mritotal joe_mri.mnc mri2tal_lin.xfm
tirmi joe_mri.mnc joe_trans.mnc -mrital_xfm mri2tal_lin.xfm mri2petThe ouput is the file mri2pet.xfm
mincresample -like joe_hiresPET.mnc -transformation mri2pet.xfm -zstart -18.5 -step 1 1 2 -nelements 256 256 60 joe_mri.mnc joe_MRIinPET.mncThe joe_hiresPET.mnc volume has been generated by summing up all dynamic frames to obtain a high-resolution PET volume, and by resampling along the axial dimension to obtain a slice thickness equivalent to that of the MRI volume. Such volume is best suited to estimate the performance of the registration procedure. Here, the output resampled volume consists of sixty 2-mm slices. The starting position of the resampled MRI volume (-18.5 mm) has been chosen such that it is exactly twice the PET axial resolution (6 mm FWHM for the PC-2048) lower than the centre of the first PET slice, ensuring enough data for the simulation of the first PET slice. As a rule-of-thumb, for a simulation of the complete 15-slice volume, the number of MRI slices should not be smaller than 15 x (6/zstep_of_MRI) + 2 x (12/ztep_of_MRI), which is 57 in our ex. here (and we chose 60). At that stage, you should verify the accuracy of the registration procedure by loading joe_hiresPET.mnc and joe_MRIinPET.mnc in REGISTER, and make sure there is a good alignment of these 2 volumes).
pvc_nlfit -nonlin joe_mri.mnc -linear_xfm mri2tal_lin.xfm mri2tal_nl.xfmThe output is mri2tal_nl.xfm
mincresample -like /avgbrain/brain/images/icbm_template_1.00mm.mnc joe_mri.mnc -transformation mri2tal_lin.xfm joe_mri_stx.mncThe MRI volume in Talairach space in then classified using tag cleaning:
classify_clean joe_mri_stx.mnc joe_stx-clas.mnc
stx_segment mri2tal_nl.xfm mri2tal_lin.xfm joe_stx-clas.mnc \ joe_labels_stx.mnc
pvc_transform_labels joe_labels_stx.mnc mri2pet.xfm mri2tal_lin.xfmGTM_002 GTM_006 GTM_010 GTM_014 TAC_003 TAC_007 TAC_011 TAC_015 GTM_003 GTM_007 GTM_011 GTM_015 TAC_004 TAC_008 TAC_012 GTM_004 GTM_008 GTM_012 TAC_001 TAC_005 TAC_009 TAC_013joe_hiresPET.mnc joe_labels_inPET.mnc -label FDOPA_labels.datThe tracer-dependent translation file FDOPA_labels.dat has been derived from /usr/local/mni/data/PVCcorrect/standard_labels.dat
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Simulation of regional spread functions (RSF) for the different tissue components present in the segmented MRI volume in PET native space:
3. PET simulation pvc_petsim joe_labels_inPET.mnc joe_pet.mnc \ joe_RSF.mnc joe_ROI.mnc -label FDOPA_labels.dat
4. Data extraction Extraction of time-activity curves (TAC's) from the real PET images, and the geometric transfer matrices (GTM's) from the simulated (RSF) images:pvc_extract_matrix joe_RSF.mnc joe_pet.mnc joe_ROI.mnc \ GTM_ TAC_ listROI -label FDOPA_labels.datThe output are a bunch of GTM_??? and TAC_??? files. By default, the program will generate 15 of each for the PC-2048 system: GTM_001 and TAC_001 for the first slice, GTM_002 and TAC_02 for the 2nd slice, etc... GTM_001 GTM_005 GTM_009 GTM_013 TAC_002 TAC_006 TAC_010 TAC_014
>> pvc('TAC_','GTM_','../joe_pet.mnc')After computing the inverse matrices and the resulting PVC TAC's, the program will launch a TK/Tcl program that allows to perform 3-D averaging across slices (see next paragraph for more info).
tac -cortac cortac -obstac obstac -roilist listROI -tacdir .where listROI is one of the output from pvc_extract_matrix. The -tacdir option indicates where the output data from pvc_extract_matrix are located.
A more detailed pic (45K) is available by clicking here or on the above pic
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Comments or suggestions? Please contact:
<olivier@bic.mni.mcgill.ca>
last updated: Jan. 1st, 1999