cortex so you can omit the -volume-all
data_sub.nii portion of the command.
Peace,
Matt.
From:
>
on behalf of Sang-Young Kim >
Date:
This should be possible with wb_command -cifti-cross-correlation. You would
create a CIFTI dense timeseries file of the subcortical region of interest and
a CIFTI parcellated timeseries using the parcellation of your choice. You
could then visualize the results in wb_view (depending on the
I would ask on the FreeSurfer mailing list how to convert those file types to
GIFTI as we are not familiar with them.
Peace,
Matt.
From:
>
on behalf of Timothy Coalson >
addpath('${FSL_MATLAB_PATH}'); addpath('${FSL_FIX_CIFTIRW}');"
to
ML_PATHS="restoredefaultpath; addpath('${FSL_MATLAB_PATH}');
addpath('${FSL_FIX_CIFTIRW}');"
-Keith
On Mon, Sep 11, 2017 at 5:54 PM, Sang-Young Kim
<sykim...@gmail.com<mailto:sykim...@gmail.com>> wrote:
Yes, I’m
Are you using CIFTI data? Is this the compiled version of matlab or the
interpreted version?
Peace,
Matt.
On 9/11/17, 4:19 PM, "hcp-users-boun...@humanconnectome.org on behalf of
Sang-Young Kim" wrote:
>Dear HCP experts:
e then, since the linear detrend has been
already applied, right?
Heracles Panagiotides, PhD
From: Glasser, Matthew
Sent: Friday, September 08, 2017 9:48 AM
To: hercp ; HUMAN CONNECTOME
Subject: Re: [HCP-Users] rfMRI processing
We just use a linear detrend.
Matt.
From: hercp <he...@uw.edu
are always very helpful.
Would you recommend not using any temporal filter at all?
Heracles Panagiotides, PhD
From: Glasser, Matthew
Sent: Thursday, September 07, 2017 7:53 PM
To: NEUROSCIENCE tim ; hercp
Cc: HUMAN CONNECTOME
Subject: Re: [HCP-Users] rfMRI processing
Also, I
Also, I wouldn’t recommend doing that. There is plenty of BOLD signal outside
those frequencies.
Peace,
Matt.
From:
>
on behalf of Timothy Coalson >
Date: Thursday,
Right. Basically we are suspicious of defining areas based on statistical
thresholds, as these are unlikely to reflect biological boundaries in the
brain, but rather the vagaries of the statistical thresholding approach and the
noise distribution.
Peace,
Matt.
From:
The TR=0.72s, but I think that is correct.
Peace,
Matt.
From:
>
on behalf of "HINDRIKS, RIKKERT"
>
Date: Tuesday, September 5, 2017 at 8:48 AM
To:
have an "across parcels"
option, that would be what "-volume-smoothing" is for. This option exists in
cifti commands because cifti already contains the parcel ROIs, and we decided
the default would be to treat them separately.
Tim
On Fri, Sep 1, 2017 at 2:11 PM, Glasser, M
Please use the latest version of the HCP pipelines and the latest version of
FSL. Hopefully this user guide can be amended to suggest this, as it is from 2
years ago.
Peace,
Matt.
From:
>
on behalf of
LR.surf.gii
for a right-hemisphere ROI.
Now these .gii files are the ones I provide to probtrackx.
Regards,
Karthik
From: Glasser, Matthew <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Sent: Friday, September 1, 2017 4:30:31 PM
To: Gopalakrishnan, Ka
The white matter surfaces used were:
100206.L.white_MSMAll.32k_fs_LR.surf.gii
100206.R.white_MSMAll.32k_fs_LR.surf.gii
Thanks!
Karthik
From: Glasser, Matthew <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Sent: Friday, September 1, 2017 4:14:03 PM
To
e-masks.txt and the file targets.txt contain newline-separated
paths to each of the 360 ROIs (.gii files).
Thanks!
