Evidence map›Paper›PMID 18770519›Full record

ArticleGenetic epidemiology2009

A joint association test for multiple SNPs in genetic case-control studies.

Tao Wang, Howard Jacob, Soumitra Ghosh, Xujing Wang, Zhao-Bang Zeng

Abstract read
In one paragraph

Article in Genetic epidemiology, 2009. 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

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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Advances in genome studies: The PAG 2010 conference.Functional & integrative genomics · 2010
    Article
  6. 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

5 authors.

Tao WangDivision of Biostatistics, Department of Population Health, Medical College of Wisconsin, Milwaukee, Wisconsin 53226-0509, USA. taowang@mcw.edu
Howard Jacob
Soumitra Ghosh
Xujing Wang
Zhao-Bang Zeng

Funding

Integrative genomics to to dissect the genetic regulation of T1D onsetR01DK080100 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, XUJING · 2007 to 2010
$1.0M
NIDDK NIH HHS R01 DK080100NIDDK NIH HHS R01DK080100
6 · The paper itself

Abstract

For a dense set of genetic markers such as single nucleotide polymorphisms (SNPs) on high linkage disequilibrium within a small candidate region, a haplotype-based approach for testing association between a disease phenotype and the set of markers is attractive in reducing the data complexity and increasing the statistical power. However, due to unknown status of the underlying disease variant, a comprehensive association test may require consideration of various combinations of the SNPs, which often leads to severe multiple testing problems. In this paper, we propose a latent variable approach to test for association of multiple tightly linked SNPs in case-control studies. First, we introduce a latent variable into the penetrance model to characterize a putative disease susceptible locus (DSL) that may consist of a marker allele, a haplotype from a subset of the markers, or an allele at a putative locus between the markers. Next, through using of a retrospective likelihood to adjust for the case-control sampling ascertainment and appropriately handle the Hardy-Weinberg equilibrium constraint, we develop an expectation-maximization (EM)-based algorithm to fit the penetrance model and estimate the joint haplotype frequencies of the DSL and markers simultaneously. With the latent variable to describe a flexible role of the DSL, the likelihood ratio statistic can then provide a joint association test for the set of markers without requiring an adjustment for testing of multiple haplotypes. Our simulation results also reveal that the latent variable approach may have improved power under certain scenarios comparing with classical haplotype association methods.

Indexed as

Polymorphism, Single NucleotideAlgorithmsAllelesCase-Control StudiesGene FrequencyGenetic MarkersGenetic Predisposition to DiseaseGenotypeHaplotypesHumansLikelihood FunctionsLinkage DisequilibriumLogistic ModelsModels, GeneticModels, StatisticalMolecular EpidemiologyGenetic Markers

Identifiers

PMID18770519
PMCPMC2719721

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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.