'$' - indicates shell commands

'dir' - refers to the directory where the study data is found (ex. /jet/aguirre/CrossModal)

'new subject' - the subject you are currently analyzing (ex. X111111X)

'old subject' - a subject that has been analyzed previously (ex. X000000X)

Follow steps found on Preprocessing wiki

Use /jet/aguirre/CrossModal/PrepScripts/VBPs/'old subject'.vbp & /jet/aguirre/CrossModal/PrepScripts/VBPs/Stock_CMP_Prep_new.vbp

[output: fAnisotropy and Mean Diffusivity]

$cd 'dir'/'new subject'/DTI

If there are 2 DTI scans:

$mkdir 'dir'/DTI/combined_DTI
$cp 00*/* combined_DTI

If there is only 1 DTI scan:

$mkdir 'dir'/DTI/one_DTI
$cp 00*/* one_DTI

Open Matlab [See Also http://alliance.seas.upenn.edu/~pauly2/wiki/index.php?n=Main.DTITools for additional help]

>cd(‘Volumes/170.212.110.245’)
If there are 2 scans: 
	>cd(/Aguirre/CrossModal/[subject]/DTI/combined_DTI/
If there is only 1 scan: 
	>cd(/Aguirre/CrossModal/[subject]/DTI/one_DTI/
>dti_ui  **dialog box will open**
    * in bottom of box type “-bgthresh 50 -md”
Click button “DICOM ->Analyze DTI"
Check to make sure you are in 'dir'/'new subject'/DTI/[combined or one_DTI]
Click “All”
When all images are highlighted in blue → Click “Done”
   *this produces files “ep_b1000#(0-# of directions) and “ep_b0…” for ea. DTI scan

[Pause - approx. 10 minutes]

Now follow the following steps:
1) Select ONLY the "b0" images in order (ex. ep_b0-0012… and ep_b0-0013…)
2) Select the remaining b1000 files for the 1st scan in order (ex. ep_b1000#0-0012…, ep_b1000#1-0012…,…) 
   * If there is only one scan all of the files will be selected when you have completed this step
3) Select remaining b1000 files for the 2nd scan (in order) etc. (Only needed if there are 2 scans)
4) Select “Done”
5) Set your path to /jet/aguirre/CrossModal/ScriptsDTI
	If 2 scans: select “HUP_M1_N12_b1000_R2.scheme.txt”
	If 1 scan: select “HUP_M1_N12_b1000.scheme.txt”
	* These files can be copied to your directory for use for other studies
6) Click “Done”
7) Change directory to 'dir'/"new subject"/DTI/ and click the “analyzed” folder (located on the RIGHT side of the window)
8) Click “Done”
9) When prompted for (optional mask) click “Done”

[Pause: at this point the program will run for approximately 1 hr.]

If you receive an error message that the command “analyzedti” did not run (due to inability to access camino path)

$cd 'dir'/'new subject'/DTI/[combined or one_DTI]
If 2 scans: $analyzedti imagelist.txt 'dir'/'new subject'/DTI/analyzed/'dir'/ScriptsDTI/HUP_M1_N12_b1000_R2.scheme.txt 
If 1 scan: $analyzedti imagelist.txt 'dir'/'new subject'/DTI/analyzed/'dir'/ScriptsDTI/HUP_M1_N12_b1000.scheme.txt 

!! Beware: Due to down sampling, this step causes a large drop in resolution. This is not being done with our CrossModal data!!

$cd 'dir'/PrepScripts/CoRegFaMd_Scripts
$cp “old subject”_CoRegNorm_FaMd.vbp “new subject”_CoRegNorm_FaMd.vbp
$emacs “newsubject”_CoRegNorm_FaMd.vbp
	replace string: “old subject” with “new subject”
	*Check line 34: .tes files are named correctly?
$vbprep “newsubject”_CoRegNorm_FaMd.vbp
	*output will be “nfa_CoReg.cub in Anatomy/

To view “nfa_CoReg.cub” load as you would for functional data and use a range of 1.0 to 0.0

(Warping standard MNI brain to subject T1 space)

Open matlab

>cd ‘dir’/'new subject'/DTI/norm/t1
>dti_ui
	1) Click Step 1 (HUP DTI DICOM Conversion)
	2) Click up to 'new subject'/Anatomy/raw/*MPRage
	3) Click All
	4) Click Done
	** window closes

