ArticleGenetic epidemiology2009
Haplotype-based analysis: a summary of GAW16 Group 4 analysis.
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.
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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Who cites it
6 citing papers in PubMed.
- Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance.Blood cancer journal · 2024Article
- Gene-Based Genome-Wide Association Study Identified Genes for Agronomic Traits in Maize.Biology · 2022Article
- Benefits and limitations of genome-wide association studies.Nature reviews. Genetics · 2019Review
- Rule-based induction method for haplotype comparison and identification of candidate disease loci.Genome medicine · 2012Article
- Article
- Genome-wide association studies for discrete traits.Genetic epidemiology · 2009Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
In this summary article, we describe the contributions included in the haplotype-based analysis group (Group 4) at the Genetic Analysis Workshop 16, which was held in September 17-20, 2008. Our group applied a large number of haplotype-based methods in the context of genome-wide association studies. Two general approaches were applied: a two-stage approach that selected significant single-nucleotide polymorphisms (SNPs) in the first stage and then created haplotypes in the second stage and genome-wide analysis of smaller sets of SNPs selected by sliding windows or estimating haplotype blocks. Genome-wide haplotype analyses performed in these ways were feasible. The presence of the very strong chromosome 6 association in the North American Rheumatoid Arthritis Consortium data was detected by every method, and additional analyses attempted to control for this strong result to allow detection of additional haplotype associations.
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