Literature DB >> 22128051

Effect of linkage disequilibrium on the identification of functional variants.

Alun Thomas1, Haley J Abel, Yanming Di, Laura L Faye, Jing Jin, Jin Liu, Zheyan Wu, Andrew D Paterson.   

Abstract

We summarize the contributions of Group 9 of Genetic Analysis Workshop 17. This group addressed the problems of linkage disequilibrium and other longer range forms of allelic association when evaluating the effects of genotypes on phenotypes. Issues raised by long-range associations, whether a result of selection, stratification, possible technical errors, or chance, were less expected but proved to be important. Most contributors focused on regression methods of various types to illustrate problematic issues or to develop adaptations for dealing with high-density genotype assays. Study design was also considered, as was graphical modeling. Although no method emerged as uniformly successful, most succeeded in reducing false-positive results either by considering clusters of loci within genes or by applying smoothing metrics that required results from adjacent loci to be similar. Two unexpected results that questioned our assumptions of what is required to model linkage disequilibrium were observed. The first was that correlations between loci separated by large genetic distances can greatly inflate single-locus test statistics, and, whether the result of selection, stratification, possible technical errors, or chance, these correlations seem overabundant. The second unexpected result was that applying principal components analysis to genome-wide genotype data can apparently control not only for population structure but also for linkage disequilibrium.
© 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 22128051      PMCID: PMC3248791          DOI: 10.1002/gepi.20660

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  10 in total

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3.  A map of human genome variation from population-scale sequencing.

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4.  Worldwide human relationships inferred from genome-wide patterns of variation.

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Journal:  Science       Date:  2008-02-22       Impact factor: 47.728

5.  Case-control association testing by graphical modeling for the Genetic Analysis Workshop 17 mini-exome sequence data.

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6.  Power of association tests in the presence of multiple causal variants.

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8.  Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates.

Authors:  Laura L Faye; Shelley B Bull
Journal:  BMC Proc       Date:  2011-11-29

9.  Principal components ancestry adjustment for Genetic Analysis Workshop 17 data.

Authors:  Jing Jin; Jane E Cerise; Sun Jung Kang; Eun Jung Yoon; Seungtai Yoon; Nancy R Mendell; Stephen J Finch
Journal:  BMC Proc       Date:  2011-11-29

10.  Gene-based Higher Criticism methods for large-scale exonic single-nucleotide polymorphism data.

Authors:  Shiquan He; Zheyang Wu
Journal:  BMC Proc       Date:  2011-11-29
  10 in total
  4 in total

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2.  Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis.

Authors:  Alexander F Wilson; Andreas Ziegler
Journal:  Genet Epidemiol       Date:  2011       Impact factor: 2.135

3.  Joint linkage and association mapping of complex traits in shrub willow (Salix purpurea L.).

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Journal:  Ann Bot       Date:  2019-10-29       Impact factor: 4.357

4.  Population-based analysis of ocular Chlamydia trachomatis in trachoma-endemic West African communities identifies genomic markers of disease severity.

Authors:  A R Last; H Pickering; C H Roberts; F Coll; J Phelan; S E Burr; E Cassama; M Nabicassa; H M B Seth-Smith; J Hadfield; L T Cutcliffe; I N Clarke; D C W Mabey; R L Bailey; T G Clark; N R Thomson; M J Holland
Journal:  Genome Med       Date:  2018-02-26       Impact factor: 11.117

  4 in total

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