Literature DB >> 3341384

A new statistical test for linkage heterogeneity.

N Risch1.   

Abstract

A new, statistical test for linkage heterogeneity is described. It is a likelihood-ratio test based on a beta distribution for the prior distribution of the recombination fraction among families (or individuals). The null distribution for this statistic (called the B-test) is derived under a broad range of circumstances. Two other heterogeneity test statistics--the admixture test or A-test first described by Smith and Morton's test (here referred to as the K-test)--are also examined. The probability distribution for the K-test statistic is very sensitive to family size, whereas the other two statistics are not. All three statistics are somewhat sensitive to the magnitude of the recombination fraction theta. Critical values for each of the test statistics are given. A conservative approximation for both the A-test and B-test is given by a chi 2 distribution when P/2 instead of P is used for the observed significance level. In terms of power, the B-test performs best among the three tests over a broad range of alternate heterogeneity hypotheses--except for the specific case of admixture with loose linkage, in which the A-test performs best. Overall, the difference in power among the three tests is not large. An application to some recently published data on the fragile-X syndrome and X-chromosome markers is given.

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Year:  1988        PMID: 3341384      PMCID: PMC1715251     

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


  7 in total

1.  TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS.

Authors:  C A SMITH
Journal:  Ann Hum Genet       Date:  1963-11       Impact factor: 1.670

2.  The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1956-06       Impact factor: 11.025

3.  Counting methods (EM algorithm) in human pedigree analysis: linkage and segregation analysis.

Authors:  J Ott
Journal:  Ann Hum Genet       Date:  1977-05       Impact factor: 1.670

4.  X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data.

Authors:  N Risch; M Baron
Journal:  Ann Hum Genet       Date:  1982-05       Impact factor: 1.670

5.  Variability of human linkage data.

Authors:  D C Rao; B J Keats; N E Morton; S Yee; R Lew
Journal:  Am J Hum Genet       Date:  1978-09       Impact factor: 11.025

6.  The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity.

Authors:  S E Hodge; C E Anderson; K Neiswanger; R S Sparkes; D L Rimoin
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

7.  Further evidence for genetic heterogeneity in the fragile X syndrome.

Authors:  W T Brown; E C Jenkins; A C Gross; C B Chan; M S Krawczun; C J Duncan; S L Sklower; G S Fisch
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

  7 in total
  14 in total

Review 1.  Current perspectives on the genetics of unipolar depression.

Authors:  S O Moldin; T Reich; J P Rice
Journal:  Behav Genet       Date:  1991-05       Impact factor: 2.805

2.  An estimating function approach to linkage heterogeneity.

Authors:  He Gao; Ying Zhou; Weijun Ma; Haidong Liu; Linan Zhao
Journal:  J Genet       Date:  2013-12       Impact factor: 1.166

3.  Linkage of familial breast cancer to chromosome 17q21 may not be restricted to early-onset disease.

Authors:  P Margaritte; C Bonaiti-Pellie; M C King; F Clerget-Darpoux
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

4.  A genomewide linkage study of preeclampsia/eclampsia reveals evidence for a candidate region on 4q.

Authors:  G A Harrison; K E Humphrey; N Jones; R Badenhop; G Guo; G Elakis; J A Kaye; R J Turner; M Grehan; A N Wilton; S P Brennecke; D W Cooper
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

5.  A combined test of linkage heterogeneity.

Authors:  D R Goldstein
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

6.  A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4.

Authors:  A A Puca; M J Daly; S J Brewster; T C Matise; J Barrett; M Shea-Drinkwater; S Kang; E Joyce; J Nicoli; E Benson; L M Kunkel; T Perls
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-27       Impact factor: 11.205

7.  Evidence for individual and between-family variability of the recombination rate in cattle.

Authors:  H Simianer; J Szyda; G Ramon; S Lien
Journal:  Mamm Genome       Date:  1997       Impact factor: 2.957

8.  A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.

Authors:  C M van Duijn; L Hendriks; L A Farrer; H Backhovens; M Cruts; A Wehnert; A Hofman; C Van Broeckhoven
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

9.  Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Authors:  L A Farrer; K M Grundfast; J Amos; K S Arnos; J H Asher; P Beighton; S R Diehl; J Fex; C Foy; T B Friedman
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

10.  Comparative recombination distances among Zea mays L. inbreds, wide crosses and interspecific hybrids.

Authors:  C G Williams; M M Goodman; C W Stuber
Journal:  Genetics       Date:  1995-12       Impact factor: 4.562

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