Estimating human inbreeding coefficients: Comparison of genealogical and marker heterozygosity approaches

被引:68
作者
Carothers, A. D. [1 ]
Rudan, I.
Kolcic, I.
Polasek, O.
Hayward, C.
Wright, A. F.
Campbell, H.
Teague, P.
Hastie, N. D.
Weber, J. L.
机构
[1] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, Sch Med, Dept Publ Hlth Sci, Edinburgh EH8 9AG, Midlothian, Scotland
[3] Univ Zagreb, Sch Med, Sch Publ Hlth Andrija Stampar, Zagreb 10000, Croatia
[4] Marshfield Med Res Fdn, Ctr Med Genet, Marshfield, WI 54449 USA
基金
英国医学研究理事会;
关键词
inbreeding; human isolates; marker heterozygosity; genealogy; Croatia;
D O I
10.1111/j.1469-1809.2006.00263.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have used genealogies and genomic polymorphisms to estimate individual inbreeding coefficients (F) in 50 subjects with an expected range (based on recent genealogies) of F from 0.0 to 0.0625. The estimates were based on two approaches, using genotypes respectively from 410 microsatellite markers (410-STR panel) and from 10,000 SNPs (10K-SNP panel). The latter was performed in a sub-sample of 15 individuals. We concluded that for both marker panels measures of inbreeding based on the excess of homozygosity over Hardy-Weinberg expectation were not closely correlated with 4-5 generation genealogical F-values. For the 10K-SNP panel we found two alternative measures which correlated more closely with F, based respectively on standard errors and on paired homozygosity of nearby SNPs over distances of 2-4 cM. We propose an empirical method for estimating standard errors and hence individual F-values, based on the variation between individual autosomes. This method could provide useful estimates of average F-values for groups of individuals in population-based studies of the effects of inbreeding/homozygosity on quantitative traits.
引用
收藏
页码:666 / 676
页数:11
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