A method for the genomic screening of quantitative traits using extreme discordant sib pairs (EDSPs) has recently been described by Risch and Zhang [1995;1996]. For many models relevant to common, genetically complex diseases, EDSPs are the most powerful siblings for detecting linkage. Thus, if such
Evaluation of screening strategies to detect an oligogenic disease
β Scribed by John J. Rogus; Dr. Jonathan L. Haines
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 276 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
β¦ Synopsis
Using data simulated to reflect an oligogenic disease, we evaluated screening strategies based on lod-score and weighted painvise correlation (WPC) analysis with respect to their ability to efficiently identify regions near disease loci. Lodscore analysis was done twice, once assuming a near-recessive mode of inheritance with a high penetrance and again assuming a semidominant mode of inheritance with lower penetrance. Under the near-recessive model, no disease loci were correctly identified, while there was one false positive result. Under the semidominant model, DlG31 was correctly identified, and there were two false positive results. Due to the lack of highly informative families and possible sensitivity to parameter misspecification, this poor performance was not unexpected. WPC, on the other hand, is assumption-free and thus potentially more powerful than a misspecified parametric model, but almost certainly less powerfid than a well-specified parametric model. Using WPC modified to handle binary phenotypes with no age-of-onset, we found results closely resembling those under the semidominant model, although no markers near disease loci exceeded the theoretical critical value for WPC.
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