Dear FMRIBbbers,
I'd like to use flirt to align EPI data with a highres T1 volume
and maintain the resolution (number of slices, voxel size) of the original
EPI images.
I played around with flirt's options but it always resulted in a resampled
EPI_aligned.
Finally I tried using a dummy ref_volume (actually a copy of t2), like this
flirt -in lowres4d -ref lowres4d -applyxfm -init epi2anat.xfm -out
lowres4d_to_t1
but that didn't do the trick?
What am I missing?
cheers,
Hauke
+++%+++%+++%+++%+++%+++%+++%
Hauke R. Heekeren, MD
Lab of Brain and Cognition
NIH, NIMH/IRP
10 Center Dr
Room 1D80
Bethesda, MD 20892-1148
USA
voice: 001-301-402-1379
fax: 001-301-402-1370
email: [log in to unmask]
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