History of AFNI updates  

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July 14, 2020 11:54AM
Hi Gang,

I'm very interested in modeling trial as a random factor. Do I understand correctly from the bioRxiv paper that the implementation would be to use 3dREMLfit with one regressor for each trial, and then use 3dLMEr with each trial as an input file for one massive model? As in (following your example):

3dLMEr -prefix LME \
...
Subj Emotion Trial InputFile \
s1 pos T1 s1_decon+tlrc'[1]' \
s1 pos T2 s1_decon+tlrc'[2]' \
s1 pos T3 s1_decon+tlrc'[3]' \
...
s1 neu T1 s1_decon+tlrc'[x]' \
s1 neu T2 s1_decon+tlrc'[y]' \
...
s2 pos T1 s2_decon+tlrc'[1]' ...

Thank you,
nmuncy
Subject Author Posted

Should BOLD response be modeled at the trial level?

gang May 28, 2020 04:14PM

Re: Should BOLD response be modeled at the trial level?

ptaylor May 28, 2020 04:40PM

Re: Should BOLD response be modeled at the trial level?

gang May 28, 2020 07:39PM

Re: Should BOLD response be modeled at the trial level?

ptaylor May 29, 2020 11:26AM

Re: Should BOLD response be modeled at the trial level?

nmuncy July 14, 2020 11:54AM

Re: Should BOLD response be modeled at the trial level?

gang July 15, 2020 09:13AM