Evidence map›Paper›PMID 26916671›Full record

ArticleBiometrics2016

A novel random effect model for GWAS meta-analysis and its application to trans-ethnic meta-analysis.

Jingchunzi Shi, Seunggeun Lee

Abstract read
In one paragraph

Article in Biometrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
–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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Genome-wide studies define new genetic mechanisms of IgA vasculitis.medRxiv : the preprint server for health sciences · 2024
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  12. Genotyping-by-sequencing of pear (Horticulture research · 2017
    Article
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

2 authors.

Jingchunzi ShiDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.. shijingc@umich.edu.
Seunggeun LeeDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.. leeshawn@umich.edu.

Funding

Statistical methods for rare variant effects in sequencing association studiesR00HL113164 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEE, SEUNGGEUN SHAWN · 2013 to 2015
$710k
NHLBI NIH HHS R00 HL113164
6 · The paper itself

Abstract

Meta-analysis of trans-ethnic genome-wide association studies (GWAS) has proven to be a practical and profitable approach for identifying loci that contribute to the risk of complex diseases. However, the expected genetic effect heterogeneity cannot easily be accommodated through existing fixed-effects and random-effects methods. In response, we propose a novel random effect model for trans-ethnic meta-analysis with flexible modeling of the expected genetic effect heterogeneity across diverse populations. Specifically, we adopt a modified random effect model from the kernel regression framework, in which genetic effect coefficients are random variables whose correlation structure reflects the genetic distances across ancestry groups. In addition, we use the adaptive variance component test to achieve robust power regardless of the degree of genetic effect heterogeneity. Simulation studies show that our proposed method has well-calibrated type I error rates at very stringent significance levels and can improve power over the traditional meta-analysis methods. We reanalyzed the published type 2 diabetes GWAS meta-analysis (Consortium et al., 2014) and successfully identified one additional SNP that clearly exhibits genetic effect heterogeneity across different ancestry groups. Furthermore, our proposed method provides scalable computing time for genome-wide datasets, in which an analysis of one million SNPs would require less than 3 hours.

Indexed as

Meta-Analysis as TopicModels, StatisticalComputer SimulationDiabetes Mellitus, Type 2EthnicityGenetic HeterogeneityGenome-Wide Association StudyHumansPolymorphism, Single NucleotideEffect-size heterogeneityGWASKernel regressionMeta-analysisRandom effect modelTrans-ethnic meta-analysis

Identifiers

PMID26916671
PMCPMC4996751

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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.