Whole-Genome Scan, in a Complex Disease, Using 11,245 Single-Nucleotide Polymorphisms: Comparison with Microsatellites

Despite the theoretical evidence of the utility of single-nucleotide polymorphisms (SNPs) for linkage analysis, no whole-genome scans of a complex disease have yet been published to directly compare SNPs with microsatellites. Here, we describe a whole-genome screen of 157 families with multiple case...

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Veröffentlicht in:American journal of human genetics 2004-07, Vol.75 (1), p.54-64
Hauptverfasser: John, Sally, Shephard, Neil, Liu, Guoying, Zeggini, Eleftheria, Cao, Manqiu, Chen, Wenwei, Vasavda, Nisha, Mills, Tracy, Barton, Anne, Hinks, Anne, Eyre, Steve, Jones, Keith W., Ollier, William, Silman, Alan, Gibson, Neil, Worthington, Jane, Kennedy, Giulia C.
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Sprache:eng
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Zusammenfassung:Despite the theoretical evidence of the utility of single-nucleotide polymorphisms (SNPs) for linkage analysis, no whole-genome scans of a complex disease have yet been published to directly compare SNPs with microsatellites. Here, we describe a whole-genome screen of 157 families with multiple cases of rheumatoid arthritis (RA), performed using 11,245 genomewide SNPs. The results were compared with those from a 10-cM microsatellite scan in the same cohort. The SNP analysis detected HLA*DRB1, the major RA susceptibility locus ( P=.00004), with a linkage interval of 31 cM, compared with a 50-cM linkage interval detected by the microsatellite scan. In addition, four loci were detected at a nominal significance level ( P
ISSN:0002-9297
1537-6605
DOI:10.1086/422195