Evidence map›Paper›PMID 20636464›Full record

ArticleAnnals of human genetics2010

Identification of interacting genes in genome-wide association studies using a model-based two-stage approach.

Zhaogong Zhang, Adan Niu, Qiuying Sha

Abstract read
In one paragraph

Article in Annals of human genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Zhaogong ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, MI 49931, USA.
Adan Niu
Qiuying Sha

Funding

Statistical Methods for Mapping Complex Disease GenesR01GM069940 · NIGMS · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI ZHANG, SHUANGLIN · 2005 to 2007
$682k
NIGMS NIH HHS R01 GM069940
6 · The paper itself

Abstract

In this paper, we propose a two-stage approach based on 17 biologically plausible models to search for two-locus combinations that have significant joint effects on the disease status in genome-wide association (GWA) studies. In the two-stage analyses, we only test two-locus joint effects of SNPs that show modest marginal effects. We use simulation studies to compare the power of our two-stage analysis with a single-marker analysis and a two-stage analysis by using a full model. We find that for most plausible interaction effects, our two-stage analysis can dramatically increase the power to identify two-locus joint effects compared to a single-marker analysis and a two-stage analysis based on the full model. We also compare two-stage methods with one-stage methods. Our simulation results indicate that two-stage methods are more powerful than one-stage methods. We applied our two-stage approach to a GWA study for identifying genetic factors that might be relevant in the pathogenesis of sporadic Amyotrophic Lateral Sclerosis (ALS). Our proposed two-stage approach found that two SNPs have significant joint effect on sporadic ALS while the single-marker analysis and the two-stage analysis based on the full model did not find any significant results.

Indexed as

Genome-Wide Association StudyModels, GeneticPolymorphism, Single NucleotideAmyotrophic Lateral SclerosisGenetic Predisposition to DiseaseHumans

Identifiers

PMID20636464
PMCPMC2923239

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Registered trials

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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.