plinkQC (version 0.2.2)

check_hwe: Identification of SNPs showing a significant deviation from Hardy-Weinberg- equilibrium (HWE)

Description

Runs and evaluates results from plink --hardy. It calculates the observed and expected heterozygote frequencies for all variants in the individuals that passed the perIndividualQC and computes the deviation of the frequencies from Hardy-Weinberg equilibrium (HWE) by HWE exact test. The p-values of the HWE exact test are displayed as histograms (stratified by all and low p-values), where the hweTh is used to depict the quality control cut-off for SNPs.

Usage

check_hwe(indir, name, qcdir = indir, hweTh = 1e-05,
  interactive = FALSE, path2plink = NULL, verbose = FALSE,
  showPlinkOutput = TRUE)

Arguments

indir

[character] /path/to/directory containing the basic PLINK data files name.bim, name.bed, name.fam files.

name

[character] Prefix of PLINK files, i.e. name.bed, name.bim, name.fam.

qcdir

[character] /path/to/directory where results will be written to. If perIndividualQC was conducted, this directory should be the same as qcdir specified in perIndividualQC, i.e. it contains name.fail.IDs with IIDs of individuals that failed QC. User needs writing permission to qcdir. Per default, qcdir=indir.

hweTh

[double] Significance threshold for deviation from HWE.

interactive

[logical] Should plots be shown interactively? When choosing this option, make sure you have X-forwarding/graphical interface available for interactive plotting. Alternatively, set interactive=FALSE and save the returned plot object (p_hwe) via ggplot2::ggsave(p=p_hwe, other_arguments) or pdf(outfile) print(p_hwe) dev.off().

path2plink

[character] Absolute path to PLINK executable (https://www.cog-genomics.org/plink/1.9/) i.e. plink should be accesible as path2plink -h. The full name of the executable should be specified: for windows OS, this means path/plink.exe, for unix platforms this is path/plink. If not provided, assumed that PATH set-up works and PLINK will be found by exec_wait('plink').

verbose

[logical] If TRUE, progress info is printed to standard out and specifically, if TRUE, plink log will be displayed.

showPlinkOutput

[logical] If TRUE, plink log and error messages are printed to standard out.

Value

Named list with i) fail_hwe containing a [data.frame] with CHR (Chromosome code), SNP (Variant identifier), TEST (Type of test: one of 'ALL', 'AFF', 'UNAFF', 'ALL(QT)', 'ALL(NP)'), A1 (Allele 1; usually minor), A2 (Allele 2; usually major), GENO ('/'-separated genotype counts: A1 hom, het, A2 hom), O(HET) (Observed heterozygote frequency E(HET) (Expected heterozygote frequency), P (Hardy-Weinberg equilibrium exact test p-value) for all SNPs that failed the hweTh and ii) p_hwe, a ggplot2-object 'containing' the HWE p-value distribution histogram which can be shown by (print(p_hwe)).

Details

check_hwe uses plink --remove name.fail.IDs --hardy to calculate the observed and expected heterozygote frequencies per SNP in the individuals that passed the perIndividualQC. It does so without generating a new dataset but simply removes the IDs when calculating the statistics.

For details on the output data.frame fail_hwe, check the original description on the PLINK output format page: https://www.cog-genomics.org/plink/1.9/formats#hwe.

Examples

# NOT RUN {
indir <- system.file("extdata", package="plinkQC")
qcdir <- tempdir()
name <- "data"
path2plink <- '/path/to/plink'
# the following code is not run on package build, as the path2plink on the
# user system is not known.
# }
# NOT RUN {
fail_hwe <- check_hwe(indir=indir, qcdir=qcdir, name=name, interactive=FALSE,
verbose=TRUE, path2plink=path2plink)
# }