Karthik
From: Glasser, Matthew <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Sent: Friday, September 1, 2017 4:06:15 PM
To
-targetmasks=targets.txt --os2t --s2tastext
Thanks!
Karthik
From: Glasser, Matthew <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Sent: Friday, September 1, 2017 8:16:51 AM
To: Gopalakrishnan, Karthik;
HCP-Users@humanconnectome.org<mailto:HCP-Users@humanconnectome.org>
Sub
dy contains the parcel ROIs, and we decided
the default would be to treat them separately.
Tim
On Fri, Sep 1, 2017 at 2:11 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
I guess I don’t know why one would want to smooth across the known boundaries,
but th
University School of Medicine
Department of Psychiatry, Box 8134
660 South Euclid Ave.Tel: 314-747-6173
St. Louis, MO 63110 Email:
mha...@wustl.edu<mailto:mha...@wustl.edu>
From:
<hcp-users-boun...@humanconnectome.org<mailto:hcp-use
1. That command for the surface is not quite what you are looking for. For
the surface, the left and right hemisphere vertices are already in register
(meaning that vertices with the same number will be in the anatomically
corresponding location). You would need to translate between the
Can you post your probtrackx call?
Peace,
Matt.
From:
>
on behalf of "Gopalakrishnan, Karthik"
>
Date: Thursday, August 31, 2017 at 9:27 PM
To:
What kind of resolution are we talking about? The resolution parameters
control the greyordinates space and the final volume space.
Peace,
Matt.
From:
>
on behalf of Timothy Coalson
ch provides a new way
to me when I have FSL running problems in the future.
Best regards,
Xinyang
At 2017-08-29 10:29:57, "Glasser, Matthew"
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
If this is with FSL’s GUI, you might need to ask about it on the FSL list.
Pea
If this is with FSL’s GUI, you might need to ask about it on the FSL list.
Peace,
Matt.
From:
>
on behalf of Xinyang Liu >
Date: Monday, August 28, 2017 at
but I'd like to display the Yeo's atlas in its original
form for the figure.
As far as that registration goes, how would I go about doing so?
On Fri, Aug 25, 2017 at 10:17 AM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
You might actually have to rema
You might actually have to remap that to the subject’s volume using the
individual surfaces and then back to the merged surface. The reason is that by
merging the surfaces you change the topology, and in such a way that we cannot
use surface registration to handle things. Tim may have
Subject: Re: [HCP-Users] Tractography
Thanks, Matt. Which files are the output of the Bedpostx process? I am
currently looking at subject 116524. These are files I was able to download.
[2017-08-24_9-36-36]
Once again, thank you for your help.
Heracles Panagiotides, PhD
From: Glasser
Also as Steve has reminded me, you can download the Bedpostx outputs
pre-computed.
Peace,
Matt.
From:
>
on behalf of Matt Glasser >
Date: Thursday, August 24,
That is the price one pays for really high spatial and angular resolution
diffusion data. You can accelerate things quite a bit on CUDA capable GPUs.
Peace,
Matt.
From:
>
on behalf of hercp
While that is true, what I suggested is the equivalent at least as far as
measuring the smoothness of the unstructured noise goes.
Matt.
From:
>
on behalf of "Harms, Michael"
You could regress out the signal ICA components from the sICA+FIX cleaned
volume timeseries and use the resulting residuals for this.
Peace,
Matt.
From:
>
on behalf of Francesco
otiropou...@ndcn.ox.ac.uk>>
wrote:
Hi
you need to install CUDA 7.5 and have
LD_LIBRARY_PATH=$LD_LIBRARY_PATH:/usr/local/cuda/lib64
export LD_LIBRARY_PATH
in your ~/.bashrc, assuming that /usr/local/cuda is where you have installed
CUDA, otherwise replace accordingly.
Cheers
Stam
On 22
ocal/cuda is where you have installed
CUDA, otherwise replace accordingly.
