plinkQC (Q123753)

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Genotype Quality Control with 'PLINK'
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    plinkQC
    Genotype Quality Control with 'PLINK'

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      0.3.4
      15 July 2021
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      PACKAGES.rds
      9 July 2026
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      0.1.0
      4 November 2018
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      0.1.1
      6 November 2018
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      0.2.0
      9 November 2018
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      0.2.1
      1 March 2019
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      0.2.2
      19 June 2019
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      0.2.3
      25 September 2019
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      0.3.0
      19 October 2019
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      0.3.2
      7 July 2020
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      0.3.3
      8 February 2021
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      1.0.0
      25 November 2025
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      1.0.1
      9 February 2026
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      1.1.0
      27 March 2026
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      27 March 2026
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      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. Additionally, there is a trained classifier to predict genomic ancestry of human samples.
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