Literature DB >> 23594497

Imputation of rare variants in next-generation association studies.

Jennifer L Asimit1, Eleftheria Zeggini.   

Abstract

The role of rare variants has become a focus in the search for association with complex traits. Imputation is a powerful and cost-efficient tool to access variants that have not been directly typed, but there are several challenges when imputing rare variants, most notably reference panel selection. Extensions to rare variant association tests to incorporate genotype uncertainty from imputation are discussed, as well as the use of imputed low-frequency and rare variants in the study of population isolates.
Copyright © 2013 S. Karger AG, Basel.

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Year:  2013        PMID: 23594497      PMCID: PMC3954458          DOI: 10.1159/000345602

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  51 in total

1.  Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes.

Authors:  Matthew Zawistowski; Shyam Gopalakrishnan; Jun Ding; Yun Li; Sara Grimm; Sebastian Zöllner
Journal:  Am J Hum Genet       Date:  2010-11-12       Impact factor: 11.025

2.  ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data.

Authors:  Jennifer L Asimit; Aaron G Day-Williams; Andrew P Morris; Eleftheria Zeggini
Journal:  Hum Hered       Date:  2012-03-22       Impact factor: 0.444

3.  ADAMTSL3 as a candidate gene for schizophrenia: gene sequencing and ultra-high density association analysis by imputation.

Authors:  David J Dow; Julie Huxley-Jones; Jamie M Hall; Clyde Francks; Peter R Maycox; James N C Kew; Israel S Gloger; Nalini A L Mehta; Fiona M Kelly; Pierandrea Muglia; Gerome Breen; Sarah Jugurnauth; Inti Pederoso; David St Clair; Dan Rujescu; Michael R Barnes
Journal:  Schizophr Res       Date:  2011-01-15       Impact factor: 4.939

4.  Detection of sharing by descent, long-range phasing and haplotype imputation.

Authors:  Augustine Kong; Gisli Masson; Michael L Frigge; Arnaldur Gylfason; Pasha Zusmanovich; Gudmar Thorleifsson; Pall I Olason; Andres Ingason; Stacy Steinberg; Thorunn Rafnar; Patrick Sulem; Magali Mouy; Frosti Jonsson; Unnur Thorsteinsdottir; Daniel F Gudbjartsson; Hreinn Stefansson; Kari Stefansson
Journal:  Nat Genet       Date:  2008-09       Impact factor: 38.330

5.  Genotype imputation with thousands of genomes.

Authors:  Bryan Howie; Jonathan Marchini; Matthew Stephens
Journal:  G3 (Bethesda)       Date:  2011-11-01       Impact factor: 3.154

6.  The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals.

Authors:  Martin Ladouceur; Zari Dastani; Yurii S Aulchenko; Celia M T Greenwood; J Brent Richards
Journal:  PLoS Genet       Date:  2012-02-02       Impact factor: 5.917

7.  Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis.

Authors:  Marine Germain; Noémie Saut; Tiphaine Oudot-Mellakh; Luc Letenneur; Anne-Marie Dupuy; Marion Bertrand; Marie-Christine Alessi; Jean-Charles Lambert; Diana Zelenika; Joseph Emmerich; Laurence Tiret; Francois Cambien; Mark Lathrop; Philippe Amouyel; Pierre-Emmanuel Morange; David-Alexandre Trégouët
Journal:  PLoS One       Date:  2012-06-04       Impact factor: 3.240

8.  Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.

Authors:  Manuel A Rivas; Mélissa Beaudoin; Agnes Gardet; Christine Stevens; Yashoda Sharma; Clarence K Zhang; Gabrielle Boucher; Stephan Ripke; David Ellinghaus; Noel Burtt; Tim Fennell; Andrew Kirby; Anna Latiano; Philippe Goyette; Todd Green; Jonas Halfvarson; Talin Haritunians; Joshua M Korn; Finny Kuruvilla; Caroline Lagacé; Benjamin Neale; Ken Sin Lo; Phil Schumm; Leif Törkvist; Marla C Dubinsky; Steven R Brant; Mark S Silverberg; Richard H Duerr; David Altshuler; Stacey Gabriel; Guillaume Lettre; Andre Franke; Mauro D'Amato; Dermot P B McGovern; Judy H Cho; John D Rioux; Ramnik J Xavier; Mark J Daly
Journal:  Nat Genet       Date:  2011-10-09       Impact factor: 38.330

9.  Discovery of rare variants via sequencing: implications for the design of complex trait association studies.

Authors:  Bingshan Li; Suzanne M Leal
Journal:  PLoS Genet       Date:  2009-05-15       Impact factor: 5.917

10.  An evaluation of statistical approaches to rare variant analysis in genetic association studies.

Authors:  Andrew P Morris; Eleftheria Zeggini
Journal:  Genet Epidemiol       Date:  2010-02       Impact factor: 2.135

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  4 in total

1.  Some surprising twists on the road to discovering the contribution of rare variants to complex diseases.

Authors:  Duncan C Thomas
Journal:  Hum Hered       Date:  2013-04-11       Impact factor: 0.444

2.  Accurate Imputation-Based Screening of Gln368Ter Myocilin Variant in Primary Open-Angle Glaucoma.

Authors:  Puya Gharahkhani; Kathryn P Burdon; Alex W Hewitt; Matthew H Law; Emmanuelle Souzeau; Grant W Montgomery; Graham Radford-Smith; David A Mackey; Jamie E Craig; Stuart MacGregor
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-08       Impact factor: 4.799

3.  Exploring Impact of Rare Variation in Systemic Lupus Erythematosus by a Genome Wide Imputation Approach.

Authors:  Manuel Martínez-Bueno; Marta E Alarcón-Riquelme
Journal:  Front Immunol       Date:  2019-02-26       Impact factor: 7.561

Review 4.  Two-phase and family-based designs for next-generation sequencing studies.

Authors:  Duncan C Thomas; Zhao Yang; Fan Yang
Journal:  Front Genet       Date:  2013-12-13       Impact factor: 4.599

  4 in total

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