Cheers
Stam
On 22 Aug 2017, at 20:01, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
Actually that looks like a cuda library error and your pipeline setup looks
fine. You might
="${RawDataDir}/${SubjectID}_3T_DWI_dir113_PA.nii.gz"
EchoSpacing=0.77
PEdir=2
Gdcoeffs="${HCPPIPEDIR_Config}/coeff_AS82_Prisma.grad"
*****
Thanks.
Sang-Young
On Aug 22, 2017, at 2:44 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
I mean the la
bal/scripts
export HCPPIPEDIR_tfMRIAnalysis=${HCPPIPEDIR}/TaskfMRIAnalysis/scripts
**********
Thanks.
Sang-Young
On Aug 22, 2017, at 2:38 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
Need to know the variables in the laugh
ingBatch.sh
>
>I believe all environment variables are correctly set in
>"SetUpHCPPipeline.sh".
>
>Thanks.
>
>Sang-Young
>
>> On Aug 22, 2017, at 2:28 PM, Glasser, Matthew <glass...@wustl.edu>
>>wrote:
>>
>> How did you call the pipeline?
&g
How did you call the pipeline?
Peace,
Matt.
On 8/22/17, 10:57 AM, "hcp-users-boun...@humanconnectome.org on behalf of
Kim, Sang-Young" wrote:
>Dear HCP experts:
>
>We have diffusion MRI data acquired from Siemens Prisma 3 T
I suppose it would be reasonable to make unsmoothed individual subject volume
data available, however that isn’t going to be high on the priority list given
available resources. In my opinion the smoothed volume data shouldn’t have
been made available in the first place, because they were
All of the registration and distortion correction has already been done. All
of the T1w images should be in the same mm space, but you may wish to use the
file with 1.25 in the name for 3T diffusion and 1.05 in the name for 7T
diffusion if you want to use a tool like FSLView that requires the
wb_command -cifti-gradient and wb_command -cifti-correlation-gradient. There
are also -metric-gradient for GIFTI files and -volume-gradient for NIFTI files.
Peace,
Matt.
From:
>
on behalf of Sang-Yun Oh
For the 32k 2mm average spacing surfaces you can find the standard medial
wall definitions here:
https://github.com/Washington-University/Pipelines/blob/master/global/templ
ates/91282_Greyordinates/L.atlasroi.32k_fs_LR.shape.gii
Nope, you can do the tractography directly from the surfaces using FSL:
https://fsl.fmrib.ox.ac.uk/fsl/fslwiki/FDT/UserGuide#Using_surfaces Use the
surfaces in ${StudyFolder}/${Subject}/T1w/fsaverage_LR32k. White surfaces are
good for counting and pial surfaces are good for stopping. There
Hi Sean,
We can discuss off list.
Peace,
Matt.
On 8/14/17, 3:23 AM, "hcp-users-boun...@humanconnectome.org on behalf of
Sean Tobyne" wrote:
>Hello,
>
>Is it known when the option for user submissions to BALSA will be
It looks like you have the correct understanding of this. One cannot easily
apply the gradient nonlinearity effects on the diffusion gradients to the
images, as really you need to apply them to the bvals and bvecs.
Peace,
Matt.
From:
Subject: Re: [HCP-Users] The best set of annotations for any MRI scan?
Hi Matt,
Thanks for your response, I mean a set of human added labels that are
associated with specific locations of the scan.
Best,
anita
On Thu, Aug 10, 2017 at 9:52 AM, Glasser, Matthew
<glass...@wustl.edu<mailto
Indeed the conversion from FreeSurfer annot format to GIFTI label format using
FreeSurfer’s mris_convert does not preserve the probabilities (instead coloring
every vertex with non-zero probability as a label). Really though, FreeSurfer
only provides those labels on individual subjects as a
It should work if you skip the last step and use the dlabel file.
Peace,
Matt.
