logisticRidgeGenotypesPredict: Predict fitted probabilities from genome-wide SNP data based...

In ridge: Ridge Regression with Automatic Selection of the Penalty Parameter

Predict fitted probabilities from genome-wide SNP data based on a file of coefficients

Description

Predict fitted probabilities from genome-wide SNP data based on a file of coefficients. Genotypes and fitted coefficients are provided as filenames, allowing the computation of fitted probabilities when SNP data are too large to be read into R.

Usage

logisticRidgeGenotypesPredict(genotypesfilename, betafilename,
phenotypesfilename = NULL, verbose = FALSE)

Arguments

genotypesfilename	character string: path to file containing SNP genotypes coded 0, 1, 2. See Input file formats.
betafilename	character string: path to file containing fitted coefficients. See Input file formats.
phenotypesfilename	(optional) character string: path to file in which to write out the fitted probabilities. See Output file formats. Whether or not this argument is supplied, the fitted coefficients are also returned by the function.
verbose	Logical: If TRUE, additional information is printed to the R outupt as the code runs. Defaults to FALSE.

Value

A vector of fitted probabilities, the same length as the number of individuals whose data are in genotypesfilename. If phenotypesfilename is supplied, the fitted probabilities are also written there.

Input file formats

genotypesfilename:

A header row, plus one row for each individual, one SNP per column. The header row contains SNP names. SNPs are coded as 0, 1, 2 for minor allele count. Missing values are not accommodated.

betafilename:

Two columns: First column is SNP names in same order as in genotypesfilename, second column is fitted coefficients. If the coefficients include an intercept then the first row of betafilename should contain it with the name Intercept in the first column. An Intercept thus labelled will be used appropriately in predicting the phenotypes. SNP names must match those in genotypesfilename. The format of betafilename is that of the output of linearRidgeGenotypes, meaning linearRidgeGenotypesPredict can be used to predict using coefficients fitted using linearRidgeGenotypes (see the example).

Output file format

Whether or not phenotypesfilename is provided, fitted probabilities are returned to the R workshpace. If phenotypesfilename is provided, fitted probabilities are written to the file specified (in addition).

phenotypesfilename:

One column, containing fitted probabilities, one individual per row.

Author(s)

Erika Cule

References

A semi-automatic method to guide the choice of ridge parameter in ridge regression. Cule, E. and De Iorio, M. (2012) arXiv:1205.0686v1 [stat.AP]

See Also

logisticRidgeGenotypes for model fitting. linearRidgeGenotypes and linearRidgeGenotypesPredict for corresponding functions to fit and predict on SNP data with continuous outcomes.

Examples

## Not run: 
genotypesfile <- system.file("extdata","GenBin_genotypes.txt",package = "ridge")
phenotypesfile <- system.file("extdata","GenBin_phenotypes.txt",package = "ridge")
betafile <- tempfile(pattern = "beta", fileext = ".dat")
beta_logisticRidgeGenotypes <- logisticRidgeGenotypes(genotypesfilename = genotypesfile,
                                                      phenotypesfilename = phenotypesfile,
                                                      betafilename = betafile)
pred_phen_geno <- logisticRidgeGenotypesPredict(genotypesfilename = genotypesfile,
                                                    betafilename = betafile)
## compare to output of logisticRidge
data(GenBin) ## Same data as in GenBin_genotypes.txt and GenBin_phenotypes.txt
beta_logisticRidge <- logisticRidge(Phenotypes ~ ., data = as.data.frame(GenBin))
pred_phen <- predict(beta_logisticRidge, type="response")
print(cbind(pred_phen_geno, pred_phen))
## Delete the temporary betafile
unlink(betafile)

## End(Not run)

ridge documentation built on April 11, 2022, 5:05 p.m.