Literature DB >> 15114533

Graphical modeling of the joint distribution of alleles at associated loci.

Alun Thomas1, Nicola J Camp.   

Abstract

Pairwise linkage disequilibrium, haplotype blocks, and recombination hotspots provide only a partial description of the patterns of dependences and independences between the allelic states at proximal loci. On the gross scale, where recombination and spatial relationships dominate, the associations can be reasonably described in these terms. However, on the fine scale of current high-density maps, the mutation process is also important and creates associations between loci that are independent of the physical ordering and that can not be summarized with pairwise measures of association. Graphical modeling provides a standard statistical framework for characterizing precisely these sorts of complex stochastic data. Although graphical models are often used in situations in which assumptions lead naturally to specific models, it is less well known that estimation of graphical models is also a developed field. We show how decomposable graphical models can be fitted to dense genetic data. The objective function is the maximized log likelihood for the model penalized by a multiple of the model's degrees of freedom. We also describe how this can be modified to incorporate prior information of locus position. Simulated annealing is used to find good solutions. Part of the appeal of this approach is that categorical phenotypes can be included in the same analysis and association with polymorphisms can be assessed jointly with the interlocus associations. We illustrate our method with genotypic data from 25 loci in the ELAC2 gene. The results contain third- and fourth-order locus interactions and show that, at this density of markers, linkage disequilibrium is not a simple function of physical distance. Graphical models provide more flexibility to express these features of the joint distribution of alleles than do monotonic functions connecting physical and genetic maps.

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Year:  2004        PMID: 15114533      PMCID: PMC1182104          DOI: 10.1086/421249

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  16 in total

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Journal:  Am J Hum Genet       Date:  2001-11-26       Impact factor: 11.025

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Authors:  G C Johnson; L Esposito; B J Barratt; A N Smith; J Heward; G Di Genova; H Ueda; H J Cordell; I A Eaves; F Dudbridge; R C Twells; F Payne; W Hughes; S Nutland; H Stevens; P Carr; E Tuomilehto-Wolf; J Tuomilehto; S C Gough; D G Clayton; J A Todd
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

3.  High-resolution haplotype structure in the human genome.

Authors:  M J Daly; J D Rioux; S F Schaffner; T J Hudson; E S Lander
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

4.  A first-generation linkage disequilibrium map of human chromosome 22.

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Journal:  Nature       Date:  2002-07-10       Impact factor: 49.962

5.  Efficient selective screening of haplotype tag SNPs.

Authors:  Xiayi Ke; Lon R Cardon
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Journal:  Bioinformatics       Date:  2003-07-01       Impact factor: 6.937

7.  Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study.

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Journal:  Nat Genet       Date:  2001-02       Impact factor: 38.330

10.  Meta-analysis of associations of the Ser217Leu and Ala541Thr variants in ELAC2 (HPC2) and prostate cancer.

Authors:  Nicola J Camp; Sean V Tavtigian
Journal:  Am J Hum Genet       Date:  2002-12       Impact factor: 11.025

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  24 in total

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3.  Bayesian graphical models for genomewide association studies.

Authors:  Claudio J Verzilli; Nigel Stallard; John C Whittaker
Journal:  Am J Hum Genet       Date:  2006-05-30       Impact factor: 11.025

4.  Multilocus association mapping using variable-length Markov chains.

Authors:  Sharon R Browning
Journal:  Am J Hum Genet       Date:  2006-04-07       Impact factor: 11.025

5.  Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.

Authors:  A Thomas; N J Camp; J M Farnham; K Allen-Brady; L A Cannon-Albright
Journal:  Ann Hum Genet       Date:  2007-12-18       Impact factor: 1.670

6.  HaploBuild: an algorithm to construct non-contiguous associated haplotypes in family based genetic studies.

Authors:  Jason M Laramie; Jemma B Wilk; Anita L DeStefano; Richard H Myers
Journal:  Bioinformatics       Date:  2007-06-22       Impact factor: 6.937

7.  Estimation of haplotype associated with several quantitative phenotypes based on maximization of area under a receiver operating characteristic (ROC) curve.

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Journal:  J Hum Genet       Date:  2006-02-15       Impact factor: 3.172

8.  Multipoint approximations of identity-by-descent probabilities for accurate linkage analysis of distantly related individuals.

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Journal:  Am J Hum Genet       Date:  2008-03       Impact factor: 11.025

9.  A method and program for estimating graphical models for linkage disequilibrium that scale linearly with the number of loci, and their application to gene drop simulation.

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Journal:  Bioinformatics       Date:  2009-03-16       Impact factor: 6.937

10.  The conditional independences between variables derived from two independent identically distributed Markov random fields when pairwise order is ignored.

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Journal:  Math Med Biol       Date:  2009-11-25       Impact factor: 1.854

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