Derek Jones suggests at least 31 diffusion directions, and 1 bzero (T2-weighted) volume for every 6 diffusion directions. I would also suggest 2mm isotropic voxels and a bvalue of 2000 or 3000. If you have access to it, you could also use multiband to reduce scanning time.
Thanks a lot for the suggestions! In fact we have a problem that we cannot increase the number of slices >43. As I want a 2mm slice thickness, this means that we cannot cover the entire brain. I do not see a logical reason for this. Do you have the same problem? Or any idea to overcome this limitation?
Thanks a lot for your answer! I would be very helpful if I could see the image quality that you got, so I can get an idea whether our image quality is in line with that of other centers !
the visual impression of these scans is comparable with the quality of our images, so I am happy about this
one question: you also have 5 b0 images, this seems to be a particularity of GE as I did not know this from Siemens or Philips. Is this really useful and improves the quality of the fit ?
Is there a reason you chose a b-value of 1000 (rather than 2000 or 3000)?
Indeed, that article by Derek Jones is full of great advice.
If you have time, you may want to consider 10 b0 volumes (it has been suggested that 1 bo volume for every 6 directions is optimal).
Based on your in-plane resolution, I assume your matrix is something like 512x512? If so, then changing it to 256 x 256 should produce isotropic voxels.
Is your scanner a 750 or 750w? Did you use a GE 32 channel head coil or a NOVA head coil?
For a 1.5T, I would suggest 32 directions at a single bvalue of 1000 with 2 bzero volumes, and spatial resolution of 2.5mm. If you have a research key, then you can acquire isotropic voxels, and also interleave the bzero volumes. Which head coil and console DV software version are you using?
4.7 is the AW. What version is on the console (e.g. DV28)?
A research key is something you apply to GE for. It opens up the scanner to research mode (by default the scanner is in clinical mode) and therefore allows you access to hundreds of CVs (control variables) that clinical mode does not show.