Fit Age-Period-Cohort models and Lee-Carter models with effects modeled by natural splines.
apc.LCa( data, keep.models = FALSE, ... ) show.apc.LCa( x, dev.scale = TRUE, top = "Ad", ... )
data |
A data frame that must have columns |
keep.models |
Logical. Should the |
... |
Further parameters passed on to |
x |
The result from a call to |
dev.scale |
Should the vertical position of the boxes with the models be scales relative to the deviance between the Age-drift model and the extended Lee-Carter model? |
top |
The model presented at the top of the plot of boxes (together with any other model with larger deviance) when vertical position is scaled by deviances. Only "Ad", "AP", "AC", "APa" or "ACa" will make sense. |
The function apc.LCa
fits all 9 models (well, 10) available as
extension and sub-models of the APC-model and compares them by
returning deviance and residual df.
Bendix Carstensen, http://bendixcarstensen.com
library( Epi ) clear() # Danish lung cancer incidence in 5x5x5 Lexis triangles data( lungDK ) lc <- subset( lungDK, Ax>40 )[,c("Ax","Px","D","Y")] names( lc )[1:2] <- c("A","P") head( lc ) al <- apc.LCa( lc, npar=c(9,6,6,6,10), keep.models=TRUE, maxit=500, eps=10e-3 ) show.apc.LCa( al, dev=TRUE ) # Danish mortality data ## Not run: data( M.dk ) mdk <- subset( M.dk, sex==1 )[,c("A","P","D","Y")] head( mdk ) al <- apc.LCa( mdk, npar=c(15,15,20,6,6), maxit=50, eps=10e-3, quiet=FALSE, VC=FALSE ) show.apc.LCa( al, dev=FALSE ) show.apc.LCa( al, dev=TRUE ) show.apc.LCa( al, top="AP" ) # Fit a reasonable model to Danish mortality data and plot results mAPa <- LCa.fit( mdk, model="APa", npar=c(15,15,20,6,6), c.ref=1930, a.ref=70, quiet=FALSE, maxit=250 ) par( mfrow=c(1,3) ) plot( mAPa ) ## End(Not run)
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