IFP (version 0.2.4)

iter.mcmc: mcmc inference of causal models with all possible causal factors: G, G*G, G*E and E

Description

provides proportions of each causal factor of G, G*G, G*E and E based on relative concordance data

Usage

iter.mcmc(ppt,aj=2,n.iter,n.chains,thinning=5,init.cut,darray,x,n,model,mcmcrg=0.01)

Arguments

ppt

population lifetime incidence

aj

a constant for the stage of data collection

n.iter

number of mcmc iterations

n.chains

number of mcmc chain

thinning

mcmc thinning parameter (default=5)

init.cut

mcmc data cut

darray

indicating the array positions of available data among 9 relative pairs: 1:mzt,2:parent-offspring,3:dzt,4:sibling,5:2-direct(grandparent-grandchild),6:3rd(uncle-niece),7:3-direct(great-grandparent-great-grandchild),8:4th (causin),9:4d(great-great-grandparent-great-great-grandchild)

x

number of disease concordance of relative pairs

n

total number of relative pairs

model

an array, size of 4 (1: E component; 2: G component; 3: G*E component; 4: G*G component), indicating the existance of the causal component: 0: excluded; 1: included.

mcmcrg

parameter of the data collection stage (default=0.01)

Value

a list of rejectionRate, result summary, Gelman-Rubin diagnostics (point est. & upper C.I.) for output variables: e[1]: proportion of environmental factor (E) g[2]: proportion of genetic factor (G) ge[3]: proportion of gene-environment interaction (G*E) gg[4]: proportion of gene interactions (G*G) gn[5]: number of recessive genes in G ppe[6]: population proportion of interacting environment in G*E ppg[7]: population proportion of interacting genetic factor in G*E fd[8]: frequency of dominant genes in G fdge[9]: frequency of dominant genes in G*E gnge[10]: number of recessive genes in G*E ppd[11]: population proportion of dominant genes in G*G ppr[12]: population proportion of recessive genes in G*G kd[13]: number of dominant genes in G*G kr[14]: number of recessive genes in G*G

References

L. Park, J. Kim, A novel approach for identifying causal models of complex disease from family data, Genetics, 2015 Apr; 199, 1007-1016.

Examples

# NOT RUN {
### PLI=0.01.
ppt<-0.01

### a simple causal model with G and E components

pg<-0.007  # the proportion of G component in total populations
pgg<-0  # the proportion of G*G component in total populations
pge<-0  # the proportion of G*E component in total populations
e<-1-(1-ppt)/(1-pg)   # the proportion of E component in total populations

fd<-0.001  # one dominant gene
tt<-3      # the number of recessive genes

temp<-sqrt(1-((1-pg)/(1-fd)^2)^(1/tt))
fr<-c(array(0,length(fd)),array(temp,tt))
fd<-c(fd,array(0,tt))

rp<-drgegggne(fd,fr,c(0,0),c(0,0),c(0,0),c(0,0),0,e)

sdata<-rp[,3]/(rp[,2]+rp[,3])
#sdata<-round(sdata*500)

darray<-c(1:2,4:6)  
  ## available data= MZT, P-O, sibs, grandparent-grandchild, avuncular pair
n<-array(1000,length(darray))
x<-array()
for(i in 1:length(darray)){
x[i]<-rbinom(1,n[i],sdata[darray[i]])
}
model<-c(1,1,0,0)

## remove # from the following lines to test examples.
#iter.mcmc(ppt,2,15,2,1,1,darray,x,n,model) # provide a running test
#iter.mcmc(ppt,2,2000,2,10,500,darray,x,n,model) # provide a proper result

# }