In article <[EMAIL PROTECTED]>,
[EMAIL PROTECTED] (Donald Burrill) wrote:


>                 You have not stated how many subjects (Ss) receive each 
> drug/dose combination.  If all 20 Ss receive all 4 combinations, as 
> implied by your assertion of 80 data points (below), then the design is 
> not completely given:  you must also have a factor representing the order 
> in which the combinations were encountered by each S.  If all Ss got the 
> various drug/dose combinations in the same order, you have no way of 
> telling whether (e.g.) the first combination affected responses to the 
> later combinations, nor even in which direction.  Also in this case, as 
> one other respondent pointed out, you have a repeated-measures design:
> that is, instead of  S(G x E)  as in the usual 2-way ANOVA (using S for 
> Subjects, G for druG, E for dosE), you have  S x G x E,  which implies 
> (inter alia) different error terms for G, E, and GE.
> 

Sorry, I assumed you would assume counterbalancing for order effects. 
You're right, a repeated measures design was assumed (but not stated).



> (In that notation, using R for the raw data values within each S, the two 
> designs above would be  R(S(B x E)  and  R(S) x G x E .  As remarked 
> below, the same ratios of mean squares are computed, whether R is 
> explicitly accounted for in the design or not.)
> 
> 
>         As others have pointed out, it makes no difference.  Your 
> hypotheses are tested by comparisons among the cell means, and the 
> denominator mean square for each hypothesis will be the estimated 
> sampling variance of the means in question.  Whether you use the mean of 
> 25 trials for each S, or the 25 raw trials themselves, you get the same 
> numbers. 
> 
>         As remarked above, this is not true.  One has the same numerical 
> estimates, and the same numbers of degrees of freedom in numerator and 
> denominator, for each hypothesis test.  As other respondents have 
> mentioned, if the raw data are a 0/1 dichotomy, there may be an advantage 
> in using a logistic rather than a normal model;  but if the proportions 
> (the several cell means) are not very close to 0 or 1, say between .25 
> and .75, there will not be much difference in the results of the 
> analysis. 



Many thanks to you and everyone else for your kind assistance. I think I
see the light now.

Jim

-- 
Remove SPAMBLOCK to reply


=================================================================
Instructions for joining and leaving this list and remarks about
the problem of INAPPROPRIATE MESSAGES are available at
                  http://jse.stat.ncsu.edu/
=================================================================

Reply via email to