Haplin (Q27112): Difference between revisions

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Property / Software Heritage ID: swh:1:snp:5cb755b2e60c9cf5b1dd5e4d7874130062894879 / rank
 
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Property / Software Heritage ID: swh:1:snp:5cb755b2e60c9cf5b1dd5e4d7874130062894879 / qualifier
 
Property / Software Heritage ID: swh:1:snp:5cb755b2e60c9cf5b1dd5e4d7874130062894879 / qualifier
 
point in time: 11 March 2024
Timestamp+2024-03-11T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Latest revision as of 17:02, 21 March 2024

Analyzing Case-Parent Triad and/or Case-Control Data with SNP Haplotypes
Language Label Description Also known as
English
Haplin
Analyzing Case-Parent Triad and/or Case-Control Data with SNP Haplotypes

    Statements

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    7.3.0
    20 May 2022
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    3.0.1
    27 May 2009
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    3.0.2
    10 January 2010
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    3.5
    26 May 2010
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    4.0
    27 January 2012
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    4.1
    16 March 2012
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    5.0.1
    8 March 2013
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    5.0.2
    18 March 2013
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    5.0
    6 February 2013
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    5.2
    2 May 2013
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    5.3
    23 May 2013
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    5.5
    15 May 2015
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    6.0.1
    26 May 2016
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    6.0
    25 May 2016
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    6.2.0
    28 February 2017
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    6.2.1
    18 October 2017
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    7.0.0
    28 May 2018
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    7.1.0
    17 April 2019
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    7.2.2
    7 January 2020
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    7.2.3
    7 September 2020
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    7.3.1
    8 February 2024
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    8 February 2024
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    Performs genetic association analyses of case-parent triad (trio) data with multiple markers. It can also incorporate complete or incomplete control triads, for instance independent control children. Estimation is based on haplotypes, for instance SNP haplotypes, even though phase is not known from the genetic data. 'Haplin' estimates relative risk (RR + conf.int.) and p-value associated with each haplotype. It uses maximum likelihood estimation to make optimal use of data from triads with missing genotypic data, for instance if some SNPs has not been typed for some individuals. 'Haplin' also allows estimation of effects of maternal haplotypes and parent-of-origin effects, particularly appropriate in perinatal epidemiology. 'Haplin' allows special models, like X-inactivation, to be fitted on the X-chromosome. A GxE analysis allows testing interactions between environment and all estimated genetic effects. The models were originally described in "Gjessing HK and Lie RT. Case-parent triads: Estimating single- and double-dose effects of fetal and maternal disease gene haplotypes. Annals of Human Genetics (2006) 70, pp. 382-396".
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