Literature DB >> 8224802

Chromosome-based method for rapid computer simulation in human genetic linkage analysis.

J D Terwilliger1, M Speer, J Ott.   

Abstract

Computer-based simulation has been an important method in human linkage analysis for a long time. Typically, such analyses have been performed by simulating a set of linked markers according to the intermarker recombination fractions, under the assumption of no genetic interference. A novel approach is proposed in which such simulations can be performed using chromosome-based methods, rather than traditional recombination fraction-based methods. We propose simulating pedigree data using a crossover formation (CF) process to generate the number of crossovers and their locations in Morgans along the entire length of a chromosome. By this method, one can generate simulated multilocus data for any number of loci on a chromosome much more efficiently than with the currently available methods like those used in the SLINK or SIMLINK programs. Further, interference can be incorporated directly in this method, which is not possible with existing packages.

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Year:  1993        PMID: 8224802     DOI: 10.1002/gepi.1370100402

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  42 in total

1.  Data mining applied to linkage disequilibrium mapping.

Authors:  H T Toivonen; P Onkamo; K Vasko; V Ollikainen; P Sevon; H Mannila; M Herr; J Kere
Journal:  Am J Hum Genet       Date:  2000-06-09       Impact factor: 11.025

2.  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

3.  Genetic maps of microsatellite and single-nucleotide polymorphism markers: are the distances accurate?

Authors:  Suzanne M Leal
Journal:  Genet Epidemiol       Date:  2003-05       Impact factor: 2.135

4.  A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

Authors:  Tara C Matise; Ravi Sachidanandam; Andrew G Clark; Leonid Kruglyak; Ellen Wijsman; Jerzy Kakol; Steven Buyske; Buena Chui; Patrick Cohen; Claudia de Toma; Margaret Ehm; Stephen Glanowski; Chunsheng He; Jeremy Heil; Kyriacos Markianos; Ivy McMullen; Margaret A Pericak-Vance; Arkadiy Silbergleit; Lincoln Stein; Michael Wagner; Alexander F Wilson; Jeffrey D Winick; Emily S Winn-Deen; Carl T Yamashiro; Howard M Cann; Eric Lai; Arthur L Holden
Journal:  Am J Hum Genet       Date:  2003-07-03       Impact factor: 11.025

5.  Linkage analysis of alternative anxiety phenotypes in multiply affected panic disorder families.

Authors:  Abby J Fyer; Ramiro Costa; Fatemeh Haghighi; Mark W Logue; James A Knowles; Myrna M Weissman; Susan E Hodge; Steven P Hamilton
Journal:  Psychiatr Genet       Date:  2012-06       Impact factor: 2.458

6.  SimPed: a simulation program to generate haplotype and genotype data for pedigree structures.

Authors:  Suzanne M Leal; Kai Yan; Bertram Müller-Myhsok
Journal:  Hum Hered       Date:  2005-10-13       Impact factor: 0.444

7.  Using linkage genome scans to improve power of association in genome scans.

Authors:  Kathryn Roeder; Silvi-Alin Bacanu; Larry Wasserman; B Devlin
Journal:  Am J Hum Genet       Date:  2006-01-03       Impact factor: 11.025

8.  Imprinting detection by extending a regression-based QTL analysis method.

Authors:  Olga Y Gorlova; Lei Lei; Dakai Zhu; Shih-Feng Weng; Sanjay Shete; Yiqun Zhang; Wei-Dong Li; R Arlen Price; Christopher I Amos
Journal:  Hum Genet       Date:  2007-06-12       Impact factor: 4.132

9.  Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).

Authors:  Kim L McBride; Gloria A Zender; Sara M Fitzgerald-Butt; Daniel Koehler; Andres Menesses-Diaz; Susan Fernbach; Kwanghyuk Lee; Jeffrey A Towbin; Suzanne Leal; John W Belmont
Journal:  Eur J Hum Genet       Date:  2009-01-14       Impact factor: 4.246

10.  Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

Authors:  Matthew N Ogdie; Simon E Fisher; May Yang; Janeen Ishii; Clyde Francks; Sandra K Loo; Rita M Cantor; James T McCracken; James J McGough; Susan L Smalley; Stanley F Nelson
Journal:  Am J Hum Genet       Date:  2004-08-03       Impact factor: 11.025

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