Hello,
I ran a second-level analysis for a seed-based correlation project on three cerebellar seeds (Dentate Nucleus Functional Territories). For the between-sources contrasts, I applied a unique effect for each seed. Examples of the contrasts I used are:
DMN DN Territory > Salience DN + Visual
DN: [1 0 0; 0 -1/2
0; 0 0 -1/2]
Salience DN Territory > DMN DN + Visual
DN: [-1/2 0 0; 0 1
0; 0 0 -1/2]
Visual DN Territory > DMN DN + Salience
DN: [-1/2 0 0; 0
-1/2 0; 0 0 1]
For reference, the source seed assignments are:
Source001: DMN DN
Source002: Salience DN
Source003: Visual DN
I also assigned an individual label for each unique effect analysis so that the data would remain organized.
I want to take the contrast maps generated from these analyses into SPM to perform a paired t-test on participant data, specifically to compare contrasts from their 3 T and 7 T resting-state scans.
However, when I check my directory, I see three contrast images per subject, for example:
CON_Subject001_compB001_001.nii
CON_Subject001_compB002_001.nii
CON_Subject001_compB003_001.nii
I’m unsure which of these contrast images I should export to SPM for my analysis- also are these automatically Fisher z-transformed or would I need to convert them. Any help would be appreciated!
Thanks,
Zach
