Genotyping arrays enable the direct measurement of an individuals genotype at thousands of markers. 'plinkQC' facilitates genotype quality control for genetic association studies as described by Anderson and colleagues (2010) <doi:10.1038/nprot.2010.116>. It makes 'PLINK' basic statistics (e.g. missing genotyping rates per individual, allele frequencies per genetic marker) and relationship functions accessible from 'R' and generates a per-individual and per-marker quality control report. Individuals and markers that fail the quality control can subsequently be removed to generate a new, clean dataset. Removal of individuals based on relationship status is optimised to retain as many individuals as possible in the study.
Version: | 0.3.4 |
Depends: | R (≥ 3.6.0) |
Imports: | methods, optparse, data.table (≥ 1.11.0), R.utils, ggplot2, ggforce, ggrepel, cowplot, UpSetR, dplyr, igraph (≥ 1.2.4), sys |
Suggests: | testthat, mockery, formatR, knitr, rmarkdown |
Published: | 2021-07-15 |
DOI: | 10.32614/CRAN.package.plinkQC |
Author: | Hannah Meyer [aut, cre] |
Maintainer: | Hannah Meyer <hannah.v.meyer at gmail.com> |
BugReports: | https://github.com/meyer-lab-cshl/plinkQC/issues |
License: | MIT + file LICENSE |
URL: | https://meyer-lab-cshl.github.io/plinkQC/ |
NeedsCompilation: | no |
SystemRequirements: | plink (1.9) |
Materials: | README NEWS |
CRAN checks: | plinkQC results |
Reference manual: | plinkQC.pdf |
Vignettes: |
AncestryCheck 1000Genomes HapMap GenotypeQC_with_plinkQC |
Package source: | plinkQC_0.3.4.tar.gz |
Windows binaries: | r-devel: plinkQC_0.3.4.zip, r-release: plinkQC_0.3.4.zip, r-oldrel: plinkQC_0.3.4.zip |
macOS binaries: | r-release (arm64): plinkQC_0.3.4.tgz, r-oldrel (arm64): plinkQC_0.3.4.tgz, r-release (x86_64): plinkQC_0.3.4.tgz, r-oldrel (x86_64): plinkQC_0.3.4.tgz |
Old sources: | plinkQC archive |
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