Hi all,
I am working on a pretty complex dataset and am just wondering if anyone knows whether or not a PLS analysis would be appropriate / could work. The data consists of 2 conditions (rest vs. active), 2 participant groups (control vs feedback), 2 sessions ( 1 vs. 2), 14 participants total (7 per group), 15 frequency bands, and 3160 possible Functional Connections (based on a coherence analysis).
I am just wondering if there is anyway to use a PLS to test differences in Functional connectivity between conditions and groups, across sessions.
I have done a PLS before using a 2 (conditions) x 19 (participants) x 15 (frequency bins) x 3160 neural connections. That one was more straight forward. However I have a feeling that throwing in the groups and sessions makes a PLS not usable. If anyone has any insight or suggestions on how to analyze this data that would be great.
Thanks a lot!
-Ron
Hi all,
I am working on a pretty complex dataset and am just wondering if anyone knows whether or not a PLS analysis would be appropriate / could work. The data consists of 2 conditions (rest vs. active), 2 participant groups (control vs feedback), 2 sessions ( 1 vs. 2), 14 participants total (7 per group), 15 frequency bands, and 3160 possible Functional Connections (based on a coherence analysis).
I am just wondering if there is anyway to use a PLS to test differences in Functional connectivity between conditions and groups, across sessions.
I have done a PLS before using a 2 (conditions) x 19 (participants) x 15 (frequency bins) x 3160 neural connections. That one was more straight forward. However I have a feeling that throwing in the groups and sessions makes a PLS not usable. If anyone has any insight or suggestions on how to analyze this data that would be great.
Thanks a lot!
-Ron
Hi Ron - you can certainly use PLS for this, but you may have to run a few analyses to get an idea of what you have. I might suggest something like:
1) run the whole thing to get a feel for the number of stable effects
2) if #1 yields good results, break it down along a reasonable dimension (e.g., group) to see what comes out. You can think of this as a sort of post-hoc test
3) consider putting in apriori contrasts of interest to evaluate specific effects (non-rotated PLS)
I'd be interested to hear how this goes, so please let me know!
cheers
Randy
Baycrest is an academic health sciences centre fully affiliated with the University of Toronto
Privacy Statement - Disclaimer - © 1989-2024 BAYCREST HEALTH SCIENCE. ALL RIGHTS RESERVED