Literature DB >> 7668271

Complete multipoint sib-pair analysis of qualitative and quantitative traits.

L Kruglyak1, E S Lander.   

Abstract

Sib-pair analysis is an increasingly important tool for genetic dissection of complex traits. Current methods for sib-pair analysis are primarily based on studying individual genetic markers one at a time and thus fail to use the full inheritance information provided by multipoint linkage analysis. In this paper, we describe how to extract the complete multipoint inheritance information for each sib pair. We then describe methods that use this information to map loci affecting traits, thereby providing a unified approach to both qualitative and quantitative traits. Specifically, complete multipoint approaches are presented for (1) exclusion mapping of qualitative traits; (2) maximum-likelihood mapping of qualitative traits; (3) information-content mapping, showing the extent to which all inheritance information has been extracted at each location in the genome; and (4) quantitative-trait mapping, by two parametric methods and one nonparametric method. In addition, we explore the effects of marker density, marker polymorphism, and availability of parents on the information content of a study. We have implemented the analysis methods in a new computer package, MAPMAKER/SIBS. With this computer package, complete multipoint analysis with dozens of markers in hundreds of sib pairs can be carried out in minutes.

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Year:  1995        PMID: 7668271      PMCID: PMC1801561     

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


  19 in total

1.  The 1993-94 Généthon human genetic linkage map.

Authors:  G Gyapay; J Morissette; A Vignal; C Dib; C Fizames; P Millasseau; S Marc; G Bernardi; M Lathrop; J Weissenbach
Journal:  Nat Genet       Date:  1994-06       Impact factor: 38.330

2.  Multipoint interval mapping of quantitative trait loci, using sib pairs.

Authors:  D W Fulker; S S Cherny; L R Cardon
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

3.  A nonparametric approach for mapping quantitative trait loci.

Authors:  L Kruglyak; E S Lander
Journal:  Genetics       Date:  1995-03       Impact factor: 4.562

4.  A sib-pair approach to interval mapping of quantitative trait loci.

Authors:  D W Fulker; L R Cardon
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

5.  Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

Authors:  L Kruglyak; M J Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

6.  Quantitative trait locus for reading disability on chromosome 6.

Authors:  L R Cardon; S D Smith; D W Fulker; W J Kimberling; B F Pennington; J C DeFries
Journal:  Science       Date:  1994-10-14       Impact factor: 47.728

Review 7.  Genetic dissection of complex traits.

Authors:  E S Lander; N J Schork
Journal:  Science       Date:  1994-09-30       Impact factor: 47.728

8.  Integrated human genome-wide maps constructed using the CEPH reference panel.

Authors:  K H Buetow; J L Weber; S Ludwigsen; T Scherpbier-Heddema; G M Duyk; V C Sheffield; Z Wang; J C Murray
Journal:  Nat Genet       Date:  1994-04       Impact factor: 38.330

9.  The power of interval mapping of quantitative trait loci, using selected sib pairs.

Authors:  L R Cardon; D W Fulker
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

10.  A genome-wide search for human type 1 diabetes susceptibility genes.

Authors:  J L Davies; Y Kawaguchi; S T Bennett; J B Copeman; H J Cordell; L E Pritchard; P W Reed; S C Gough; S C Jenkins; S M Palmer
Journal:  Nature       Date:  1994-09-08       Impact factor: 49.962

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  207 in total

1.  Replication of linkage studies of complex traits: an examination of variation in location estimates.

Authors:  S B Roberts; C J MacLean; M C Neale; L J Eaves; K S Kendler
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

2.  A random model approach to mapping quantitative trait loci for complex binary traits in outbred populations.

Authors:  N Yi; S Xu
Journal:  Genetics       Date:  1999-10       Impact factor: 4.562

3.  On a randomization procedure in linkage analysis.

Authors:  H Zhao; K R Merikangas; K K Kidd
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

4.  Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves disease.

Authors:  S H Pearce; B Vaidya; H Imrie; P Perros; W F Kelly; A D Toft; M I McCarthy; E T Young; P Kendall-Taylor
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

5.  A general conditional-logistic model for affected-relative-pair linkage studies.

Authors:  J M Olson
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

6.  Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease.

Authors:  J Hampe; N J Lynch; S Daniels; S Bridger; A J Macpherson; P Stokkers; A Forbes; J E Lennard-Jones; C G Mathew; M E Curran; S Schreiber
Journal:  Gut       Date:  2001-02       Impact factor: 23.059

7.  Transformation of sib-pair values for the Haseman-Elston method.

Authors:  D Wang; S Lin; R Cheng; X Gao; F A Wright
Journal:  Am J Hum Genet       Date:  2001-04-17       Impact factor: 11.025

8.  Model-free linkage analysis with covariates confirms linkage of prostate cancer to chromosomes 1 and 4.

Authors:  K A Goddard; J S Witte; B K Suarez; W J Catalona; J M Olson
Journal:  Am J Hum Genet       Date:  2001-04-13       Impact factor: 11.025

9.  A paradigm for finding genes for a complex human trait: polycystic ovary syndrome and follistatin.

Authors:  K Odunsi; K K Kidd
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-20       Impact factor: 11.205

10.  Contribution of the MHC region to the familial risk of coeliac disease.

Authors:  S Bevan; S Popat; C P Braegger; A Busch; D O'Donoghue; K Falth-Magnusson; A Ferguson; A Godkin; L Hogberg; G Holmes; K B Hosie; P D Howdle; H Jenkins; D Jewell; S Johnston; N P Kennedy; G Kerr; P Kumar; R F Logan; A H Love; M Marsh; C J Mulder; K Sjoberg; L Stenhammer; J Walker-Smith; A M Marossy; R S Houlston
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

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