Evidence map›Paper›PMID 21838810›Full record

ArticleBiometrics2012

A composite likelihood approach to latent multivariate Gaussian modeling of SNP data with application to genetic association testing.

Fang Han, Wei Pan

Abstract read
In one paragraph

Article in Biometrics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Multivariate Bayesian variable selection for multi-trait genetic fine mapping.Journal of the Royal Statistical Society. Series C, Applied statistics · 2025
    Article
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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

2 authors.

Fang HanDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Wei Pan

Funding

Powerful Inference and Prediction for Genetic AssociationR01HL105397 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2011 to 2018
$2.9M
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
Gene-set pathway analysis of GWAS data for T2DM and related quantitative traitsR21DK089351 · NIDDK · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2010 to 2011
$394k
NHLBI NIH HHS HL105397NHLBI NIH HHS HL65462NHLBI NIH HHS R01 HL065462NHLBI NIH HHS R01 HL105397NIDDK NIH HHS R21 DK089351NIGMS NIH HHS GM081535NIGMS NIH HHS R01 GM081535
6 · The paper itself

Abstract

Many statistical tests have been proposed for case-control data to detect disease association with multiple single nucleotide polymorphisms (SNPs) in linkage disequilibrium. The main reason for the existence of so many tests is that each test aims to detect one or two aspects of many possible distributional differences between cases and controls, largely due to the lack of a general and yet simple model for discrete genotype data. Here we propose a latent variable model to represent SNP data: the observed SNP data are assumed to be obtained by discretizing a latent multivariate Gaussian variate. Because the latent variate is multivariate Gaussian, its distribution is completely characterized by its mean vector and covariance matrix, in contrast to much more complex forms of a general distribution for discrete multivariate SNP data. We propose a composite likelihood approach for parameter estimation. A direct application of this latent variable model is to association testing with multiple SNPs in a candidate gene or region. In contrast to many existing tests that aim to detect only one or two aspects of many possible distributional differences of discrete SNP data, we can exclusively focus on testing the mean and covariance parameters of the latent Gaussian distributions for cases and controls. Our simulation results demonstrate potential power gains of the proposed approach over some existing methods.

Indexed as

Models, GeneticBiometryComputer SimulationGenetic Association StudiesGenetic Predisposition to DiseaseHumansLikelihood FunctionsMultivariate AnalysisNormal DistributionPolymorphism, Single Nucleotide

Identifiers

PMID21838810
PMCPMC3218301

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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.