Literature DB >> 12970846

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

Jin P Szatkiewicz1, Karen T Cuenco, Eleanor Feingold.   

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.

Entities:  

Mesh:

Year:  2003        PMID: 12970846      PMCID: PMC1180609          DOI: 10.1086/378590

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  33 in total

1.  Haseman and Elston revisited.

Authors:  R C Elston; S Buxbaum; K B Jacobs; J M Olson
Journal:  Genet Epidemiol       Date:  2000-07       Impact factor: 2.135

2.  Linkage analysis of quantitative trait loci: sib pairs or sibships?

Authors:  A Alcaïs; L Abel
Journal:  Hum Hered       Date:  2000 Jul-Aug       Impact factor: 0.444

3.  Variance-Components QTL linkage analysis of selected and non-normal samples: conditioning on trait values.

Authors:  P C Sham; J H Zhao; S S Cherny; J K Hewitt
Journal:  Genet Epidemiol       Date:  2000       Impact factor: 2.135

4.  Optimal sibship selection for genotyping in quantitative trait locus linkage analysis.

Authors:  S Purcell; S S Cherny; J K Hewitt; P C Sham
Journal:  Hum Hered       Date:  2001       Impact factor: 0.444

5.  Equivalence between Haseman-Elston and variance-components linkage analyses for sib pairs.

Authors:  P C Sham; S Purcell
Journal:  Am J Hum Genet       Date:  2001-05-14       Impact factor: 11.025

6.  Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticism.

Authors:  Jan Fullerton; Matthew Cubin; Hemant Tiwari; Chenxi Wang; Amarjit Bomhra; Stuart Davidson; Sue Miller; Christopher Fairburn; Guy Goodwin; Michael C Neale; Simon Fiddy; Richard Mott; David B Allison; Jonathan Flint
Journal:  Am J Hum Genet       Date:  2003-02-20       Impact factor: 11.025

7.  Mapping quantitative trait loci in oligogenic models.

Authors:  H K Tang; D Siegmund
Journal:  Biostatistics       Date:  2001-06       Impact factor: 5.899

8.  Regression-based quantitative-trait-locus mapping in the 21st century.

Authors:  Eleanor Feingold
Journal:  Am J Hum Genet       Date:  2002-08       Impact factor: 11.025

9.  The "possible triangle" test for extreme discordant sib pairs.

Authors:  R Kruse; S A Seuchter; M P Baur; M Knapp
Journal:  Genet Epidemiol       Date:  1997       Impact factor: 2.135

10.  Combining extremely concordant sibpairs with extremely discordant sibpairs provides a cost effective way to linkage analysis of quantitative trait loci.

Authors:  C Gu; A Todorov; D C Rao
Journal:  Genet Epidemiol       Date:  1996       Impact factor: 2.135

View more
  8 in total

1.  Theoretical and empirical power of regression and maximum-likelihood methods to map quantitative trait loci in general pedigrees.

Authors:  Xijiang Yu; Sara A Knott; Peter M Visscher
Journal:  Am J Hum Genet       Date:  2004-05-19       Impact factor: 11.025

2.  A powerful and robust new linkage statistic for discordant sibling pairs.

Authors:  Jin P Szatkiewicz; Eleanor Feingold
Journal:  Am J Hum Genet       Date:  2004-09-13       Impact factor: 11.025

3.  Robust score statistics for QTL linkage analysis.

Authors:  Samsiddhi Bhattacharjee; Chia-Ling Kuo; Nandita Mukhopadhyay; Guy N Brock; Daniel E Weeks; Eleanor Feingold
Journal:  Am J Hum Genet       Date:  2008-02-21       Impact factor: 11.025

4.  A unified framework for linkage and association analysis of quantitative traits.

Authors:  Josée Dupuis; David O Siegmund; Benjamin Yakir
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-11       Impact factor: 11.205

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

Authors:  Karen T Cuenco; Jin P Szatkiewicz; Eleanor Feingold
Journal:  Am J Hum Genet       Date:  2003-09-10       Impact factor: 11.025

Review 6.  Mapping quantitative trait loci in humans: achievements and limitations.

Authors:  Partha P Majumder; Saurabh Ghosh
Journal:  J Clin Invest       Date:  2005-06       Impact factor: 14.808

7.  Variants in the vitamin D receptor gene and asthma.

Authors:  Matthias Wjst
Journal:  BMC Genet       Date:  2005-01-15       Impact factor: 2.797

8.  Influence of genotyping error in linkage mapping for complex traits--an analytic study.

Authors:  Jérémie J P Lebrec; Hein Putter; Jeanine J Houwing-Duistermaat; Hans C van Houwelingen
Journal:  BMC Genet       Date:  2008-08-25       Impact factor: 2.797

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.