回复 第8楼 的 micro@:
I think what bothers you is the terminology of "bootstrap", and I guess I should NOT ambiguously use this word before statisticians who have a strict and dogmatic definition of "bootstrap".[s:12][s:12][s:12]
Let's forget about this terminology for now, and focus on the procedure. For instance, in clinical research, suppose you have a model establihsed in adult, and now you want to extend this model to research in the paeditric population. In other words, you want to re-establish a model in Children, but Children has lots of limitations on experimental conditions. and your goal is to make sure that your study design in children can ensure you to get a reasonably good model.
Assume that the model in the adult can be adjusted to paeditric population, and we can get a TRUE model in paeditic. <<<<<<<<<<<< This is my big assumption and it is often TRUE based on the historic data and our thorough understanding of biological system.
Then we simulate this TRUE model in Children for many replicates under the proposed study design (say, 500-1000. I probably should NOT call this bootstrap). The possible variability can be introduced over replicates, so these replicates can represent trials.
Finally, we fit these replicates again in using MCMC method instead of maximum likelihood. We could use Winbugs here but set the prior to non-informative and let the current data drive the posterior distribution (we regard the MCMC iteration in posterior distribution as the parameters uncertainty), and obtain the descriptive statistics of model parameters from replicates, compare them to the "TRUE" model, and conclude the probability of successful estimation of model parameters under the proposed study design (as I described in the previous reply).
My contact info is yaming dot su at gmail dot com. We can discuss over the phone or email if you want.