Ravages (version 1.1.3)

SKAT.continuous: Multi group SKAT test using Liu et al. approximation

Description

Peforms SKAT on a continuous phenotype using Liu et al. approximation

Usage

SKAT.continuous(x, NullObject, genomic.region = x@snps$genomic.region,
                weights = (1 - x@snps$maf)**24, maf.threshold = 0.5,
                estimation.pvalue = "kurtosis", cores = 10, debug = FALSE )

Value

A data frame containing for each genomic region:

stat

The observed statistics

p.value

The p-value of the test

If debug = TRUE, the mean, standard deviation, skewness and kurtosis used to compute the p-value are returned

Arguments

x

A bed.matrix

NullObject

A list returned from NullObject.parameters

genomic.region

A factor defining the genomic region of each variant

weights

A vector with the weight of each variant. By default, the weight of each variant is inversely proportionnal to its MAF, as it was computed in the original SKAT method

maf.threshold

The MAF above which variants are removed (default is to keep all variants)

estimation.pvalue

Whether to use the skewness ("skewness") or the kurtosis ("kurtosis") for the chi-square approximation

cores

How many cores to use for moments computation, set at 10 by default

debug

Whether to return the mean, standard deviation, skewness and kurtosis of the statistics. Set at FALSE by default

Details

The method from Liu et al. 2008 is used where p-values are estimated using a chi-square approximation from moment's

If estimation.pvalue = "kurtosis", the kurtosis is used instead of skewness in the chi-square approximation. This is equivalent to "liu.mod" in SKAT package.

References

Wu et al. 2011, Rare-variant association testing for sequencing data with the sequence kernel association test, American Journal of Human Genetics 82-93 doi:10.1016/j.ajhg.2011.05.029;

Liu et al. 2008, A new chi-square approximation to the distribution of non-negative definite quadratic forms in non-central normal variables, Computational Statistics & Data Analysis, doi:10.1016/j.csda.2008.11.025

See Also

NullObject.parameters, SKAT

Examples

# \donttest{
#Import data in a bed matrix
x <- as.bed.matrix(x=LCT.matrix.bed, fam=LCT.matrix.fam, bim=LCT.snps)
#Add population
x@ped[,c("pop", "superpop")] <- LCT.matrix.pop1000G[,c("population", "super.population")]

#Select EUR superpopulation
x <- select.inds(x, superpop=="EUR")
x@ped$pop <- droplevels(x@ped$pop)

#Group variants within known genes
x <- set.genomic.region(x)

#Filter of rare variants: only non-monomorphic variants with
#a MAF lower than 2.5%
#keeping only genomic regions with at least 10 SNPs
x1 <- filter.rare.variants(x, filter = "whole", maf.threshold = 0.025, min.nb.snps = 10)

#run SKAT using a random continuous phenotype
#Fit Null model
x1.H0 <- NullObject.parameters(rnorm(nrow(x1)), RVAT = "SKAT", pheno.type = "continuous")

SKAT.continuous(x1, x1.H0, cores = 1)
# }