Evidence map›Paper›PMID 19996610›Full record

ArticleHuman heredity2010

Statistical tests of genetic association in the presence of gene-gene and gene-environment interactions.

Wei Pan

Abstract read
In one paragraph

Article in Human heredity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
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

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2 · The registry

The trial behind it

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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

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

1 author.

Wei PanDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minn. 55455-0392, USA. weip@biostat.umn.edu

Funding

New Machine Learning Tools for Biomedical DataR01GM081535 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2007 to 2014
$2.2M
Statistical Methods for Genomic and Proteomic DataR01HL065462 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI PAN, WEI · 2002 to 2012
$1.5M
NHLBI NIH HHS HL65462NHLBI NIH HHS R01 HL065462NIGMS NIH HHS GM081535NIGMS NIH HHS R01 GM081535
6 · The paper itself

Abstract

backgroundWhile its importance is well recognized, it remains challenging to test genetic association in the presence of gene-gene (or gene-environment) interactions. A major technical difficulty lies in the fact that a general model of gene-gene interactions calls for the use of often a large number of parameters, leading to possibly reduced statistical power. An emerging theme of some recent work is to reduce the number of such parameters through dimension reduction. Wang et al. [2009] proposed such an approach based on the partial least squares (PLS) for dimension reduction. They compared their method with several others using simulated data, establishing that their PLS test performed best. Unfortunately, Wang et al. did not include in their evaluations several powerful tests just recently discovered for analyzing multiple SNPs in a candidate gene or region.

methodsIn this paper, we first extend these tests to the current context to detect gene-gene interactions in the presence of nuisance parameters, then compare these tests with the PLS test using the simulated data of Wang et al. [2009].

resultsIt is confirmed that some other tests can be more powerful than the PLS test, though there is no uniform winner. Some interesting, albeit not new, observations are also made: some of the new tests are more robust to the large number of parameters in a model and may thus perform well; on the other hand, even for a purely epistatic genetic model, some of the tests applied to a logistic main-effects model without any interaction terms may be superior to that based on a full model that explicitly accounts for gene-gene interactions.

conclusionThe proposed statistical tests are potentially useful in practice.

Indexed as

EnvironmentEpistasis, GeneticGenetic Association StudiesGenetic Predisposition to DiseaseHumansModels, Genetic

Identifiers

PMID19996610
PMCPMC2826874

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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.