This is the case study summary:
1 group,
0 individual covariates,
3 states (no antibodies, antibodies, dead),
4 events (not seen, no antibodies, antibodies, unknown)
1 age class
9 occasions
This is how the pattern matrices look like:
1. At occasion nº 4, all the individuals captured are in event "unknown" (no blood samples). I am setting the corresponding state assignment probabilities to zero, is that right?
2. In some cases, some parameter isn't estimable due to model structure and for that reason you can say E-SURGE to exclude them from the optimization process (it may help to reach convergence). For instance in my case, I have set this Umbrella Model:
{pi(t) phi(f.t) psi(f.t) beta(a(1)+a(2).[f.t]) delta(a(1).[f.t]+a(2).[f.t])}
In this multi-event context, which parameters are not estimable due to model structure? Given some previous trials and how parameters are confounded in simpler models (CJS for example), my guess is that (greek letters refer to above pattern matrices) these parameters are not estimable:
- final pi,
- final phi(s),
- final psi(s),
- final beta(s) (referred to a(2)),
- final delta(s) (referred to a(2)),
- first beta (referred to a(1)).
In particular, I would believe that final psi(s) and delta(s) are not estimable as a consequence of the final parameters over that they are conditional (respectively phi(s) and beta(s)) not to be estimable.
Even though, if I fix these parameters to one, E-SURGE doesn't get a result for that running.
What's wrong?
As these final parameters should be confounded parameters (their products are estimable but they are not each one for separate) , I thought that the value=1 for each of them might be generating some conflict and tried to fix the final parameter to the random value they were assigned by default (multiple random option).
Doing that, the model run but I am not sure at all if it is correct.
In fact, I get much more deviance with respect to the same model with no final parameters constrained.
For that reason I have tried to run a few times the same models with the same IVFV settings, i.e. (i) that model with those final parameters fixed to their random values, and (ii) that model with just the delta(s) at occasion 4 fixed to zero.
In case (i) I get several very different results in the parameters estimates (perhaps it is wrong to fix some of these final values) and in case (ii) I get a few very different results that I guess could be due to local minima (although the window about the saddle points didn't pop up).
3. Is there a suggested way to proceed in the model simplification? I mean in a normal CJS simplification I was told to modeling before the capture rate and after go on with modeling survival rate, is there some rule of thumb on this in the multi-event context?
4. Is there a way to run automatically the same models on a different dataset (but same nº of occasions, groups, age, states, events), or something similar ?
5. In the MS-DOS window during the running appears quite often a sentence saying "Ten first histories incompatibles with the model". Should I be worried about it?
Thanks for any help,
Simone