McClintick J, Koller D L, Pankratz N, Kirkwood S C, Naughton B, Foroud T
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Genet Epidemiol. 2001;21 Suppl 1:S528-33. doi: 10.1002/gepi.2001.21.s1.s528.
A two-step process was used to find loci contributing to the qualitative disease phenotype in the Genetic Analysis Workshop (GAW) 12 simulated data. The first step used parametric linkage analysis with a limited number of dominant and recessive models to detect linkage to chromosomal regions. Subsequently, a subset of the simulated biallelic sequence polymorphisms was used for transmission/disequilibrium tests and to build haplotypes to fine map the disease-predisposing polymorphism(s). A haplotype, strongly associated with the disease phenotype whose proximal end was within 39 base pairs of the functional allele for simulated major gene 6, was identified in the isolated population.
在遗传分析研讨会(GAW)12模拟数据中,采用两步法来寻找导致定性疾病表型的基因座。第一步使用参数连锁分析,采用数量有限的显性和隐性模型来检测与染色体区域的连锁。随后,将模拟的双等位基因序列多态性的一个子集用于传递/不平衡检验,并构建单倍型以精细定位疾病易感多态性。在隔离人群中鉴定出一种与疾病表型强烈相关的单倍型,其近端位于模拟主基因6功能等位基因的39个碱基对内。