At this point you are finished using Matlab

$cd 'dir'/'new subject'/DTI/norm/t1
$mv tfl3d1*.hdr tfl3d1.hdr
$mv tfl3d1*.img tfl3d1.img
$ln –s /home/pcook/prasad/ch2.hdr ch2.hdr
$ln –s /home/pcook/prasad/ch2.img ch2.img
$cd 'dir'/ScriptsDTI/
$cp mvsn.sh ../'new subject'/DTI/norm/t1/.
$cd 'dir'/'new subject'/DTI/norm/t1
$./mvsn.sh &

[Pause: this will take about an hour to process]

The output will be inside the t1 folder and will be several ch2* files

!! Continue ONLY after DTT T1 files are made (mvsn.sh program)

$cd ‘dir’/subject/DTI/norm/b0

If 2 scans:

$cp ‘dir’/subject/DTI/combined_DTI/ep_b0-(1st scan)*.img b0_1.img
$cp ‘dir’/subject/DTI/combined_DTI/ep_b0-(1st scan)*.hdr b0_1.hdr
$cp ‘dir’/subject/DTI/combined_DTI/rep_b0-(2nd scan)*.img b0_2.img
$cp ‘dir’/subject/DTI/combined_DTI/rep_b0-(2nd scan)*.hdr b0_2.hdr
$cd 'dir'/ScriptsDTI/
$./mnitob0.sh 'new subject' &

If 1 scan:

$cp ‘dir’/subject/DTI/one_DTI/ep_b0-(scan)*.img b0.img
$cp ‘dir’/subject/DTI/one_DTI/ep_b0-(scan)*.hdr b0.hdr
$cd 'dir'/ScriptsDTI/
$./mnitob0_norepeat.sh ‘subject’ &

[Pause: Makes occipital-thalamus* analyze files, t1tob0* files and xMNI* files]

$cd ‘dir’/ScriptsDTI/ $./vistob0.sh ‘new subject’ & $./AvgV1tob0.sh 'new subject' &

$'dir'/'new subject'/DTI/norm/b0

$snap

Here a SNAP window will open

Click File - Load Data - Greyscale Image or [Ctrl+G]
Click Browse
Select "t1tob0_symmAregistered.nii"
Click OK
Click NEXT
Type "RPI" in the "RAI Code" box.
Click NEXT
Click FINISH
Click DON'T RESTORE
Under the IRIS Toolbox in the upper lefthand corner, click the paintbrush tool

Reduce the brush size to 6 using the scroll bar under "Tool Options" (It will be set at 8)
Check the box below the size box called "Isotropic"
Using sagittal view, in the upper right window, highlight the posterior portion of the corpus collosum as seen here... 

Click FILE - SAVE DATA - SAVE SEGMENTATION IMAGE
Click Browse and go to the subject's tracking folder (../tracking)
Click into the Filname box at the bottom of the window and add the filename "genu.mha" to the end of the path
Click OK
Click SAVE
Close the SNAP window

$./track_vis_thalamus.sh ‘new subject’ &

(Building Paraview state for future viewing)

Open Paraview
Open ‘dir’/’new subject’/DTI/norm/tracking/fa_rgb.mhd
Click [Apply]
Click [Slice icon] *use x normal*
Unclick [show plane]
Click [Apply]
Click [Display]
Unclick [Map Scalars]
Open ‘dir’/’new subject’/DTI/norm/tracking/AllVisAreas-thalamus-thr0_b0.mha
Click [Apply]
Click [Threshold icon]
Set lower and upper thresholds to 1
Click [Apply]
Click [Display]
Reduce Opacity to 0.5
	** Now you can view the visual areas**
In Pipeline Browser click on ‘AllVisAreas-thalamus-thr0_b0.mha’
Click [Threshold icon]
Set lower and upper thresholds to 2
Click [Apply]
** Now you can view the thalamus**
Click [Display]
Reduce Opacity to 0.5
In Pipeline Browser click on ‘fa_rgb.mhd’
Click [Slice]
Click [Z normal]
Move slice to near the bottom of the thalamus by clicking and dragging
Deselect [show plane]
Click [apply]
Click [display]
Deselect [map scalars]
Click [File menu/ save state]
Select ‘dir’/’new subject’/DTI/norm/tracking 
	** Careful!! The directory is maintained from the previous time a state was saved**
Filename: Paraview State [subject initials]
Click OK
	Holding (control) while dragging [zoom]
	Holding (shift) while dragging spins on axis
To load tracks 
Click Open
Open ‘dir’/’new subject’/DTI/norm/tracking/AllVisAreas-thalamus-thr0-endpoints.vtk
Click Apply
	To open a previously built state
Click [file menu / Load state]
Click