OBJECTIVE: In isolated populations, 'background' linkage disequilibrium (LD) has been shown to extend over large genetic distances. This and their reduced environmental and genetic heterogeneity has stimulated interest in their potential for association mapping. We compared LD unit map distances with pair-wise measurements of LD in a dense single nucleotide polymorphism (SNP) set. METHODS: We genotyped 771 SNPs in an 8 Mb segment of chromosome 22 on 101 individuals from the isolated village of Talana, Sardinia, and compared with outbred European populations. RESULTS: Heterozygosity was remarkably similar in both populations. In contrast, the extent of LD observed was quite different. The decay of LD with distance is slower in the isolate. The differences in LD map lengths suggest that useful LD extends up to three times farther in the Sardinian population; smaller differences are seen with pairwise LD metrics. While LD map length slightly decreases with average relatedness, cryptic relatedness does not explain the decrease in LD map length. Haplotypes, block boundaries, and patterns of LD are similar in both populations, suggesting a shared distribution of recombination hotspots. CONCLUSIONS: About 15% fewer haplotype tagging SNPs need to be genotyped in the isolate, and possibly 70% fewer if selecting SNPs evenly spaced on the metric LD map. Copyright 2008 S. Karger AG, Basel.
OBJECTIVE: In isolated populations, 'background' linkage disequilibrium (LD) has been shown to extend over large genetic distances. This and their reduced environmental and genetic heterogeneity has stimulated interest in their potential for association mapping. We compared LD unit map distances with pair-wise measurements of LD in a dense single nucleotide polymorphism (SNP) set. METHODS: We genotyped 771 SNPs in an 8 Mb segment of chromosome 22 on 101 individuals from the isolated village of Talana, Sardinia, and compared with outbred European populations. RESULTS: Heterozygosity was remarkably similar in both populations. In contrast, the extent of LD observed was quite different. The decay of LD with distance is slower in the isolate. The differences in LD map lengths suggest that useful LD extends up to three times farther in the Sardinian population; smaller differences are seen with pairwise LD metrics. While LD map length slightly decreases with average relatedness, cryptic relatedness does not explain the decrease in LD map length. Haplotypes, block boundaries, and patterns of LD are similar in both populations, suggesting a shared distribution of recombination hotspots. CONCLUSIONS: About 15% fewer haplotype tagging SNPs need to be genotyped in the isolate, and possibly 70% fewer if selecting SNPs evenly spaced on the metric LD map. Copyright 2008 S. Karger AG, Basel.
Authors: Krishna R Veeramah; Anke Tönjes; Peter Kovacs; Arnd Gross; Daniel Wegmann; Patrick Geary; Daniela Gasperikova; Iwar Klimes; Markus Scholz; John Novembre; Michael Stumvoll Journal: Eur J Hum Genet Date: 2011-05-11 Impact factor: 4.246
Authors: Arnd Gross; Anke Tönjes; Peter Kovacs; Krishna R Veeramah; Peter Ahnert; Nab R Roshyara; Christian Gieger; Ina-Maria Rueckert; Markus Loeffler; Mark Stoneking; Heinz-Erich Wichmann; John Novembre; Michael Stumvoll; Markus Scholz Journal: BMC Genet Date: 2011-07-28 Impact factor: 2.797
Authors: Metten Somers; Loes M Olde Loohuis; Maartje F Aukes; Bogdan Pasaniuc; Kees C L de Visser; René S Kahn; Iris E Sommer; Roel A Ophoff Journal: Genes (Basel) Date: 2017-05-04 Impact factor: 4.096