Hi Mark, > Thanks for your response - I guess I am interested in the > result of an > F-test across the three samples so it sounds like it will > be worth a try. Sure, but bear in mind that it will only tell you where are the significant changes across the 3 groups, so you will still need to run the post-hoc t-tests on each pair of groups to determine what's "driving" these results. > With regards to what my question is: it's partially > answered by my results > from the three 2-way analyses. I see that illness1 vs > controls shows some > key reductions; illness2 vs controls shows more widespread > reductions and in > larger clusters; illness1 vs illness2 shows no differences > in either > direction. I'm interested in whether illness1 vs illness2 > really differ, as > the separate comparisons against controls implies that they > should, but a > direct comparison between them suggests that they don't. Yes, it can happen, this means that though illness2 seems more severe, this is not a significant effect. > (My numbers are > 20-30 in each group). Does method II assist in this? There is no way of knowing for sure, and if it does when you'll do the post-hoc t-test between illness1 and 2, this would be just because you have increased your DoFs, not because you would have asked a different question... Cheers, Gwenaelle > Rgds > > Mark > > > On 13/4/10 4:20 AM, "Gwenaëlle DOUAUD" <[log in to unmask]> > wrote: > > > Hi Mark and Jay, > > there is no good answer to this question I'm afraid. > > Say > > you've got two subjects in group A, 3 in B and 4 in C, > then both approaches > > are valid: > > Method I > > A B > > 1 0 > 1 0 > 0 1 > 0 1 > 0 1 > for the design.mat of the first > > A and B groups with > > 1 -1 (A-B) > -1 1 (B-A) > for the design.con > and then repeat > > for groups B and C, then groups A and C (which is what > you did Mark). > > Method > > II > > A B C > > 1 0 0 > 1 0 0 > 0 1 0 > 0 1 0 > 0 1 0 > 0 0 1 > 0 0 1 > 0 0 1 > 0 0 1 > for the > > design.mat of the 3 groups with > > 1 -1 0 (A-B) > -1 1 0 (B-A) > 0 1 -1 (B-C) > 0 -1 1 > > (C-B) > 1 0 -1 (A-C) > -1 0 1 (C-A) > for the design.con (t-tests) > and > > 1 0 1 0 0 > > 0 > for the design.fts (F-test, as many columns as there are > rows in your > > design.con, you just need to click in "F-tests" in the > Glm gui and then click > > in front of the two relevant "Contrasts" you have > already set up) > > So with > > Method II, you can also ask the question of where are > the changes *across the > > 3 groups* (F-test with the design.fts). You also get > an increase in DoF but, > > as Tom Nichols said, if it happens that group C for > instance has wildly > > smaller variance, you can get inflated significances > (or reduced power if it > > has wildly larger variance). > > So it depends on what your main question is, > > really. > > Hope this helps, > Gwenaelle > > > --- En date de : Lun 12.4.10, Mark > > Walterfang <[log in to unmask]> > a écrit : > > > De: Mark Walterfang > > <[log in to unmask]> > > Objet: Re: [FSL] FSLVBM GLM Setup > > À: > > [log in to unmask] > > Date: Lundi 12 avril 2010, 14h18 > > Hi all > > > > I'm in the > > same situation as Jay. I have three groups > > (illness1, illness2 > > and > > controls), all matched to each other. I've run three > > two-way analyses, > > > > which is pretty laborious and I'm pretty sure it's > not > > statistically > > ideal. > > What I can't work out is how to set up the design > matrices > > & > > contrasts in > > the way Jay describes, as the online manual for > Randomise > > > > doesn't really > > provide guidance here. Gwenaëlle, is this something > you > > can > > advise on? > > > > Thanks in advance, > > > > Mark Walterfang > > > > > > On 10/4/10 > > 12:29 PM, "Jay Ives" <[log in to unmask]> > > wrote: > > > > > I have 70 subjects in > > 4 groups and would like to test > > between individual > > > groups and > > combinations of the groups. Can someone > > please advise me how to set > > > up > > the design.mat and design.con files to do this? > > Thx > > > > > > WARNING: This > > message > > > originated from outside the > Northern/Melbourne/Western > > Health > > e-mail network. > > > The sender cannot be validated. Caution is > advised. > > > > Contact IT Services (+61 3 > > > ) 9342 8888 for more information. > > > > > > > > > > WARNING: This message originated from outside the > > Northern/Melbourne/Western Health e-mail network. The > sender cannot be > > validated. Caution is advised. Contact IT Services > (+61 3 ) 9342 8888 for more > > information. > > > Dr Mark Walterfang > Consultant Neuropsychiatrist > Neuropsychiatry Unit > Level 2, John Cade Building > ROYAL MELBOURNE HOSPITAL 3050 AUSTRALIA > T +61-3-93428750 > F +61-3-93428483 > E [log in to unmask] > W www.neuropsychiatry.org.au > > Research Fellow > Melbourne Neuropsychiatry Centre > University of Melbourne > Level 2 & 3, Allan Gilbert Building > 161 Barry St > CARLTON SOUTH 3023 AUSTRALIA > T +61-3-83441800 > F +61-3-93480469 > E [log in to unmask] > W www.psychiatry.unimelb.edu.au/mnc >