Literature DB >> 10799971

Effects of misspecification of allele frequencies on the type I error rate of model-free linkage analysis.

D M Mandal1, A F Wilson, R C Elston, K Weissbecker, B J Keats, J E Bailey-Wilson.   

Abstract

Linkage analyses of simulated quantitative trait data were performed using the Haseman-Elston (H-E) sib pair regression test to investigate the effects of inaccurate allele frequency estimates on the type I error rates of this test. Computer simulations generating a quantitative trait in nuclear families were performed using GASP [1]. Assuming no linkage, several data sets were simulated; they differed in marker allele numbers and frequencies, number of sib pairs and number of sibships. Each set of simulated data was analyzed using (1) all parental marker data, (2) half of the parental marker data, and (3) no parental marker data, using both correct and incorrect allele frequencies in the latter 2 cases. The H-E sib pair linkage method was found to be robust to misspecification of marker allele frequencies regardless of the number of alleles. Copyright 1999 S. Karger AG, Basel

Mesh:

Year:  2000        PMID: 10799971     DOI: 10.1159/000022900

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


  7 in total

1.  Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study.

Authors:  Mary F Feitosa; Ingrid B Borecki; Stephen S Rich; Donna K Arnett; Phyliss Sholinsky; Richard H Myers; Mark Leppert; Michael A Province
Journal:  Am J Hum Genet       Date:  2001-11-16       Impact factor: 11.025

2.  Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.

Authors:  Anthony M Musolf; Claire L Simpson; Theresa A Alexander; Laura Portas; Federico Murgia; Elise B Ciner; Dwight Stambolian; Joan E Bailey-Wilson
Journal:  Hum Genet       Date:  2019-03-02       Impact factor: 4.132

3.  Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment.

Authors:  Diptasri M Mandal; Alexa J M Sorant; Larry D Atwood; Alexander F Wilson; Joan E Bailey-Wilson
Journal:  BMC Genet       Date:  2006-04-20       Impact factor: 2.797

4.  Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.

Authors:  Anthony M Musolf; Bilal A Moiz; Haiming Sun; Claudio W Pikielny; Yohan Bossé; Diptasri Mandal; Mariza de Andrade; Colette Gaba; Ping Yang; Yafang Li; Ming You; Ramaswamy Govindan; Richard K Wilson; Elena Y Kupert; Marshall W Anderson; Ann G Schwartz; Susan M Pinney; Christopher I Amos; Joan E Bailey-Wilson
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2019-12-11       Impact factor: 4.254

5.  Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.

Authors:  Anthony M Musolf; Claire L Simpson; Bilal A Moiz; Kyle A Long; Laura Portas; Federico Murgia; Elise B Ciner; Dwight Stambolian; Joan E Bailey-Wilson
Journal:  Invest Ophthalmol Vis Sci       Date:  2017-07-01       Impact factor: 4.799

6.  Design considerations in a sib-pair study of linkage for susceptibility loci in cancer.

Authors:  Richard A Kerber; Christopher I Amos; Beow Y Yeap; Dianne M Finkelstein; Duncan C Thomas
Journal:  BMC Med Genet       Date:  2008-07-10       Impact factor: 2.103

7.  Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2.

Authors:  Claire L Simpson; Anthony M Musolf; Roberto Y Cordero; Jennifer B Cordero; Laura Portas; Federico Murgia; Deyana D Lewis; Candace D Middlebrooks; Elise B Ciner; Joan E Bailey-Wilson; Dwight Stambolian
Journal:  Invest Ophthalmol Vis Sci       Date:  2021-07-01       Impact factor: 4.799

  7 in total

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