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Haplotypes and haplotype‐tagging single‐nucleotide polymorphism: Presentation Group 8 of Genetic Analysis Workshop 14
Author(s) -
Beckmann Lars,
Ziegler Andreas,
Duggal Priya,
BaileyWilson Joan E.
Publication year - 2005
Publication title -
genetic epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.301
H-Index - 98
eISSN - 1098-2272
pISSN - 0741-0395
DOI - 10.1002/gepi.20111
Subject(s) - haplotype , linkage disequilibrium , single nucleotide polymorphism , genetics , tag snp , biology , haplotype estimation , locus (genetics) , genetic association , snp , allele , genotype , gene
Abstract Moderately dense maps of single‐nucleotide polymorphism (SNP) markers across the human genome for both the simulated data set and data from the Collaborative Study of the Genetics of Alcoholism were available at Genetic Analysis Workshop 14 for the first time. This allowed examination of various novel and existing methods for haplotype analyses. Three contributors applied Mantel statistics in different ways for both linkage and association analysis by using the shared length between two haplotypes at a marker locus as a measure of genetic similarity. The results indicate that haplotype‐sharing based on Mantel statistics can be a powerful approach and needs further methodological evaluation. Four contributors investigated haplotype‐tagging SNP (htSNP) selection procedures, two contributors examined the use of multilocus haplotypes compared to single loci in association tests, and two contributors compared the accuracy of various methods for reconstructing haplotypes and estimating haplotype frequencies for both pedigree data and data from unrelated individuals. For all three different tasks, software packages and procedures gave similar results in regions of high linkage disequilibrium (LD). However, they were not as consistent in regions of moderate to low LD. One coalescence‐based approach for estimating haplotype frequencies, coupled with a Markov chain Monte Carlo technique, outperformed the other haplotype frequency estimation methods in regions of low LD. In conclusion, regardless of the task, results were similar in chromosomal regions of high LD. However, based on the differing results observed here, methodological improvements are required for chromosomal regions of low to moderate LD. Genet. Epidemiol. 29(Suppl. 1):S71–S59, 2005. © 2005 Wiley‐Liss, Inc.