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#$Author: sinnwell $
#$Date: 2008/03/10 19:01:28 $
#$Header: /projects/genetics/cvs/cvsroot/haplo.stats/R/get.hapPair.q,v 1.1 2008/03/10 19:01:28 sinnwell Exp $
#$Locker: $
#$Log: get.hapPair.q,v $
#Revision 1.1 2008/03/10 19:01:28 sinnwell
#Initial revision
#
# get list for haplotype-pairs, or phased genotypes, under HWE
# return: 1) p.g: P(geno|hfreq, HWE)
# 2) x.haplo: design matrix for haplotype pairs (additive)
# 3) haplo.indx: index of hap pairs, referring to rows of haplo
get.hapPair <- function(haplo, haplo.freq, base.index) {
n.loci <- ncol(haplo)
n.haplo <- nrow(haplo)
haplo.indx <- expand.grid(1:n.haplo,1:n.haplo)
haplo.indx <- cbind(haplo.indx[,2],haplo.indx[,1])
haplo.indx <- haplo.indx[haplo.indx[,1] <= haplo.indx[,2],]
# Set up regression design matrices and beta coeff vectors
# Design matrix using base.index as baseline, and assuming
# haplotype effects are additive
haplo.reg <- (1:n.haplo)[-base.index]
x.haplo <- 1*outer(haplo.indx[,1], haplo.reg,"==") + 1*outer(haplo.indx[,2], haplo.reg,"==")
# Compute prior genotype probs (geno = pair of haplotypes)
p.g <- haplo.freq[haplo.indx[,1]] * haplo.freq[haplo.indx[,2]]
p.g <- p.g * ifelse(haplo.indx[,1] == haplo.indx[,2], 1, 2)
return(list(p.g=p.g, x.haplo=x.haplo, haplo.indx=haplo.indx))
}
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