Sib-pair linkage analyses were used to search for linkage to a set of chromosome 19 and 21 marker loci in two sets of families with Alzheimer's disease. The advantage of this technique is that no assumption is made about the mode of inheritance of the disease. Some mild suggestions of linkage were f
Extensions to methods of sib-pair linkage analyses
β Scribed by W. Dana Flanders; Muin J. Khoury; G. P. Vogler
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 617 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
β¦ Synopsis
Sib-pair methods provide simple, robust, easily implemented ways to screen for linkage between a marker locus and a suspected disease susceptibility locus. The basic analysis reflects the idea that, in the presence of linkage, siblings who share more alleles at the marker locus should also tend to be concordant for disease. Available sib-pair methods do not lead directly to estimates of risk associated with nongenetic factors, may not account for a variable age-at-onset, or may require that the age-at-onset distribution be known. In this paper, we propose a method for sib-pair linkage analyses that allows for a variable age-at-onset using a logistic model, easily allows modelling of nongenetic factors, reflects the correlation of sibs within a sibship, and allows for nonzero risk in those without the susceptibility genotype. Based on a limited number of simulations, the method has as good or better power than another recently described method that also allows for a variable age-at-onset .
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The methods proposed by Haseman and Elston [1972] were used to estimate the proportion of genes identical by descent shared by each sib pair at each locus. These estimates were then used as a basis for obtaining all possible locus-locus correlations. The 12 significant correlations (P < .01) and the
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