Pitfalls in homozygosity mapping

被引:61
作者
Miano, MG
Jacobson, SG
Carothers, A
Hanson, I
Teague, P
Lovell, J
Cideciyan, AV
Haider, N
Stone, EM
Sheffield, VC
Wright, AF
机构
[1] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Int Inst Genet & Biophys, I-80125 Naples, Italy
[3] Univ Penn, Scheie Eye Inst, Dept Ophthalmol, Philadelphia, PA 19104 USA
[4] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[5] Univ Iowa, Dept Ophthalmol, Iowa City, IA 52242 USA
[6] Univ Iowa, Howard Hughes Med Inst, Iowa City, IA 52242 USA
关键词
D O I
10.1016/S0002-9297(07)62966-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There is much interest in use of identity-by-descent (IBD) methods to map genes, both in Mendelian and in complex disorders. Homozygosity mapping provides a rapid means of mapping autosomal recessive genes in consanguineous families by identifying chromosomal regions that show homozygous IBD segments in pooled samples. In this report, we point out some potential pitfalls that arose during the course of homozygosity mapping of the enhanced S-cone syndrome gene, resulting from (1) unexpected allelic heterogeneity, so that the region containing the disease locus was missed as a result of pooling; (2) identification of a homozygous IBD region unrelated to the disease locus; and (3) the potential for inflation of LOD scores as a result of underestimation of the extent of inbreeding, which Broman and Weber suggest may be quite common.
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收藏
页码:1348 / 1351
页数:4
相关论文
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