Literature DB >> 18271029

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms.

Xiaoyi Gao1, Joshua Starmer, Eden R Martin.   

Abstract

Multiple testing is a challenging issue in genetic association studies using large numbers of single nucleotide polymorphism (SNP) markers, many of which exhibit linkage disequilibrium (LD). Failure to adjust for multiple testing appropriately may produce excessive false positives or overlook true positive signals. The Bonferroni method of adjusting for multiple comparisons is easy to compute, but is well known to be conservative in the presence of LD. On the other hand, permutation-based corrections can correctly account for LD among SNPs, but are computationally intensive. In this work, we propose a new multiple testing correction method for association studies using SNP markers. We show that it is simple, fast and more accurate than the recently developed methods and is comparable to permutation-based corrections using both simulated and real data. We also demonstrate how it might be used in whole-genome association studies to control type I error. The efficiency and accuracy of the proposed method make it an attractive choice for multiple testing adjustment when there is high intermarker LD in the SNP data set.

Mesh:

Year:  2008        PMID: 18271029     DOI: 10.1002/gepi.20310

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


  321 in total

1.  A family-based joint test for mean and variance heterogeneity for quantitative traits.

Authors:  Ying Cao; Taylor J Maxwell; Peng Wei
Journal:  Ann Hum Genet       Date:  2014-11-13       Impact factor: 1.670

2.  Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets.

Authors:  Miao-Xin Li; Juilian M Y Yeung; Stacey S Cherny; Pak C Sham
Journal:  Hum Genet       Date:  2011-12-06       Impact factor: 4.132

3.  Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy.

Authors:  Meredith A Bostrom; W H Linda Kao; Man Li; Hanna E Abboud; Sharon G Adler; Sudha K Iyengar; Paul L Kimmel; Robert L Hanson; Susanne B Nicholas; Rebekah S Rasooly; John R Sedor; Josef Coresh; Orly F Kohn; David J Leehey; Denyse Thornley-Brown; Erwin P Bottinger; Michael S Lipkowitz; Lucy A Meoni; Michael J Klag; Lingyi Lu; Pamela J Hicks; Carl D Langefeld; Rulan S Parekh; Donald W Bowden; Barry I Freedman
Journal:  Am J Kidney Dis       Date:  2011-11-25       Impact factor: 8.860

4.  Rapid and robust resampling-based multiple-testing correction with application in a genome-wide expression quantitative trait loci study.

Authors:  Xiang Zhang; Shunping Huang; Wei Sun; Wei Wang
Journal:  Genetics       Date:  2012-01-31       Impact factor: 4.562

5.  A large-scale candidate gene association study of age at menarche and age at natural menopause.

Authors:  Chunyan He; Peter Kraft; Daniel I Chasman; Julie E Buring; Constance Chen; Susan E Hankinson; Guillaume Paré; Stephen Chanock; Paul M Ridker; David J Hunter
Journal:  Hum Genet       Date:  2010-08-24       Impact factor: 4.132

6.  Powerful SNP-set analysis for case-control genome-wide association studies.

Authors:  Michael C Wu; Peter Kraft; Michael P Epstein; Deanne M Taylor; Stephen J Chanock; David J Hunter; Xihong Lin
Journal:  Am J Hum Genet       Date:  2010-06-11       Impact factor: 11.025

Review 7.  Statistical issues in longitudinal data analysis for treatment efficacy studies in the biomedical sciences.

Authors:  Chunyan Liu; Timothy P Cripe; Mi-Ok Kim
Journal:  Mol Ther       Date:  2010-06-29       Impact factor: 11.454

8.  Genetic variation in TRPS1 may regulate hip geometry as well as bone mineral density.

Authors:  Cheryl L Ackert-Bicknell; Serkalem Demissie; Shirng-Wern Tsaih; Wesley G Beamer; L Adrienne Cupples; Beverly J Paigen; Yi-Hsiang Hsu; Douglas P Kiel; David Karasik
Journal:  Bone       Date:  2012-01-28       Impact factor: 4.398

9.  An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between Variants.

Authors:  Joe R Davis; Laure Fresard; David A Knowles; Mauro Pala; Carlos D Bustamante; Alexis Battle; Stephen B Montgomery
Journal:  Am J Hum Genet       Date:  2015-12-31       Impact factor: 11.025

10.  Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci.

Authors:  Linda Kachuri; Christopher I Amos; James D McKay; Mattias Johansson; Paolo Vineis; H Bas Bueno-de-Mesquita; Marie-Christine Boutron-Ruault; Mikael Johansson; J Ramón Quirós; Sabina Sieri; Ruth C Travis; Elisabete Weiderpass; Loic Le Marchand; Brian E Henderson; Lynne Wilkens; Gary E Goodman; Chu Chen; Jennifer A Doherty; David C Christiani; Yongyue Wei; Li Su; Shelley Tworoger; Xuehong Zhang; Peter Kraft; David Zaridze; John K Field; Michael W Marcus; Michael P A Davies; Russell Hyde; Neil E Caporaso; Maria Teresa Landi; Gianluca Severi; Graham G Giles; Geoffrey Liu; John R McLaughlin; Yafang Li; Xiangjun Xiao; Gord Fehringer; Xuchen Zong; Robert E Denroche; Philip C Zuzarte; John D McPherson; Paul Brennan; Rayjean J Hung
Journal:  Carcinogenesis       Date:  2015-11-20       Impact factor: 4.944

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.