Hi Bianca,

I hope you’ve solved your problem with SPSS and R probit analysis, but if you 
haven’t, I have your solution:

Based on the output you’ve given, I see that your residual deviance is 
under-dispersed (that the ratio of residual deviance to residual deviance df 
does is less than 1). However, you’ve told R to treat your dispersion parameter 
as 1 (you did this by using the ‘family = binomial’ argument). Instead, if you 
use ‘family=quasibinomial’ you allow the dispersion parameter to be estimated. 
This changes how the variance, SE, etc are calculated. Modeling it this way is 
akin to the SPSS method, and thus produces nearly-identical results. You may 
still see very, very minor differences in chi square goodness of fit, and 95% 
CI of the doses/concentrations, etc. but this is due to differences in rounding 
under the hood of the software.


Hope this helps!

 
Edwin R. Burgess IV, Ph.D.



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