Evidence map›Paper›PMID 21789192›Full record

ArticlePloS one2011

Using an uncertainty-coding matrix in Bayesian regression models for haplotype-specific risk detection in family association studies.

Yung-Hsiang Huang, Mei-Hsien Lee, Wei J Chen, Chuhsing Kate Hsiao

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In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Yung-Hsiang HuangInstitute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan.
Mei-Hsien Lee
Wei J Chen
Chuhsing Kate Hsiao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Haplotype association studies based on family genotype data can provide more biological information than single marker association studies. Difficulties arise, however, in the inference of haplotype phase determination and in haplotype transmission/non-transmission status. Incorporation of the uncertainty associated with haplotype inference into regression models requires special care. This task can get even more complicated when the genetic region contains a large number of haplotypes. To avoid the curse of dimensionality, we employ a clustering algorithm based on the evolutionary relationship among haplotypes and retain for regression analysis only the ancestral core haplotypes identified by it. To integrate the three sources of variation, phase ambiguity, transmission status and ancestral uncertainty, we propose an uncertainty-coding matrix which combines these three types of variability simultaneously. Next we evaluate haplotype risk with the use of such a matrix in a Bayesian conditional logistic regression model. Simulation studies and one application, a schizophrenia multiplex family study, are presented and the results are compared with those from other family based analysis tools such as FBAT. Our proposed method (Bayesian regression using uncertainty-coding matrix, BRUCM) is shown to perform better and the implementation in R is freely available.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseModels, GeneticUncertaintyBayes TheoremComputer SimulationFamilyHaplotypesHumansLinkage DisequilibriumPolymorphism, Single NucleotideRegression AnalysisRisk FactorsSchizophreniaTaiwan

Identifiers

PMID21789192
PMCPMC3137600

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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.