Literature DB >> 8056435

Avoiding recomputation in linkage analysis.

A A Schäffer1, S K Gupta, K Shriram, R W Cottingham.   

Abstract

We describe four improvements we have implemented in a version of the genetic linkage analysis programs in the LINKAGE package: subdivision of recombination classes, better handling of loops, better coordination between the optimization and output routines, and a checkpointing facility. The unifying theme for all the improvements is to store a small amount of data to avoid expensive recomputation of known results. The subdivision of recombination classes improves on a method of Lathrop and Lalouel [Am J Hum Genet 1988;42:498-505]. The new method of handling loops extends a proposal of Lange and Elston [Hum Hered 1975;25:95-105] for loopless pedigrees with multiple nuclear families at the earliest generation. From a practical point of view, the most important improvement may be the checkpointing facility which allows the user to carry out linkage computations that are much longer than the mean-time-to-failure of the underlying computer.

Mesh:

Year:  1994        PMID: 8056435     DOI: 10.1159/000154222

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


  252 in total

1.  Blocking Gibbs sampling for linkage analysis in large pedigrees with many loops.

Authors:  C S Jensen; A Kong
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

2.  Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.

Authors:  M C Lanasa; W A Hogge; C Kubik; J Blancato; E P Hoffman
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

3.  Assessment of parent-of-origin effects in linkage analysis of quantitative traits.

Authors:  R L Hanson; S Kobes; R S Lindsay; W C Knowler
Journal:  Am J Hum Genet       Date:  2001-03-13       Impact factor: 11.025

4.  Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.

Authors:  S Goobie; M Popovic; J Morrison; L Ellis; H Ginzberg; G R Boocock; N Ehtesham; C Bétard; C G Brewer; N M Roslin; T J Hudson; K Morgan; T M Fujiwara; P R Durie; J M Rommens
Journal:  Am J Hum Genet       Date:  2001-03-15       Impact factor: 11.025

5.  Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter.

Authors:  W Zhang; R Amir; D W Stockton; I B Van Den Veyver; C A Bacino; H Y Zoghbi
Journal:  Am J Hum Genet       Date:  2000-03-17       Impact factor: 11.025

Review 6.  Gene mapping by linkage and association analysis.

Authors:  R E March
Journal:  Mol Biotechnol       Date:  1999-12-01       Impact factor: 2.695

7.  Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

Authors:  C M Greenwood; T M Fujiwara; L J Boothroyd; M A Miller; D Frappier; E A Fanning; E Schurr; K Morgan
Journal:  Am J Hum Genet       Date:  2000-07-05       Impact factor: 11.025

8.  Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.

Authors:  N Laurin; J P Brown; A Lemainque; A Duchesne; D Huot; Y Lacourcière; G Drapeau; J Verreault; V Raymond; J Morissette
Journal:  Am J Hum Genet       Date:  2001-07-25       Impact factor: 11.025

9.  A genomewide search for type 2 diabetes-susceptibility genes in indigenous Australians.

Authors:  Frances Busfield; David L Duffy; Janine B Kesting; Shelley M Walker; Paul K Lovelock; David Good; Heather Tate; Denise Watego; Maureen Marczak; Noel Hayman; Joanne T E Shaw
Journal:  Am J Hum Genet       Date:  2001-12-12       Impact factor: 11.025

10.  Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families.

Authors:  Aino Soro; Päivi Pajukanta; Heidi E Lilja; Kati Ylitalo; Tero Hiekkalinna; Markus Perola; Rita M Cantor; Jorma S A Viikari; Marja-Riitta Taskinen; Leena Peltonen
Journal:  Am J Hum Genet       Date:  2002-03-12       Impact factor: 11.025

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