From: Xavier Guell Paradis >
Date: Wednesday, August 9, 2017 at 9:43 AM
To: Timothy Coalson >, Matt Glasser
wb_command -cifti-create-dense-scalar and then wb_command -cifti-label-import
with an appropriate label tabel. Alternatively, wb_command
-volume-label-import and wb_command -cifti-create-label.
Peace,
Matt.
From:
There is not enough information in this question to answer. I would need to
know what files you are talking about and what you are trying to do.
Peace,
Matt.
From:
>
on behalf of 罗
of Mental Disorders
Washington University School of Medicine
Department of Psychiatry, Box 8134
660 South Euclid Ave.Tel:
314-747-6173<tel:(314)%20747-6173>
St. Louis, MO 63110 Email:
mha...@wustl.edu<mailto:mha...@wustl.edu>
1. Yes
2. We use dcm2nii.
3. Probably
I would use offline so you are sure that all of your images are being corrected
the same way and have control over how the resampling is being done (i.e. not
adding blurring from trilinear interpolation).
Peace,
Matt.
From:
That means they didn¹t complete all of the scans. It is up to you whether
you want to include such subjects in your study.
Peace,
Matt.
On 8/3/17, 10:00 PM, "hcp-users-boun...@humanconnectome.org on behalf of
Fang-Cheng Yeh"
ubject space using the MSMAll surfaces in the subject directory of the T1w
folders. My result is data associated with those surfaces and I was planning on
averaging the data across participants.
Claude
On 04.08.2017 00:28, Glasser, Matthew wrote:
Tractography has quite strong folding-related bia
They were run in the CIFTI greyordinates space. As it turns out, ICA results
from well aligned data look different from those of poorly aligned data, as one
gets many components representing misalignment if the data are not well aligned.
Peace,
Matt.
From: James Morrow
This is challenging for several reasons: Standard volumetric data don’t have
good alignment of cortical areas, and cortical areas are complex patches on a
convoluted surface not 3D points, so MNI coordinates are not especially
meaningful as a way of determining if results are the same across
es
University of Reading
____________
From: Glasser, Matthew <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Sent: 28 July 2017 13:02:39
To: Nicolo Biagi;
hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>; Brown, Tim
Subject: Re: [HCP-Users] Problems with the HCP Pipel
1. TI=1000 actually separates the CSF/Grey/White peaks of the the histogram
more evenly than TI=900ms (CSF and Grey too close) or TI=1100 (Grey and White
too close). I don’t understand why the FreeSurfer group has recommended
TI=1100 as it wouldn’t seem to make things easier for their
t trickier.
Do you have an example FSL command for a HCP subject? I can’t really figure out
what I need to do, and what HCP has already done. For example, do any
transforms need to be calculated? Do I just need the subject surface to
fsaverage transform?
Thanks again,
Max
On Aug 1, 2017, at 2
You can use wb_command -cifti-separate to get GIFTI label files out and then
use https://fsl.fmrib.ox.ac.uk/fsl/fslwiki/FDT/UserGuide#Using_surfaces
Peace,
Matt.
From:
>
on behalf of Max Bertolero
below), but not in Python. I
>can read cifti image in python.
>
>f=image.load_img(filename)
>
>But how do I get coordinates of the subcortical structures. I code
>snippet would be appreciated.
>
>Thank you,
>Best,
>Anand
>
>___
For the volume structures these are in the CIFTI header, however for the
surfaces there are no veridical xyz coordinates, it all depends on the
surface model you are using. In general we recommend only using 3D
coordinates of individual subject¹s midthickness surfaces (or in special
circumstances
They aren¹t yet available however we hope to get them out soon when there
is bandwidth available for the appropriate people.
Peace,
Matt.
