SNPassoc (Q19177)

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SNPs-Based Whole Genome Association Studies
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    SNPassoc
    SNPs-Based Whole Genome Association Studies

      Statements

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      2.1-0
      14 December 2022
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      PACKAGES.rds
      9 July 2026
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      1.0-2
      29 September 2006
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      1.1-0
      10 November 2006
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      1.1-1
      19 November 2006
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      1.3-0
      30 November 2006
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      1.4-1
      18 January 2007
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      1.4-2
      21 January 2007
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      1.4-3
      22 January 2007
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      1.4-4
      20 March 2007
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      1.4-5
      21 March 2007
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      1.4-6
      23 March 2007
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      1.4-8
      29 May 2007
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      1.4-9
      16 October 2007
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      1.5-1
      27 March 2008
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      1.5-2
      22 April 2008
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      1.5-3
      5 May 2008
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      1.5-6
      6 February 2009
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      1.5-7
      4 March 2009
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      1.5-8
      9 March 2009
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      1.6-0
      18 July 2009
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      1.8-1
      22 November 2011
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      1.8-4
      3 September 2012
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      1.8-5
      17 December 2012
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      1.9-1
      8 November 2013
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      1.9-2.1
      19 August 2020
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      1.9-2
      23 April 2014
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      2.0-0
      7 September 2020
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      2.0-1
      13 October 2020
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      2.0-2
      11 November 2020
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      2.0-11
      3 December 2021
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      2.0-12
      20 August 2022
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      2.0-17
      4 October 2022
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      2.0-18
      15 November 2022
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      2.1-2
      28 October 2024
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      2.3.1
      13 April 2026
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      Victor Moreno
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      13 April 2026
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      Functions to perform most of the common analysis in genome association studies are implemented. These analyses include descriptive statistics and exploratory analysis of missing values, calculation of Hardy-Weinberg equilibrium, analysis of association based on generalized linear models (either for quantitative or binary traits), and analysis of multiple SNPs (haplotype and epistasis analysis). Permutation test and related tests (sum statistic and truncated product) are also implemented. Max-statistic and genetic risk-allele score exact distributions are also possible to be estimated. The methods are described in Gonzalez JR et al., 2007 <doi:10.1093/bioinformatics/btm025>. This version includes internal copies of functions from the archived 'haplo.stats' package to maintain functionality.
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      Identifiers