Apologiies for posting this again, I think it may have been missed the first time round.
I am working with multishell data with no reversed phase-encoding information, therefore cannot perform fsl topup. Is it still okay for me to use ACT in this instance? (I note there was some mention of this on the afdconnectivity page).
There’s a brief mention in the ACT documentation page, as well as the afdconnectivity page as you mentioned; but the better reference would probably be the ACT paper itself.
The fundamental assumption underlying ACT is that for any position in space, one can access both orientation information from the DWIs / diffusion model, and tissue information from segmentation of an anatomical image, and that this information corresponds to the same anatomical location. If the DWI EPI distortions are not corrected, this assumption can be grossly incorrect. So no, it’s generally advised against using ACT in this instance. Although tckgen won’t miraculously crash outright if it detects that your data have not been corrected by topup, using ACT may give a false perception of the accuracy of the resulting tracks, and could introduce errors that would not have been there if ACT were omitted.
Run whole brain tractography - select to retain 5 million tracts sufficient if using sift2 (10M ideal but takes years - could consider for smaller studies
instead. It’s already more accurate out of the box, even on highly corrected incredible quality HCP data (see, among others, this post), but if you’re facing a scenario where you’ve got no phase-encoding information, this becomes even more of a no-brainer. I’ve seen msmt_5tt response function outcomes in such scenarios before, and it’s not pretty.
Yep, no worries. But MSMT-CSD will be limited to 2 tissue types. To get 3 tissue types from such data, you’d need SS3T-CSD, which isn’t available publicly yet.
Sure, no worries again, but you may want to use the -fa option to dwi2response dhollander, and provide it with a slightly lower value than the default of 0.2. See this post, where success was shown on rat data: Multi-tissue CSD . The general advise for a mouse would be similar, but you’d probably have to be extra-careful about setting that parameter decently. Set it to a couple of values, and look at the -voxels output to see what makes sense (or doesn’t).