On 7/27/17, 2:39 PM, "hcp-users-boun...@humanconnectome.org on behalf of
K. Wagstyl"
1. Yes
2. Yes
3. Use the preprocessed data which has all files preprocessed and combined
appropriately in ${StudyFolder}/${Subject}/T1w/Diffusion. If you are using
your own diffusion model, be sure to take into account the gradient
nonlinearity effects on the diffusion weighting and
DIC can run on CIFTI files; temporal concatenation in MELODIC now defaults
to using MIGP.
Thank you,
Yeun
On Fri, Jul 21, 2017 at 1:19 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
Hi Yeun,
I think you should use multi-run ICA+FIX given the relatively short r
For tractography of HCP data you would use the surfaces in
${StudyFolder}/${Subject}/T1w/fsaverage_LR32k/ and the diffusion data in
${StudyFolder}/${Subject}/T1w/Diffusion, which have the same ACPC rigid
registration to MNI space. If you want your tractography data to be aligned
with MSMAll
It is also worth noting that the HCP Pipelines output MSMSulc and MSMAll
surfaces only (FreeSurfer is worse at aligning function than MSMSulc with more
distortion).
Matt.
From:
>
on behalf of Timothy Coalson
: TR = 800ms, 488 volumes, voxel size 2mm^3, for 2
runs (one AP, one PA phase encoding). Total time when concatenating the two
runs is about 13 minutes. Task fMRI runs are the same but shorter (300 volumes
for CARIT; 338 vol x 2 runs for an in-house task).
On Thu, Jul 20, 2017 at 5:38 PM, Glasser
e fMRI scans (2 sets of rs-fMRIs and 2 sets of
task-fMRIs). Should we use hcp_fix_multi_run?
Thank you,
Yeun
On Wed, Jul 19, 2017 at 5:21 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
The latest of everything will work for most applications.
Peace,
M
ne
Don't recommend the parallel processing or the eddy_cuda?
On Tue, Jul 18, 2017 at 2:13 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
We really don’t recommend you do that. I would ask about the eddy_cuda on the
FSL or neurodebian lists.
Peace,
Matt
Is the hcp_fix script in http://www.fmrib.ox.ac.uk/~steve/ftp/fix.tar.gz (the
latest release - version 1.065) the correct one to use, then?
On Wed, Jul 19, 2017 at 5:15 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
I wouldn’t worry about that. Those m
#
${HOME}/pipeline_tools/fix1.06a/melodic -i $fmri -o
${fmri}.ica/filtered_func_data.ica -d -250 --nobet --report --Oall --tr=$tr
---
Or should I be using the old melodic?
On Wed, Jul 19, 2017 at 5:05 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
What is this in r
What is this in reference to?
Peace,
Matt.
From:
>
on behalf of Yeun Kim >
Date: Wednesday, July 19, 2017 at 7:04 PM
To:
What kind of resolution are you looking to do and for what purpose?
Peace,
Matt.
From:
>
on behalf of Sebastien Hetu >
Date: Wednesday, July 19, 2017 at 3:28 PM
ail). After
that, we downsample them on the surface to the more sensible resolution.
Tim
On Mon, Jul 17, 2017 at 6:44 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
No that would be a massive oversampling of the data. The data are acquired at
2mm isot
outh Euclid Ave.Tel: 314-747-6173<tel:(314)%20747-6173>
St. Louis, MO 63110Email: mha...@wustl.edu<mailto:mha...@wustl.edu>
From:
<hcp-users-boun...@humanconnectome.org<mailto:hcp-users-boun...@humanconnectome.org>>
on behalf of Yeun Kim <yeun...@gmail.com<mailt
nal folding
detail (even though 32k surfaces still have very good folding detail). After
that, we downsample them on the surface to the more sensible resolution.
Tim
On Mon, Jul 17, 2017 at 6:44 PM, Glasser, Matthew
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
No that
What version of the software is this and what scanner? Also, what are the
sequence parameters?
Peace,
Matt.
From:
>
on behalf of A R >
Date: Tuesday, July 18,
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