Literature DB >> 24995866

Rare-variant association analysis: study designs and statistical tests.

Seunggeung Lee1, Gonçalo R Abecasis1, Michael Boehnke1, Xihong Lin2.   

Abstract

Despite the extensive discovery of trait- and disease-associated common variants, much of the genetic contribution to complex traits remains unexplained. Rare variants can explain additional disease risk or trait variability. An increasing number of studies are underway to identify trait- and disease-associated rare variants. In this review, we provide an overview of statistical issues in rare-variant association studies with a focus on study designs and statistical tests. We present the design and analysis pipeline of rare-variant studies and review cost-effective sequencing designs and genotyping platforms. We compare various gene- or region-based association tests, including burden tests, variance-component tests, and combined omnibus tests, in terms of their assumptions and performance. Also discussed are the related topics of meta-analysis, population-stratification adjustment, genotype imputation, follow-up studies, and heritability due to rare variants. We provide guidelines for analysis and discuss some of the challenges inherent in these studies and future research directions.
Copyright © 2014 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Mesh:

Year:  2014        PMID: 24995866      PMCID: PMC4085641          DOI: 10.1016/j.ajhg.2014.06.009

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


  140 in total

1.  Genomic control for association studies.

Authors:  B Devlin; K Roeder
Journal:  Biometrics       Date:  1999-12       Impact factor: 2.571

2.  Optimal tests for rare variant effects in sequencing association studies.

Authors:  Seunggeun Lee; Michael C Wu; Xihong Lin
Journal:  Biostatistics       Date:  2012-06-14       Impact factor: 5.899

3.  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

4.  SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples.

Authors:  Si Quang Le; Richard Durbin
Journal:  Genome Res       Date:  2010-10-27       Impact factor: 9.043

5.  Principal components analysis corrects for stratification in genome-wide association studies.

Authors:  Alkes L Price; Nick J Patterson; Robert M Plenge; Michael E Weinblatt; Nancy A Shadick; David Reich
Journal:  Nat Genet       Date:  2006-07-23       Impact factor: 38.330

6.  Power of deep, all-exon resequencing for discovery of human trait genes.

Authors:  Gregory V Kryukov; Alexander Shpunt; John A Stamatoyannopoulos; Shamil R Sunyaev
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-06       Impact factor: 11.205

7.  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

8.  A variational Bayes discrete mixture test for rare variant association.

Authors:  Benjamin A Logsdon; James Y Dai; Paul L Auer; Jill M Johnsen; Santhi K Ganesh; Nicholas L Smith; James G Wilson; Russell P Tracy; Leslie A Lange; Shuo Jiao; Stephen S Rich; Guillaume Lettre; Christopher S Carlson; Rebecca D Jackson; Christopher J O'Donnell; Mark M Wurfel; Deborah A Nickerson; Hua Tang; Alexander P Reiner; Charles Kooperberg
Journal:  Genet Epidemiol       Date:  2014-01       Impact factor: 2.135

9.  Detecting rare variant effects using extreme phenotype sampling in sequencing association studies.

Authors:  Ian J Barnett; Seunggeun Lee; Xihong Lin
Journal:  Genet Epidemiol       Date:  2012-11-26       Impact factor: 2.135

10.  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

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  405 in total

Review 1.  Genetics in bicuspid aortic valve disease: Where are we?

Authors:  Katia Bravo-Jaimes; Siddharth K Prakash
Journal:  Prog Cardiovasc Dis       Date:  2020-06-27       Impact factor: 8.194

Review 2.  The long tail and rare disease research: the impact of next-generation sequencing for rare Mendelian disorders.

Authors:  Tony Shen; Ariel Lee; Carol Shen; C Jimmy Lin
Journal:  Genet Res (Camb)       Date:  2015-09-14       Impact factor: 1.588

3.  An efficient resampling method for calibrating single and gene-based rare variant association analysis in case-control studies.

Authors:  Seunggeun Lee; Christian Fuchsberger; Sehee Kim; Laura Scott
Journal:  Biostatistics       Date:  2015-09-11       Impact factor: 5.899

4.  A general approach for combining diverse rare variant association tests provides improved robustness across a wider range of genetic architectures.

Authors:  Brian Greco; Allison Hainline; Jaron Arbet; Kelsey Grinde; Alejandra Benitez; Nathan Tintle
Journal:  Eur J Hum Genet       Date:  2015-10-28       Impact factor: 4.246

5.  The effect of phenotypic outliers and non-normality on rare-variant association testing.

Authors:  Paul L Auer; Alex P Reiner; Suzanne M Leal
Journal:  Eur J Hum Genet       Date:  2016-01-06       Impact factor: 4.246

Review 6.  Annual Research Review: Discovery science strategies in studies of the pathophysiology of child and adolescent psychiatric disorders--promises and limitations.

Authors:  Yihong Zhao; F Xavier Castellanos
Journal:  J Child Psychol Psychiatry       Date:  2016-01-06       Impact factor: 8.982

7.  Codon bias among synonymous rare variants is associated with Alzheimer's disease imaging biomarker.

Authors:  Jason E Miller; Manu K Shivakumar; Shannon L Risacher; Andrew J Saykin; Seunggeun Lee; Kwangsik Nho; Dokyoon Kim
Journal:  Pac Symp Biocomput       Date:  2018

8.  New Gene Variants Associated with the Risk of Chronic HBV Infection.

Authors:  Mengjie Fan; Jing Wang; Sa Wang; Tengyan Li; Hong Pan; Hankui Liu; Huifang Xu; Daria V Zhernakova; Stephen J O'Brien; Zhenru Feng; Le Chang; Erhei Dai; Jianhua Lu; Hongli Xi; Yanyan Yu; Jianguo Zhang; Binbin Wang; Zheng Zeng
Journal:  Virol Sin       Date:  2020-04-15       Impact factor: 4.327

9.  Statistical methods to detect novel genetic variants using publicly available GWAS summary data.

Authors:  Bin Guo; Baolin Wu
Journal:  Comput Biol Chem       Date:  2018-03-01       Impact factor: 2.877

10.  Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons.

Authors:  Alexandre Bolze; Bertrand Boisson; Barbara Bosch; Alexander Antipenko; Matthieu Bouaziz; Paul Sackstein; Malik Chaker-Margot; Vincent Barlogis; Tracy Briggs; Elena Colino; Aurora C Elmore; Alain Fischer; Ferah Genel; Angela Hewlett; Maher Jedidi; Jadranka Kelecic; Renate Krüger; Cheng-Lung Ku; Dinakantha Kumararatne; Alain Lefevre-Utile; Sam Loughlin; Nizar Mahlaoui; Susanne Markus; Juan-Miguel Garcia; Mathilde Nizon; Matias Oleastro; Malgorzata Pac; Capucine Picard; Andrew J Pollard; Carlos Rodriguez-Gallego; Caroline Thomas; Horst Von Bernuth; Austen Worth; Isabelle Meyts; Maurizio Risolino; Licia Selleri; Anne Puel; Sebastian Klinge; Laurent Abel; Jean-Laurent Casanova
Journal:  Proc Natl Acad Sci U S A       Date:  2018-08-02       Impact factor: 11.205

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