Evidence map›Paper›PMID 19797904›Full record

ArticleHuman heredity2010

A unified framework for detecting genetic association with multiple SNPs in a candidate gene or region: contrasting genotype scores and LD patterns between cases and controls.

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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.

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3 · Its place in the literature

Who cites it

8 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, MMC 303, School of Public Health, University of Minnesota, Minneapolis, MN 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

It is critical to develop and apply powerful statistical tests for genetic association studies due to typically weak associations with complex human diseases or phenotypes. For population-based case-control studies with unphased multilocus genotype data, most of the existing methods are based on comparing genotype scores, e.g. allele frequencies, between the case and control groups. Another class of approaches are motivated to contrast linkage disequilibrium (LD) patterns between the two groups. It is expected that no single test can be uniformly most powerful across all situations, and different tests may perform better under different scenarios. A recent effort has been devoted to combining the above two classes of approaches, which however has some potential drawbacks. Here we propose a general and simple framework to unify the above two classes of approaches: it is based on the simple idea to incorporate LD measurements, in addition to genotype scores, as covariates in a logistic regression model, from which various tests can be constructed by taking advantage of the nice properties of the score statistics for the logistic model. It also has an advantage in easily accommodating covariates and other study designs. We use simulated data to show that our proposed tests performed well across several scenarios. In particular, in contrast to either of the two classes of the tests that is only powerful in detecting only one, but not both, of the two types of the distributional differences between cases and controls, our proposed tests are sensitive to both.

Indexed as

AlgorithmsLinkage DisequilibriumPolymorphism, Single NucleotideGenetic Association StudiesGenetic Predisposition to DiseaseGenome, HumanGenotypeHumansLogistic ModelsModels, Genetic

Identifiers

PMID19797904
PMCPMC2880731

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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.