ArticleGenetic epidemiology2009
Association mapping by generalized linear regression with density-based haplotype clustering.
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 3 papers.
What it found
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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.
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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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Who cites it
3 citing papers in PubMed.
- Gene genealogies for genetic association mapping, with application to Crohn's disease.Frontiers in genetics · 2013Article
- Using an uncertainty-coding matrix in Bayesian regression models for haplotype-specific risk detection in family association studies.PloS one · 2011Article
- A novel approach for haplotype-based association analysis using family data.BMC bioinformatics · 2010Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Haplotypes of closely linked single-nucleotide polymorphisms (SNPs) potentially offer greater power than individual SNPs to detect association between genetic variants and disease. We present a novel approach for association mapping in which density-based clustering of haplotypes reduces the dimensionality of the general linear model (GLM)-based score test of association implemented in the HaploStats software (Schaid et al. [2002] Am. J. Hum. Genet. 70:425-434). A flexible haplotype similarity score, a generalization of previously used measures, forms the basis, for grouping haplotypes of probable recent common ancestry. All haplotypes within a cluster are assigned the same regression coefficient within the GLM, and evidence for association is assessed with a score statistic. The approach is applicable to both binary and continuous trait data, and does not require prior phase information. Results of simulation studies demonstrated that clustering enhanced the power of the score test to detect association, under a variety of conditions, while preserving valid Type-I error. Improvement in performance was most dramatic in the presence of extreme haplotype diversity, while a slight improvement was observed even at low diversity. Our method also offers, for binary traits, a slight advantage in power over a similar approach based on an evolutionary model (Tzeng et al. [2006] Am. J. Hum. Genet. 78:231-242).
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Registered trials
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