Duke-UNC Brain Imaging and Analysis Center
BIAC Forums | Profile | Register | Active Topics | Members | Search | FAQ
 All Forums
 Support Forums
 Analysis Software Support
 FSL Repeated Measures ANOVA?

Note: You must be registered in order to post a reply.
To register, click here. Registration is FREE!

Screensize:
UserName:
Password:
Format Mode:
Format: BoldItalicizedUnderlineStrikethrough Align LeftCenteredAlign Right Horizontal Rule Insert HyperlinkInsert EmailInsert Image Insert CodeInsert QuoteInsert List
   
Message:

* HTML is OFF
* Forum Code is ON
Smilies
Smile [:)] Big Smile [:D] Cool [8D] Blush [:I]
Tongue [:P] Evil [):] Wink [;)] Clown [:o)]
Black Eye [B)] Eight Ball [8] Frown [:(] Shy [8)]
Shocked [:0] Angry [:(!] Dead [xx(] Sleepy [|)]
Kisses [:X] Approve [^] Disapprove [V] Question [?]

 
Check here to subscribe to this topic.
   

T O P I C    R E V I E W
Jeff_Browndyke Posted - Oct 14 2013 : 2:45:35 PM
I've been working with FSL basic TBSS scripts with relative success, but being a FSL novice I've been using the processing recipe here: http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/tbss/UserGuide

This guide, however, only provides help on constructing design.mat and design.con files for basic 2-sample t-tests. I'm trying to figure out how to construct a repeated measures x 2 sample ANOVA (i.e., group x time) for 12 patients and 12 controls to examine differences in FA between baseline and 6wk post-op and their interaction. Does anyone know how to code this sort of model in FSL and the required contrasts? I looked at the code in the design.mat and design.con files for the 2-sample and that code seems pretty simple, but I'm not certain what to do about a repeated measures ANOVA where within- and between-variance needs to be computed.

BTW - I'm processing all four timepoints together to obtain an overall study specific mean FA skeleton and have named the files alphabetically to indicate the groups by timepoints (e.g., Controls Tp1 = A0...n; Patients Tp1 = B0...n; Controls Tp2 = C0...n; Patients Tp2 = D0...n).

Thanks for any help, tips, pointers, etc.

Jeff
4   L A T E S T    R E P L I E S    (Newest First)
Jeff_Browndyke Posted - Oct 14 2013 : 3:37:48 PM
Cool. Thanks again!
petty Posted - Oct 14 2013 : 3:35:15 PM
no, you keep using randomise .. Set-up your glm with Glm, but now you'll need design.mat, design.con and design.fts

So add this flag to your randomise line:
	-f <design.fts>	f contrasts file

Jeff_Browndyke Posted - Oct 14 2013 : 3:29:38 PM
Thanks, Chris! I'm assuming that I cannot use "randomize?" The TBSS script line I've been using for the 2-sample procedure with TFCE correction and 500 permutations is:

randomise -i all_FA_skeletonised -o tbss_FA -m mean_FA_skeleton_mask -d design.mat -t design.con -n 500 --T2 -V

Regards,
Jeff
petty Posted - Oct 14 2013 : 3:20:11 PM
Hey Jeff,

You can should be able to open the Glm design tool ( "Glm" ) and set-up an 2x2 anova identical to the one described here:
http://fsl.fmrib.ox.ac.uk/fsl/fsl4.0/feat5/detail.html#ANOVA2factors2levels

You just have to make sure you are concatenating your subjects in the same order as you have them defined in the Glm

BIAC Forums © 2000-2010 Brain Imaging and Analysis Center Go To Top Of Page
This page was generated in 0.4 seconds. Snitz Forums 2000