Literature DB >> 9463802

Automatic selection of loop breakers for genetic linkage analysis.

A Becker1, D Geiger, A A Schäffer.   

Abstract

Pedigree loops pose a difficult computational challenge in genetic linkage analysis. The most popular linkage analysis package, LINKAGE, uses an algorithm that converts a looped pedigree into a loopless pedigree, which is traversed many times. The conversion is controlled by user selection of individuals to act as loop breakers. The selection of loop breakers has significant impact on the running time of the subsequent linkage analysis. We have automated the process of selecting loop breakers, implemented a hybrid algorithm for it in the FASTLINK version of LINKAGE, and tested it on many real pedigrees with excellent performance. We point out that there is no need to break each loop by a distinct individual because, with minor modification to the algorithms in LINKAGE/FASTLINK, a single individual that participates in multiple marriages can serve as a loop breaker for several loops. Our algorithm for finding loop breakers, called LOOPBREAKER, is a combination of: (1) a new algorithm that is guaranteed to be optimal in the special case of pedigrees with no multiple marriages and (2) an adaptation of a known algorithm for breaking loops in general graphs. The contribution of this work is the adaptation of abstract methods from computer science to a challenging problem in genetics.

Mesh:

Year:  1998        PMID: 9463802     DOI: 10.1159/000022781

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


  18 in total

1.  An optimal algorithm for automatic genotype elimination.

Authors:  J R O'Connell; D E Weeks
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.

Authors:  Simeon A Boyadjiev; Cristina M Justice; Wafaa Eyaid; Victor A McKusick; Ralph S Lachman; Arnab B Chowdry; Monzer Jabak; Johan Zwaan; Alexander F Wilson; Ethylin Wang Jabs
Journal:  Hum Genet       Date:  2003-04-03       Impact factor: 4.132

3.  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

4.  Online system for faster multipoint linkage analysis via parallel execution on thousands of personal computers.

Authors:  M Silberstein; A Tzemach; N Dovgolevsky; M Fishelson; A Schuster; D Geiger
Journal:  Am J Hum Genet       Date:  2006-05-01       Impact factor: 11.025

5.  Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Authors:  C Bétard; A Rasquin-Weber; C Brewer; E Drouin; S Clark; A Verner; C Darmond-Zwaig; J Fortin; J Mercier; P Chagnon; T M Fujiwara; K Morgan; A Richter; T J Hudson; G A Mitchell
Journal:  Am J Hum Genet       Date:  2000-05-11       Impact factor: 11.025

6.  PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals.

Authors:  Tero Hiekkalinna; Alejandro A Schäffer; Brian Lambert; Petri Norrgrann; Harald H H Göring; Joseph D Terwilliger
Journal:  Hum Hered       Date:  2011-07-28       Impact factor: 0.444

7.  A novel nemaline myopathy in the Amish caused by a mutation in troponin T1.

Authors:  J J Johnston; R I Kelley; T O Crawford; D H Morton; R Agarwala; T Koch; A A Schäffer; C A Francomano; L G Biesecker
Journal:  Am J Hum Genet       Date:  2000-08-21       Impact factor: 11.025

8.  A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

Authors:  L Gieser; R Fujita; H H Göring; J Ott; D R Hoffman; A V Cideciyan; D G Birch; S G Jacobson; A Swaroop
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

9.  Canine Imerslund-Gräsbeck syndrome maps to a region orthologous to HSA14q.

Authors:  Qianchuan He; John C Fyfe; Alejandro A Schäffer; Adam Kilkenney; Petra Werner; Ewen F Kirkness; Paula S Henthorn
Journal:  Mamm Genome       Date:  2003-11       Impact factor: 2.957

10.  Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter.

Authors:  M Hirano; J Garcia-de-Yebenes; A C Jones; I Nishino; S DiMauro; J R Carlo; A N Bender; A F Hahn; L M Salberg; D E Weeks; T G Nygaard
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

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