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Generate errors and missing values in a (simulated) genotype matrix.

Usage

MkGenoErrors(
  SGeno,
  CallRate = 0.99,
  SnpError = 5e-04,
  ErrorFV = function(E) c((E/2)^2, E - (E/2)^2, E/2),
  ErrorFM = NULL,
  Error.shape = 0.5,
  CallRate.shape = 1,
  WithLog = FALSE
)

Arguments

SGeno

matrix with genotype data in Sequoia's format: 1 row per individual, 1 column per SNP, and genotypes coded as 0/1/2.

CallRate

either a single number for the mean call rate (genotyping success), OR a vector with the call rate at each SNP, OR a named vector with the call rate for each individual. In the third case, ParMis is ignored, and individuals in the pedigree (as id or as parent) not included in this vector are presumed non-genotyped.

SnpError

either a single value which will be combined with ErrorFV, or a length 3 vector with probabilities (observed given actual) hom|other hom, het|hom, and hom|het; OR a vector or 3XnSnp matrix with the genotyping error rate(s) for each SNP.

ErrorFV

function taking the error rate (scalar) as argument and returning a length 3 vector with hom->other hom, hom->het, het->hom. May be an 'ErrFlavour', e.g. 'version2.9'.

ErrorFM

function taking the error rate (scalar) as argument and returning a 3x3 matrix with probabilities that actual genotype i (rows) is observed as genotype j (columns). See below for details. To use, set ErrorFV = NULL

Error.shape

first shape parameter (alpha) of beta-distribution of per-SNP error rates. A higher value results in a flatter distribution.

CallRate.shape

as Error.shape, for per-SNP call rates.

WithLog

Include dataframe in output with which datapoints have been edited, with columns id - SNP - actual (original, input) - observed (edited, output).

Value

The input genotype matrix, with some genotypes replaced, and some set to missing (-9). If WithLog=TRUE, a list with 3 elements: GenoM, Log, and Counts_actual (genotype counts in input, to allow double checking of simulated genotyping error rate).