Literature DB >> 19853241

The relationship between imputation error and statistical power in genetic association studies in diverse populations.

Lucy Huang1, Chaolong Wang, Noah A Rosenberg.   

Abstract

Genotype-imputation methods provide an essential technique for high-resolution genome-wide association (GWA) studies with millions of single-nucleotide polymorphisms. For optimal design and interpretation of imputation-based GWA studies, it is important to understand the connection between imputation error and power to detect associations at imputed markers. Here, using a 2x3 chi-square test, we describe a relationship between genotype-imputation error rates and the sample-size inflation required for achieving statistical power at an imputed marker equal to that obtained if genotypes at the marker were known with certainty. Surprisingly, typical imputation error rates (approximately 2%-6%) lead to a large increase in the required sample size (approximately 10%-60%), and in some African populations whose genotypes are particularly difficult to impute, the required sample-size increase is as high as approximately 30%-150%. In most populations, each 1% increase in imputation error leads to an increase of approximately 5%-13% in the sample size required for maintaining power. These results imply that in GWA sample-size calculations investigators will need to account for a potentially considerable loss of power from even low levels of imputation error and that development of additional genomic resources that decrease imputation error will translate into substantial reduction in the sample sizes needed for imputation-based detection of the variants that underlie complex human diseases.

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Year:  2009        PMID: 19853241      PMCID: PMC2775841          DOI: 10.1016/j.ajhg.2009.09.017

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


  27 in total

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2.  Testing untyped alleles (TUNA)-applications to genome-wide association studies.

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3.  A worldwide survey of haplotype variation and linkage disequilibrium in the human genome.

Authors:  Donald F Conrad; Mattias Jakobsson; Graham Coop; Xiaoquan Wen; Jeffrey D Wall; Noah A Rosenberg; Jonathan K Pritchard
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4.  A new multipoint method for genome-wide association studies by imputation of genotypes.

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Journal:  Nat Genet       Date:  2007-06-17       Impact factor: 38.330

5.  Methods to impute missing genotypes for population data.

Authors:  Zhaoxia Yu; Daniel J Schaid
Journal:  Hum Genet       Date:  2007-09-13       Impact factor: 4.132

Review 6.  Linkage disequilibrium in humans: models and data.

Authors:  J K Pritchard; M Przeworski
Journal:  Am J Hum Genet       Date:  2001-06-14       Impact factor: 11.025

7.  A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.

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Journal:  Science       Date:  2007-04-26       Impact factor: 47.728

8.  Imputation-based analysis of association studies: candidate regions and quantitative traits.

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Journal:  PLoS Genet       Date:  2007-05-30       Impact factor: 5.917

9.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Authors: 
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10.  A flexible and accurate genotype imputation method for the next generation of genome-wide association studies.

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Journal:  PLoS Genet       Date:  2009-06-19       Impact factor: 5.917

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  42 in total

1.  Assessing the impact of non-differential genotyping errors on rare variant tests of association.

Authors:  Scott Powers; Shyam Gopalakrishnan; Nathan Tintle
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2.  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

3.  Genomics: In search of rare human variants.

Authors:  Rasmus Nielsen
Journal:  Nature       Date:  2010-10-28       Impact factor: 49.962

4.  Practical Consideration of Genotype Imputation: Sample Size, Window Size, Reference Choice, and Untyped Rate.

Authors:  Boshao Zhang; Degui Zhi; Kui Zhang; Guimin Gao; Nita N Limdi; Nianjun Liu
Journal:  Stat Interface       Date:  2011       Impact factor: 0.582

5.  Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.

Authors:  Mengmeng Du; Paul L Auer; Shuo Jiao; Jeffrey Haessler; David Altshuler; Eric Boerwinkle; Christopher S Carlson; Cara L Carty; Yii-Der Ida Chen; Keith Curtis; Nora Franceschini; Li Hsu; Rebecca Jackson; Leslie A Lange; Guillaume Lettre; Keri L Monda; Deborah A Nickerson; Alex P Reiner; Stephen S Rich; Stephanie A Rosse; Jerome I Rotter; Cristen J Willer; James G Wilson; Kari North; Charles Kooperberg; Nancy Heard-Costa; Ulrike Peters
Journal:  Hum Mol Genet       Date:  2014-07-15       Impact factor: 6.150

6.  A generic coalescent-based framework for the selection of a reference panel for imputation.

Authors:  Bogdan Paşaniuc; Ram Avinery; Tom Gur; Christine F Skibola; Paige M Bracci; Eran Halperin
Journal:  Genet Epidemiol       Date:  2010-12       Impact factor: 2.135

7.  PreCimp: Pre-collapsing imputation approach increases imputation accuracy of rare variants in terms of collapsed variables.

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Journal:  Genet Epidemiol       Date:  2016-11-10       Impact factor: 2.135

8.  Power Analysis for Genetic Association Test (PAGEANT) provides insights to challenges for rare variant association studies.

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Review 9.  Genome-wide association studies in diverse populations.

Authors:  Noah A Rosenberg; Lucy Huang; Ethan M Jewett; Zachary A Szpiech; Ivana Jankovic; Michael Boehnke
Journal:  Nat Rev Genet       Date:  2010-05       Impact factor: 53.242

10.  Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond.

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Journal:  Genet Epidemiol       Date:  2014-09       Impact factor: 2.135

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