generate_seqdata_OR: Function to simulate data for one variant by given parameters

Description Usage Arguments Value

Description

Function to simulate data for one variant by given parameters

Usage

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generate_seqdata_OR(N, preval, ncase, ncont, mafco, OR, mdcase, sdcase, mdcont,
  sdcont, me, sde, nsnp)

Arguments

N

population size

preval

prevalence rate for the disease

ncase

the number of case

ncont

the number of controls

mafco

MAF for controls

OR

the odds ratio

mdcase

average read depth in cases (double) >0#' @param sddcase, standard deviation of read depth in cases (double) >0

mdcont

average read depth in controls (double) >0

sde

standard deviation of error rate (double) >0

nsnp

number of variant

Ncont

number of controls

sddcont

standard deviation of read depth in controls (double) >0#' @param me, average error rate, probability that sequence call is wrong (double) >0

Value

MM - conditional expected value E(Gij|Dij)

P -estimated genotype frequencies P(G=0), P(G=1), P(G=2)

G - true genotype from which sequence data generated


Struglab/RVS documentation built on May 9, 2019, 3:11 p.m.