ebGenotyping (version 2.0.1)

ecm: Genotyping and SNP Detection using Next Generation Sequencing Data

Description

This function implements the method described in 'An Empirical Bayes Method for Genotyping and SNP detection Using Multi-sample Next-generation Sequencing Data'.

Usage

ecm(dat,cvg,eps=1e-6,max.steps=500,eps.bisec=1e-6,ini.m=-7,ini.d=-7)

Arguments

dat

a n*m matrix: the ith row, jth column of the matrix represents the non-reference counts of ith sample at jth position.

cvg

a n*m matrix: the ith row, jth column of the matrix represents the depth of ith sample at jth position.

eps

a single value: a threshold to control the convergence criterion. The default is 1e-06.

max.steps

a single value: the maximum steps to run iterative algorithm to estimate parameters. The default is 500.(Adjustment is needed according to the number of parameters to estimate and the initial value of them.)

eps.bisec

a single value: a threshold to control the convergence criterion of bisection criterion. The default is 1e-06.

ini.m

the initial value of each element of mu. We suggest users to use default -7.

ini.d

the initial value of each element of delta. We suggest users to use default -7.

Value

par.est

a list including the estimate of position effect(mu), sample effect(delta), and the probability of RR and RV.

post.probs

3 matrix: the estimate of the posterior probabilities of 3 genotypes for n samples at m positions.

steps

the total steps to run iterative algorithm.

geno.est

a n*m matrix: the estimated genotypes(0 for RR, 1 for RV and 2 for VV) of n samples at m positions.

Details

This function implements the method described in 'An Empirical Bayes Method for Genotyping and SNP detection Using Multi-sample Next-generation Sequencing Data'. According to the paper, users can do genotyping with the estimated genotypes("geno.est"), and do SNP detection with the posterior probabilities of RR("post.probs$zRR"), based on the non-reference counts("dat")and depth("cvg").

References

Na You and Gongyi Huang.(2016) An Empirical Bayes Method for Genotyping and SNP detection Using Multi-sample Next-generation Sequencing Data.

Examples

#---------generate simulation data-----------
#start:generate simulation data#
set.seed(2016)
m <- 100
m0 <- m*0.95
m1 <- m-m0
n <- 30
Q <- 0.8
z <- cbind(matrix(0,n,m0),matrix(rbinom(n*m1,1,Q),n,m1))
b <- which(z==1)
R <- 0.8 # proportion of homozygous SNP
w <- rbinom(length(which(z==1)),1,R)
# z are genotypes
z[b[which(w==0)]] <- 1
z[b[which(w==1)]] <- 2
mu <- rep(-3,m)# stands for no effect
delta <- rep(-3,n)# stands for no effect
er.p <- -abs(outer(delta,mu,"+"))
p <- rlogit(er.p)
p[which(z==1)] <- 1/2
p[which(z==2)] <- 1-p[which(z==2)]
cvg <- matrix(rbinom(m*n,50,0.5),n,m)
dat <- matrix(sapply(1:(m*n),function(i) rbinom(1,cvg[i],p[i])),n,m)
#end:generate simulation data-#
#-----genotyping and SNP detection----------------
res <- ecm(dat=dat,cvg=cvg)
mean(z!=res$geno.est)#genotyping error
#----------call SNP---------
#start:call snp#
# define a function to calculate power, typeI error and FDR.
cutsnp <- function(fdr,alpha,true){
wh <- (true!=0)
tp <- sum((wh)&(fdr<alpha));
tn <- sum((!wh)&(fdr>=alpha));
fp <- sum((!wh)&(fdr<alpha));
fn <- sum((wh)&(fdr>=alpha));
pw  <- tp/(tp+fn);
t1 <- fp/(fp+tn);
fdr <- fp/(fp+tp);
return(c(TP=tp,TN=tn,FP=fp,FN=fn,power=pw,typeI=t1,FDR=fdr))
}
cutsnp(fdr=res$post.probs$zRR,alpha=0.001,true=z)
cutsnp(fdr=res$post.probs$zRR,alpha=0.01,true=z)
cutsnp(fdr=res$post.probs$zRR,alpha=0.05,true=z)
#end:call snp#