[R] Repeated measures lme or anova
hadley wickham
h.wickham at gmail.com
Sun Jul 6 16:20:30 CEST 2008
On Sun, Jul 6, 2008 at 7:46 AM, Martin Henry H. Stevens
<HStevens at muohio.edu> wrote:
> Hi John,
> 1. I do not know why you remove the intercept in the lme model, but keep it
> in the aov model.
> 2. The distributional assumptions are shot --- you can't run any sort of
> normal model with these data. You might consider some sort of binomial
> (metabolite detected vs. not detected).
> Hank
Following along with Hank's suggestion:
names(df) <- tolower(names(df))
library(reshape)
cast(df, drug1 + drug3 + drug2 ~ ., function(x) sum(x > 0.1))
gives:
drug1 drug3 drug2 (all)
1 0 0 0 9
2 0 0 1 9
3 0 1 0 4
4 0 1 1 3
5 1 0 0 0
6 1 0 1 0
7 1 1 0 0
8 1 1 1 0
So drug 3 has the most effect, drug 3 about half as much, and drug 2
appears to have no effect.
Looking at the mean metabolite levels, conditional on the presence of
metabolite, gives a slightly richer story:
cast(df, drug1 + drug3 + drug2 ~ ., function(x) mean(x[x > 0.1]))
drug1 drug3 drug2 (all)
1 0 0 0 471.6033
2 0 0 1 535.9811
3 0 1 0 217.6300
4 0 1 1 393.3667
5 1 0 0 NaN
6 1 0 1 NaN
7 1 1 0 NaN
8 1 1 1 NaN
So under drug 2 doesn't affect the number of people with a detectable
amount of metabolite, but does affect the levels. (Although you do
need to bear in mind that the values will be more variable when there
are a few patients). You'd probably also want to look at this on a
patient by patient basis to ensure that those responders are the same
people.
For this sort of data, I'd encourage you to try Mondrian
(http://rosuda.org/mondrian) for some interactive graphical
exploration.
Hadley
--
http://had.co.nz/
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