Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2003 Oct;73(4):874-85.
doi: 10.1086/378590. Epub 2003 Sep 10.

Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs

Affiliations
Comparative Study

Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs

Jin P Szatkiewicz et al. Am J Hum Genet. 2003 Oct.

Erratum in

  • Am J Hum Genet. 2004 Nov;75(5):932

Abstract

Extreme discordant sibling pairs (EDSPs) are theoretically powerful for the mapping of quantitative-trait loci (QTLs) in humans. EDSPs have not been used much in practice, however, because of the need to screen very large populations to find enough pairs that are extreme and discordant. Given appropriate statistical methods, another alternative is to use moderately discordant sibling pairs (MDSPs)--pairs that are discordant but not at the far extremes of the distribution. Such pairs can be powerful yet far easier to collect than extreme discordant pairs. Recent work on statistical methods for QTL mapping in humans has included a number of methods that, though not developed specifically for discordant pairs, may well be powerful for MDSPs and possibly even EDSPs. In the present article, we survey the new statistics and discuss their applicability to discordant pairs. We then use simulation to study the type I error and the power of various statistics for EDSPs and for MDSPs. We conclude that the best statistic(s) for discordant pairs (moderate or extreme) is (are) to be found among the new statistics. We suggest that the new statistics are appropriate for many other designs as well-and that, in fact, they open the way for the exploration of entirely novel designs.

PubMed Disclaimer

Figures

Figure  1
Figure 1
Scatterplots of population, MDSP, and EDSP samples from models 1, 2, and 1′

Similar articles

Cited by

References

    1. Alcais A, Abel L (2000) Linkage analysis of quantitative trait loci: sib pairs or sibships? Hum Hered 50:251–256 - PubMed
    1. Amos CI (1994) Robust variance-components approach for assessing genetic linkage in pedigrees. Am J Hum Genet 54:535–543 - PMC - PubMed
    1. Blackwelder WC, Elston RC (1985) A comparison of sib-pair linkage tests for disease susceptibility loci. Genet Epidemiol 2:85–97 - PubMed
    1. Cai G, Li T, Deng H, Zhao J, Hu X, Murray RM, Liu X, Sham PC, Collier DA (2001) Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population. Am J Med Genet 105:321–327 - PubMed
    1. Davis S, Weeks DE (1997) Comparison of nonparametric statistics for detection of linkage in nuclear families: single-marker evaluation. Am J Hum Genet 61:1431–1444 - PMC - PubMed

Publication types

LinkOut - more resources