Hi @Mohnasre,
Yes, sometimes the automatic filtering on the Community is a bit hard, so your message may have been falsely tag as "spam".
Concerning your topic and DSD analysis, there are very few information to help you, and you particularly don't explain anything about the study context, objective of the study, and your experience with DoE.
Definitive Screening Designs are foremost screening designs (as the name suggests), but they are also able to detect strong interaction and quadratic effects. You can read more about their performance and their detection abilities (as well as the possibility to fit a full RSM model from them) here. The possibility to fit a full RSM model from your design depends on the number of runs (here 22, including the 4 extra runs for 8 factors), and the number of active main effects detected. From JMP Help documentation, if you have less than 4 significant main effects (from your 8 factors), you could fit a RSM model on your data.
Concerning the analysis, I would recommend starting with :
- Fit Definitive Screening platform, the default platform used for the analysis of DSD. A script to run this analysis is present in the data table when creating this design.
- Fit Two Level Screening platform, that can effectively detect main effects as well as interaction and quadratic effects.
There are more estimation methods available in the Fit Model platform to fit Least Squares models, as well as Generalized regression models (with JMP Pro) using Two Stage Forward selection or Pruned Forward selection estimation methods.
Compare the models found by these platforms and see where they agree and differ. If the models are different, verify that the regression models do respect regression assumptions (with residuals analysis) before comparing their performances in terms of explainative (with R2 and R2 adjusted metrics, to be maximised with the lowest difference between the two) and predictive (with RMSE metric, to be minimized) performances, as well as model complexity (with information criteria like AICc and BIC, to be minimized).
Depending on the number of main effects detected in the model and precision of the model, you'll be able to evaluate if you have sufficiently answered your objective through this DSD with a useful and relevant model, or if an augmentation phase may be required to fit a more complete and precise model.
Hope these few suggestions may help you. If you need more precise feedback and help, you can provide more information and context, and/or share your (anonimized) data table.
Best,
Victor GUILLER
"It is not unusual for a well-designed experiment to analyze itself" (Box, Hunter and Hunter)