Literature DB >> 11713418

The null distribution of the heterogeneity lod score does depend on the assumed genetic model for the trait.

J Huang1, V J Vieland.   

Abstract

It is well known that the asymptotic null distribution of the homogeneity lod score (LOD) does not depend on the genetic model specified in the analysis. When appropriately rescaled, the LOD is asymptotically distributed as 0.5 chi(2)(0) + 0.5 chi(2)(1), regardless of the assumed trait model. However, because locus heterogeneity is a common phenomenon, the heterogeneity lod score (HLOD), rather than the LOD itself, is often used in gene mapping studies. We show here that, in contrast with the LOD, the asymptotic null distribution of the HLOD does depend upon the genetic model assumed in the analysis. In affected sib pair (ASP) data, this distribution can be worked out explicitly as (0.5 - c)chi(2)(0) + 0.5chi(2)(1) + cchi(2)(2), where c depends on the assumed trait model. E.g., for a simple dominant model (HLOD/D), c is a function of the disease allele frequency p: for p = 0.01, c = 0.0006; while for p = 0.1, c = 0.059. For a simple recessive model (HLOD/R), c = 0.098 independently of p. This latter (recessive) distribution turns out to be the same as the asymptotic distribution of the MLS statistic under the possible triangle constraint, which is asymptotically equivalent to the HLOD/R. The null distribution of the HLOD/D is close to that of the LOD, because the weight c on the chi(2)(2) component is small. These results mean that the cutoff value for a test of size alpha will tend to be smaller for the HLOD/D than the HLOD/R. For example, the alpha = 0.0001 cutoff (on the lod scale) for the HLOD/D with p = 0.05 is 3.01, while for the LOD it is 3.00, and for the HLOD/R it is 3.27. For general pedigrees, explicit analytical expression of the null HLOD distribution does not appear possible, but it will still depend on the assumed genetic model. Copyright 2001 S. Karger AG, Basel

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Year:  2001        PMID: 11713418     DOI: 10.1159/000053379

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  4 in total

1.  Regression models for linkage heterogeneity applied to familial prostate cancer.

Authors:  D J Schaid; S K McDonnell; S N Thibodeau
Journal:  Am J Hum Genet       Date:  2001-04-13       Impact factor: 11.025

2.  HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity.

Authors:  Susan E Hodge; Veronica J Vieland; David A Greenberg
Journal:  Am J Hum Genet       Date:  2002-02       Impact factor: 11.025

3.  Distribution of model-based multipoint heterogeneity lod scores.

Authors:  Chao Xing; Nathan Morris; Guan Xing
Journal:  Genet Epidemiol       Date:  2010-12       Impact factor: 2.135

4.  Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.

Authors:  John M Darlow; Rebecca Darlay; Mark G Dobson; Aisling Stewart; Pimphen Charoen; Jennifer Southgate; Simon C Baker; Yaobo Xu; Manuela Hunziker; Heather J Lambert; Andrew J Green; Mauro Santibanez-Koref; John A Sayer; Timothy H J Goodship; Prem Puri; Adrian S Woolf; Rajko B Kenda; David E Barton; Heather J Cordell
Journal:  Sci Rep       Date:  2017-11-06       Impact factor: 4.379

  4 in total

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