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Human Molecular Genetics Advance Access published online on January 20, 2004

Human Molecular Genetics, doi:10.1093/hmg/ddh060
© 2004 by Oxford University Press
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©2004 Oxford University Press

Article

The impact of SNP density on fine-scale patterns of linkage disequilibrium

Xiayi Ke 1, Sarah Hunt 2, William Tapper 3, Robert Lawrence 1, George Stavrides 2, Jilur Ghori 2, Pamela Whittaker 2, Andrew Collins 3, Andrew P. Morris 1, David Bentley 2, Lon R. Cardon 1, and Panos Deloukas 4*

1 Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
2 Wellcome Trust Sanger Institute, Hinxton, UK
3 University of Southampton, Southampton, UK
4 Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, CB10 1SA, United Kingdom

* To whom correspondence should be addressed. E-mail: panos{at}sanger.ac.uk.


   Abstract

Linkage disequilibrium (LD) is a measure of the degree of association between alleles in a population. The detection of disease-causing variants by association with neighbouring single nucleotide polymorphisms (SNPs) depends on the existence of strong LD between them. Previous studies have indicated that the extent of LD is highly variable in different chromosome regions and different populations, demonstrating the importance of genome-wide accurate measurement of LD at high resolution throughout the human genome. A uniform feature of these studies has been the inability to detect LD in regions of low marker density. To investigate the dependence of LD patterns on marker selection we performed a high-resolution study in African-American, Asian and UK Caucasian populations. We selected over 5,000 SNPs with an average spacing of approximately 1 SNP per 2 kb after validating circa 12,000 SNPs derived from a dense SNP collection (1 SNP per 0.3 kb on average). Applications of different statistical methods of LD assessment highlight similar areas of high and low LD. However, at high resolution, features such as overall sequence coverage in LD blocks and block boundaries vary substantially with respect to marker density. Model-based linkage disequilibrium unit (LDU) maps appear robust to marker density and consistently influenced by marker allele frequency. The results suggest that very dense marker sets will be required to yield stable views of fine-scale LD in the human genome.


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