Donald,

Thank you for your detailed reply to my question. 

On 8 Jan 2000 22:22:57 -0800, [EMAIL PROTECTED] (Donald F.
Burrill) wrote:

>There are a limited number of patterns of four means in a 2x2 design that 
>can produce significant effects for all three formal sources of 
>variation.  One of those is  [a, a, a, b]  for some ordering of the four 
>cells, where  a  represents three means that are nearly equal and  b  is 
>a fourth mean that is different from the others.  This would be 
>consistend with your expectations as described above if B alone actually 
>has no effect on cell number but merely (?!) counteracts the toxic 
>effects of A, so that mean cell numbers for (0,0), (0,1), and (1,1) are 
>roughly equal, while average cell number for (1,0) is significantly 
>smaller than any of these due to the toxicity of treatment A.  
> This pattern will always produce two significant main effects and a 
>significant interaction if the average (a+b)/2 is significantly larger 
>than the average (a+a)/2 = a.

This is in fact what I see. I am using two drugs (A and B) in a
biological experiment comparing the number of cells in cultures under
different treatment models. My collaborator, for the past 10 years or
so, has been using drug/no drug (binary) levels. From a scientific and
a statistics viewpoint, I think multiple doses are better, especially
in cases where there are interactions.
 
>       If this is what you see, your post hoc analysis should compare 
>the mean of (1,0) with the average of the means of the other three cells 
>(the Scheffe' method would be preferable to the Tukey method).  

Thanks for this recommendation 

>You have not described your "post hoc" analysis.  For openers, which 
>"Tukey's test" did you use (there are at least three post hoc tests due, 
>or at any rate attributed, to Tukey)?  

I used Tukey's Honestly Significant Difference Test. I'll try
Scheffe's post hoc.

>Did you carry out a "complete" 
>post hoc analysis, accounting for 3 degrees of freedom all together, and 
>if so were the comparisons orthogonal?  
>For all you've said to the 
>contrary, you might equally well have done something as simple-minded as 
>examining all six possible pairwise contrasts -- that sort of thing 
>tends unfortunately to get programmed in packages because it's easy to 
>program, but it is not usually a useful way of detecting interesting 
>patterns among the means for designs with more than 3 cells.

After performing a basic GLM unianova that showed significance with
drug A, B, and A*B, I created another column that was numbered 0-3 for
the 4 different combinations of treatments: 0 = no A, no B; 1 = A, no
B; 2 = no A, B; 3 = A and B. Whether doing this represents a complete
post hoc analysis; I'm not sure.

A pseudo spreadsheet of the data (percentagewise just about the same
as my data) looks like this in SPSS

Drug A       Drug  B       Treatment    Set      Cell Number
    0               0                 0                1       100
    1               0                 1                 1      50
    0               1                 2                 1      102
    1               1                 3                 1       99
    0               0                 0                 2       98
    1               0                 1                 2       51
    0               1                 2                 2       101
    1               1                 3                 2       103
 
etc.

When I performed the primary unianova analysis, Drug A and Drug B were
the two independent variables, and Cell Number was the Dependent
variable. The post hoc comparison I used was to plug the Treatment
column (independent variable)  into a univariate anova analysis, and
compare treatment with cell number (dependent variable) using  Tukey's
HSD as a post hoc.  (Drug A and Drug B columns are not used when I
performed post hoc analysis. Set (experimental set) is also excluded
during analysis, and is just here for illustration.)

I know this is a relatively simple-minded approach, but it's the best
method I could come up with at the time. The  fundamental  question is
whether it is technically wrong to perform the analysis the way I did;
is this method I chose going to screw up my conclusions because the
analysis yields erroneous results ?

Hope to hear your thoughts on this one. Thanks for the help you've
already given, in any case!

-JE

>                                                               -- DFB.
> ------------------------------------------------------------------------
> Donald F. Burrill                                 [EMAIL PROTECTED]
> 348 Hyde Hall, Plymouth State College,          [EMAIL PROTECTED]
> MSC #29, Plymouth, NH 03264                                 603-535-2597
> 184 Nashua Road, Bedford, NH 03110                          603-471-7128  

Reply via email to