Evidence map›Paper›PMID 26773050›Full record

ArticleGenetics2016

FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics.

Jianfei Huang, Kai Wang, Peng Wei, Xiangtao Liu, Xiaoming Liu, Kai Tan, Eric Boerwinkle, James B Potash, Shizhong Han

Abstract read
In one paragraph

Article in Genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 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

9 authors.

Jianfei HuangDepartment of Psychiatry, University of Iowa, Iowa City, Iowa 52242.
Kai WangDepartment of Biostatistics, University of Iowa, Iowa City, Iowa 52242.
Peng WeiDepartment of Biostatistics, University of Texas School of Public Health, Houston, Texas 77225.
Xiangtao LiuDepartment of Psychiatry, University of Iowa, Iowa City, Iowa 52242.
Xiaoming LiuHuman Genetics Center, University of Texas Health Science Center, Houston, Texas 77030.
Kai TanDepartment of Internal Medicine, University of Iowa, Iowa City, Iowa 52242 Interdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, Iowa 52242.
Eric BoerwinkleHuman Genetics Center, University of Texas Health Science Center, Houston, Texas 77030 Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030.
James B PotashDepartment of Psychiatry, University of Iowa, Iowa City, Iowa 52242.
Shizhong HanDepartment of Psychiatry, University of Iowa, Iowa City, Iowa 52242 Interdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, Iowa 52242 shizhong-han@uiowa.edu.

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
EPIGENETIC REGULATION OF STEM CELL FATE CHOICER01HG006130 · NHGRI · UNIVERSITY OF IOWA · PI TAN, KAI · 2012 to 2016
$1.7M
A SYSTEMS APPROACH TO THE GENETIC STUDY OF ALCOHOL DEPENDENCER01AA024486 · NIAAA · UNIVERSITY OF IOWA · PI HAN, SHIZHONG, TAN, KAI · 2017 to 2020
$1.6M
Fine mapping a gene sub-network underlying alcohol dependenceR01AA022994 · NIAAA · UNIVERSITY OF IOWA · PI HAN, SHIZHONG · 2014 to 2017
$1.3M
Computational Methods for Unraveling Combinatorial Gene RegulationR01GM108716 · NIGMS · UNIVERSITY OF IOWA · PI TAN, KAI · 2014 to 2017
$1.2M
A TOOLKIT FOR IDENTIFYING CAUSAL VARIANTS IN TRANSCRIPTIONAL ENHANCERSR01GM104369 · NIGMS · UNIVERSITY OF IOWA · PI TAN, KAI · 2014 to 2017
$1.2M
NHGRI NIH HHS R01 HG006130NIAAA NIH HHS R01 AA022994NIAAA NIH HHS R01AA022994NIAAA NIH HHS R01 AA024486NIEHS NIH HHS P30 ES005605NIGMS NIH HHS R01 GM104369NIGMS NIH HHS R01 GM108716Wellcome TrustWellcome Trust 076113
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have been widely used for identifying common variants associated with complex diseases. Despite remarkable success in uncovering many risk variants and providing novel insights into disease biology, genetic variants identified to date fail to explain the vast majority of the heritability for most complex diseases. One explanation is that there are still a large number of common variants that remain to be discovered, but their effect sizes are generally too small to be detected individually. Accordingly, gene set analysis of GWAS, which examines a group of functionally related genes, has been proposed as a complementary approach to single-marker analysis. Here, we propose a FL: exible and A: daptive test for G: ene S: ets (FLAGS), using summary statistics. Extensive simulations showed that this method has an appropriate type I error rate and outperforms existing methods with increased power. As a proof of principle, through real data analyses of Crohn's disease GWAS data and bipolar disorder GWAS meta-analysis results, we demonstrated the superior performance of FLAGS over several state-of-the-art association tests for gene sets. Our method allows for the more powerful application of gene set analysis to complex diseases, which will have broad use given that GWAS summary results are increasingly publicly available.

Indexed as

Models, GeneticModels, StatisticalComputer SimulationCrohn DiseaseGenome-Wide Association StudyGenotypeHumansPhenotypePolymorphism, Single Nucleotideassociationcomplex diseasegene setGWASsummary statistics

Identifiers

PMID26773050
PMCPMC4788129

What OpenQuestion holds

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Registered trials

None linked

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.