check_hwe: Identification of SNPs showing a significant deviation from...
In plinkQC: Genotype Quality Control with 'PLINK'

Description Usage Arguments Details Value Examples

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.

check_hwe(
  indir,
  name,
  qcdir = indir,
  hweTh = 1e-05,
  interactive = FALSE,
  path2plink = NULL,
  verbose = FALSE,
  showPlinkOutput = TRUE,
  keep_individuals = NULL,
  remove_individuals = NULL,
  exclude_markers = NULL,
  extract_markers = NULL,
  legend_text_size = 5,
  legend_title_size = 7,
  axis_text_size = 5,
  axis_title_size = 7,
  title_size = 9
)

`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 accessible 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`('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.
`keep_individuals`	[character] Path to file with individuals to be retained in the analysis. The file has to be a space/tab-delimited text file with family IDs in the first column and within-family IDs in the second column. All samples not listed in this file will be removed from the current analysis. See https://www.cog-genomics.org/plink/1.9/filter#indiv. Default: NULL, i.e. no filtering on individuals.
`remove_individuals`	[character] Path to file with individuals to be removed from the analysis. The file has to be a space/tab-delimited text file with family IDs in the first column and within-family IDs in the second column. All samples listed in this file will be removed from the current analysis. See https://www.cog-genomics.org/plink/1.9/filter#indiv. Default: NULL, i.e. no filtering on individuals.
`exclude_markers`	[character] Path to file with makers to be removed from the analysis. The file has to be a text file with a list of variant IDs (usually one per line, but it's okay for them to just be separated by spaces). All listed variants will be removed from the current analysis. See https://www.cog-genomics.org/plink/1.9/filter#snp. Default: NULL, i.e. no filtering on markers.
`extract_markers`	[character] Path to file with makers to be included in the analysis. The file has to be a text file with a list of variant IDs (usually one per line, but it's okay for them to just be separated by spaces). All unlisted variants will be removed from the current analysis. See https://www.cog-genomics.org/plink/1.9/filter#snp. Default: NULL, i.e. no filtering on markers.
`legend_text_size`	[integer] Size for legend text.
`legend_title_size`	[integer] Size for legend title.
`axis_text_size`	[integer] Size for axis text.
`axis_title_size`	[integer] Size for axis title.
`title_size`	[integer] Size for plot title.

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.

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)).

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: 
# run on all individuals and markers
fail_hwe <- check_hwe(indir=indir, qcdir=qcdir, name=name, interactive=FALSE,
verbose=TRUE, path2plink=path2plink)

# run on subset of individuals and markers
remove_individuals_file <- system.file("extdata", "remove_individuals",
package="plinkQC")
extract_markers_file <- system.file("extdata", "extract_markers",
package="plinkQC")
fail_hwe <- check_hwe(qcdir=qcdir, indir=indir,
name=name, interactive=FALSE, verbose=TRUE, path2plink=path2plink,
remove_individuals=remove_individuals_file,
extract_markers=extract_markers_file)

## End(Not run)