Thank you very much!
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Researcher
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: "Hodge, Michael"
Date: Thursday, May 30, 2019 at 7:24 AM
To: "Harms, Mich
Dear Experts,
I would like to access the item-level data for the NIH Emotion battery of the
young adult release.
How can I do that?
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Researcher
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.
I did and actually some subjects worked, but not these ones: 101006 159441
926862 927359 942658
I still get a “cannot find file” error (10.4.5).
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Researcher
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.
942658
Is that normal?
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Researcher
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: "Harms, Michael"
Date: Wednesday, May 15, 2019 at 9:31 AM
To: Leona
for this? These are the IDs: '127226' '130114' '169040'
'329844' '908860' '971160'
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5
)
this = read_gifti_file_standalone(varargin{1},giftistruct);
Error in ciftiopen (line 31)
cifti = gifti([tmpfile '.gii']);
Error in fix_3_clean (line 46)
BO=ciftiopen('Atlas.dtseries.nii',WBC);
}^H
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu
in ciftiopen (line 31)
cifti = gifti([tmpfile '.gii']);
Error in fix_3_clean (line 46)
BO=ciftiopen('Atlas.dtseries.nii',WBC);
}^H
Would you have any thoughts on this?
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto
the TaskfMRIAnalysis
scripts to get my “activations”.
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: "Harms, Michael"
Date: Monday, February 25,
.
A related question I would have is what filter you would recommend for task
data. My intention is to use a GLM on the cleaned data, so is 2000 (linear
detrending) ok, since then a lower high-pass will be applied in the GLM step?
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab
Dear Matt,
Looks like I really need to improve my linear algebra.
Thank you very much!
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: "Glasser, Matthew"
by rerunning the surface preprocessing step.
Would you have any suggestions?
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5
alternative suggestions on how to handle multi-session data
at the group level?
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: Leonardo Tozzi
Date: Wed
It worked!
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: "Glasser, Matthew"
Date: Tuesday, January 8, 2019 at 3:52 PM
To: Leonard
ant here and where I should point this variable: I am
using the ciftiopen and ciftisave functions to open and read cifti files. Would
you have any suggestion on what the FSL_FIX_CIFTIRW variable should be so that
I can write the cleaned timeseries?
Thank you very much,
Leonardo Tozzi, MD,
artifacts, then
run MELODIC ICA on the cleaned data at the group level to get some group
components and then get the individual components with double regression?
Or is there some problem you see in running an ICA after an ICA?
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab
data. Also, I would probably need to retrain the classifier, since we are
conducting our experiment at a different site and on a GE magnet, correct?
I would appreciate any pointers on how to best proceed with this matter.
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral
.
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
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HCP-Users@humanconnectome.or
make the same call as before, with the –avoid flag for the CSF but I
guess I would still at least need to input the GrayOrdinates.txt which is still
a list of seeds (-x option). How would I obtain the seed list for the
grayordinates?
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab
and Connectomes/GrayOrdinates.txt ?
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: Timothy Coalson
Date: Friday, November 9, 2018 at 5
matrix by taking the
upper triangle. I think it should track from all my ROIs to all my ROIs.
Concerning wb_command -probtrackx-dot-convert, it requires a few inputs but I
am not sure what files to use.
I hope this adds more information, thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab
/tfMRI_EMOTION_LR
. Would this be acceptable, for example in the case in which I were to
download only the task data from your release (so I wouldn’t have the original
T1s)? If not, is there another approach you would recommend?
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral
or any other suggestion to check the
positioning of the seeds and the tractography results?
Thank you very much,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: Sta
will try going through the steps and see if I manage to make it work.
Thank you,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
From: Stamatios Sotiropoulos
Date: Wednesday, Octo
subject’s parcellation
into a series of NIFTI files in native/standard space and input these as ROIs
into probtrackx? In this case, could you recommend the correct series of
workbench commands? I am also open to other software recommendations besides
the FSL suite.
Thank you very much,
Leonardo
for me or have any tips on achieving what I
am trying to do in an optimal way.
Thank you very much.
Yours sincerely,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5
displayed in the
workbench? Are they being “carried over” as labels that do not actually
correspond to any greyordinates? Should I be worried that these “Phantom
labels” might affect my analyses?
Thank you very much.
Yours faithfully,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
something strange about them.
Thank you very much.
Yours faithfully,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
___
HCP
be an acceptable solution.
Thank you very much.
Yours faithfully,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto...@stanford.edu<mailto:lto...@stanford.edu> | (650) 5615738
___
HCP-Users mailing li
provide some pointers so make this edit as small as possible (I would
like to avoid “shuffling” my scans, bvals and bvecs before launching the
preprocessing).
Thank you very much.
Yours faithfully,
Leonardo Tozzi, MD, PhD
Williams PanLab | Postdoctoral Fellow
Stanford University | 401 Quarry Rd
lto
AP and PA and for each we have a
file with 81 and one with 83 directions. So, the number of volumes in
Pos_Neg.nii.gz seems to be correct (81+83+81+83=328), but the index file is
somehow truncated.
Would anyone have some insight in why that could be the case?
Thank you very much.
Yours faithfully,
Leon
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