Differences between revisions 1 and 2
Deletions are marked like this. Additions are marked like this.
Line 1: Line 1:
Describe FsFastFunctionalConnectivityWalkthrough here. ===work in progress...===

==About==
Walkthrough: How to use FsFast and fcseed-sess for functional connectivity analysis

 [[http://surfer.nmr.mgh.harvard.edu/pub/docs/freesurfer.fsfast.ppt|Functional Analysis with FS-FAST]]

*STEP 1: Unpack Data into the FSFAST Hierarchy using "unpackscmdir"

[[https://surfer.nmr.mgh.harvard.edu/fswiki/unpacksdcmdir| unpacksdcmdir]]

1.QA Check after unpacking
A - Check unpacked data (time points, # of slices ..etc)
B - Check FSFAST hierarchy in session folder

*STEP 2: reconstruct anatomical data using
# Reconstruction – Anatomical using "recon-all –all"
1.Set SUBJECTS_DIR
2.QA Check
A - Check talairach transformation
B - Check skull strip, white matter & pial surface
C - Re-run "recon-all" if edits are made
D - Check hierarchy of reconstructed anatomical data
[[https://surfer.nmr.mgh.harvard.edu/fswiki/recon-all recon-all]]

1.Make FSFAST basic hierarchy (only if data are not unpacked in FSFAST hierarchy)
2.Link to FreeSurfer anatomical analysis
A - Make ‘subjectname’ file in the session directory to link a subject's functional & structural data
3.Create a sessid file (text file with list of your sessions)in your Study DIR.
4.Create a Stimulus Schedule (Paradigm file) in bold folder (A "paradigm" file is a record of which stimulus was presented when & for how long. Each paradigm file has four columns:
A - Stimulus onset time (sec)
B - Condition ID code (0, 1, 2, ...)
C - Stimulus Duration (sec)
D - Stimulus Weight (usually 1)


*STEP 3: Pre-process your bold data using preproc-sess
[[http://surfer.nmr.mgh.harvard.edu/fswiki/preproc-sess preproc-sess]]
# Preprocessing of fMRI Data ()
preproc-sess -s <subjid> -fwhm <#>
1.By default this will do motion correction, smoothing & brain masking
2.Quality Check (plot-twf-sess)
3.Examine additions to FSFAST hierarchy (in each run of bold dir):
- f.nii (the raw data)
- fmc.nii (motion corrected-MC)
- fmcsm5.nii (MC & smoothed)
- fmc.mcdat - text file with the MC parameters (AFNI)
- mcextreg.bhdr - binary mask of the brain
# Function-Structure Registration
View unregistered
tkregister-sess -s <subjid> -regheader)
Run automatic registration
spmregister-sess -s <subjid>
Check automatic registration
tkregister-sess -s <subjid>
A - Make edits if needed using scale as the last resort
Check talairach registration
tkregister2 --s <subjid> --fstal --surf


*STEP 4: Use fcseed-sess to generate time-course information for your chosen seed region (as well as nuisance variable signal).


*STEP 5: Use mkanalysis-sess to setup an analysis for your FC data



*STEP 6: Use selxavg3-sess to run the subject-level analysis



*STEP 7: Use mri_glmfit or selxavg3-sess to run a group-level analysis

===work in progress...===

==About== Walkthrough: How to use FsFast and fcseed-sess for functional connectivity analysis

*STEP 1: Unpack Data into the FSFAST Hierarchy using "unpackscmdir"

unpacksdcmdir

1.QA Check after unpacking A - Check unpacked data (time points, # of slices ..etc) B - Check FSFAST hierarchy in session folder

*STEP 2: reconstruct anatomical data using # Reconstruction – Anatomical using "recon-all –all" 1.Set SUBJECTS_DIR 2.QA Check A - Check talairach transformation B - Check skull strip, white matter & pial surface C - Re-run "recon-all" if edits are made D - Check hierarchy of reconstructed anatomical data https://surfer.nmr.mgh.harvard.edu/fswiki/recon-all recon-all

1.Make FSFAST basic hierarchy (only if data are not unpacked in FSFAST hierarchy) 2.Link to FreeSurfer anatomical analysis A - Make ‘subjectname’ file in the session directory to link a subject's functional & structural data 3.Create a sessid file (text file with list of your sessions)in your Study DIR. 4.Create a Stimulus Schedule (Paradigm file) in bold folder (A "paradigm" file is a record of which stimulus was presented when & for how long. Each paradigm file has four columns: A - Stimulus onset time (sec) B - Condition ID code (0, 1, 2, ...) C - Stimulus Duration (sec) D - Stimulus Weight (usually 1)

*STEP 3: Pre-process your bold data using preproc-sess http://surfer.nmr.mgh.harvard.edu/fswiki/preproc-sess preproc-sess # Preprocessing of fMRI Data () preproc-sess -s <subjid> -fwhm <#> 1.By default this will do motion correction, smoothing & brain masking 2.Quality Check (plot-twf-sess) 3.Examine additions to FSFAST hierarchy (in each run of bold dir): - f.nii (the raw data) - fmc.nii (motion corrected-MC) - fmcsm5.nii (MC & smoothed) - fmc.mcdat - text file with the MC parameters (AFNI) - mcextreg.bhdr - binary mask of the brain # Function-Structure Registration View unregistered tkregister-sess -s <subjid> -regheader) Run automatic registration spmregister-sess -s <subjid> Check automatic registration tkregister-sess -s <subjid> A - Make edits if needed using scale as the last resort Check talairach registration tkregister2 --s <subjid> --fstal --surf

*STEP 4: Use fcseed-sess to generate time-course information for your chosen seed region (as well as nuisance variable signal).

*STEP 5: Use mkanalysis-sess to setup an analysis for your FC data

*STEP 6: Use selxavg3-sess to run the subject-level analysis

*STEP 7: Use mri_glmfit or selxavg3-sess to run a group-level analysis

FsFastFunctionalConnectivityWalkthrough (last edited 2024-01-16 14:11:01 by DougGreve)