Hello,
I have been analyzing data for an experiment measuring growth of human cells with 3 factors: 2 of which are independent variables that were controlled for, and the 3rd variable being the donor that the human cells came from (of which there are two). I have an n = 8, and the design was a 2^3 factorial. However, I'm currently finding that there are 3 ways to approach analysis of the data with regard to the variable "Donor":
1. I can simply include it as a categorical 2 level factor, in which case it enters the model and also shows up in the prediction profiler. As it turns out, there are interactions between "Donor" and the other two factors, which are conclusions that can be easily visualized as well. However, having this in the prediction profiler isn't particularly helpful because donor variability is something I will always have to deal with - I can't just keep 'maximizing' by going back to that same donor over and over.
2. I can change the 'Design Role' to a blocking variable. However I notice that when I fit a model, it basically results in the same model, with the exception that "Donor" no longer shows up in the Prediction Profiler. This is nice because I can elucidate what the other 2 factors (which were actual, controllable independent variables that I'd like to manipulate) were contributing. I read in an earlier post that blocking variables also can only show up in main effects, but this is not true since I am able to still model interactions. At this moment, I consider this the best approach.
3. Given that the 2 donors I chose are a subset of the infinitely large population of people present and future, I would probably consider this blocking variable to actually be "Random" and not "Fixed". However, based on some reading it seems like you do need around 5+ levels of the blocking variable for the estimation of variance to be accurate. As such, given that my dataset is small (n = 8, only 2 levels of the blocking variable), this may not be ideal.
Is my thinking on the right path?