Evidence map›Paper›PMID 26087776›Full record

ArticleHuman heredity2015

A Generalized Sequential Bonferroni Procedure for GWAS in Admixed Populations Incorporating Admixture Mapping Information into Association Tests.

Wenan Chen, Chunfeng Ren, Huaizhen Qin, Kellie J Archer, Weiwei Ouyang, Nianjun Liu, Xiangning Chen, Xingguang Luo, Xiaofeng Zhu, Shumei Sun and 1 more

Abstract read
In one paragraph

Article in Human heredity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Wenan ChenDepartment of Biostatistics, Virginia Commonwealth University, Richmond, Va., USA.
Chunfeng Ren
Huaizhen Qin
Kellie J Archer
Weiwei Ouyang
Nianjun Liu
Xiangning Chen
Xingguang Luo
Xiaofeng Zhu
Shumei Sun
Guimin Gao

Funding

Center for Clinical and Translational ResearchUL1TR000058 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2012 to 2015
$12.5M
Multilevel Longitudinal Models and Causal Networks for Childhood ObesityU01HL101064 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SUN, SHUMEI S · 2009 to 2014
$1.8M
Genome Wide Haplotype Association AnalysisR01GM081488 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, NIANJUN · 2008 to 2012
$1.3M
Haplotyping and QTL Mapping in Pedigrees with Missing DataR01GM073766 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI GAO, GUIMIN · 2007 to 2011
$1.3M
Prolonged Juvenile State and Juvenile Protective Factors Affect Chronic DiseasesR01HD060913 · NICHD · VIRGINIA COMMONWEALTH UNIVERSITY · PI SUN, SHUMEI S · 2009 to 2011
$926k
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6 · The paper itself

Abstract

objectiveTo develop effective methods for GWAS in admixed populations such as African Americans.

methodsWe show that, when testing the null hypothesis that the test SNP is not in background linkage disequilibrium with the causal variants, several existing methods cannot control well the family-wise error rate (FWER) in the strong sense in GWAS. These existing methods include association tests adjusting for global ancestry and joint association tests that combine statistics from admixture mapping tests and association tests that correct for local ancestry. Furthermore, we describe a generalized sequential Bonferroni (smooth-GSB) procedure for GWAS that incorporates smoothed weights calculated from admixture mapping tests into association tests that correct for local ancestry. We have applied the smooth-GSB procedure to analyses of GWAS data on American Africans from the Atherosclerosis Risk in Communities (ARIC) Study.

resultsOur simulation studies indicate that the smooth-GSB procedure not only control the FWER, but also improves statistical power compared with association tests correcting for local ancestry.

conclusionThe smooth-GSB procedure can result in a better performance than several existing methods for GWAS in admixed populations.

Indexed as

Genome-Wide Association StudyModels, GeneticAtherosclerosisBlack or African AmericanChromosome MappingComputer SimulationHumansLinkage DisequilibriumPolymorphism, Single Nucleotide

Identifiers

PMID26087776
PMCPMC4821476

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.