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PMID: 10762549 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Composite statistics for QTL mapping with moderately discordant sibling pairs.

American journal of human genetics ·Vol. 66 ·No. 5 ·2000-05-00 ·Pages 1642-60

Forrest WF, Feingold E

Abstract

Extreme discordant sibling-pair (EDSP) designs have been shown in theory to be very powerful for mapping quantitative-trait loci (QTLs) in humans. However, their practical applicability has been somewhat limited by the need to phenotype very large populations to find enough pairs that are extremely discordant. In this paper, we demonstrate that there is also substantial power in pairs that are only moderately discordant, and that designs using moderately discordant pairs can yield a more practical balance between phenotyping and genotyping efforts. The power we demonstrate for moderately discordant pairs stems from a new statistical result. Statistical analysis in discordant-pair studies is generally done by testing for reduced identity by descent (IBD) sharing in the pairs. By contrast, the most commonly-used statistical methods for more standard QTL mapping are Haseman-Elston regression and variance-components analysis. Both of these use statistics that are functions of the trait values given IBD information for the pedigree. We show that IBD sharing statistics and "trait value given IBD" statistics contribute complementary rather than redundant information, and thus that statistics of the two types can be combined to form more powerful tests of linkage. We propose a simple composite statistic, and test it with simulation studies. The simulation results show that our composite statistic increases power only minimally for extremely discordant pairs. However, it boosts the power of moderately discordant pairs substantially and makes them a very practical alternative. Our composite statistic is straightforward to calculate with existing software; we give a practical example of its use by applying it to a Genetic Analysis Workshop (GAW) data set.

MeSH Terms
Chromosome Mapping/methods,statistics & numerical data Computer Simulation Crosses, Genetic Female Gene Frequency/genetics Genotype Humans Likelihood Functions Lod Score Male Matched-Pair Analysis Models, Genetic Nuclear Family Quantitative Trait, Heritable Regression Analysis Research Design Sample Size Software
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Forrest W F
Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA. [email protected].
Feingold E
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
2000-05-00
Epub
2000-00-07
Pages
1642-60
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1378022
Subset
IM
Grants
NIGMS NIH HHS · GM31575 · United States
NIA NIH HHS · R01AG16989-01 · United States
NHGRI NIH HHS · R01HG00848 · United States
Corrections
ErratumIn
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