Literature DB >> 8317490

Faster sequential genetic linkage computations.

R W Cottingham1, R M Idury, A A Schäffer.   

Abstract

Linkage analysis using maximum-likelihood estimation is a powerful tool for locating genes. As available data sets have grown, the computation required for analysis has grown exponentially and become a significant impediment. Others have previously shown that parallel computation is applicable to linkage analysis and can yield order-of-magnitude improvements in speed. In this paper, we demonstrate that algorithmic modifications can also yield order-of-magnitude improvements, and sometimes much more. Using the software package LINKAGE, we describe a variety of algorithmic improvements that we have implemented, demonstrating both how these techniques are applied and their power. Experiments show that these improvements speed up the programs by an order of magnitude, on problems of moderate and large size. All improvements were made only in the combinatorial part of the code, without restoring to parallel computers. These improvements synthesize biological principles with computer science techniques, to effectively restructure the time-consuming computations in genetic linkage analysis.

Mesh:

Year:  1993        PMID: 8317490      PMCID: PMC1682239     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  12 in total

1.  Extensions to pedigree analysis I. Likehood calculations for simple and complex pedigrees.

Authors:  K Lange; R C Elston
Journal:  Hum Hered       Date:  1975       Impact factor: 0.444

2.  Fast computation of genetic likelihoods on human pedigree data.

Authors:  T M Goradia; K Lange; P L Miller; P M Nadkarni
Journal:  Hum Hered       Date:  1992       Impact factor: 0.444

3.  Parallelizing genetic linkage analysis: a case study for applying parallel computation in molecular biology.

Authors:  P L Miller; P Nadkarni; J E Gelernter; N Carriero; A J Pakstis; K K Kidd
Journal:  Comput Biomed Res       Date:  1991-06

4.  Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome.

Authors:  J Dausset; H Cann; D Cohen; M Lathrop; J M Lalouel; R White
Journal:  Genomics       Date:  1990-03       Impact factor: 5.736

5.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

6.  A general model for the genetic analysis of pedigree data.

Authors:  R C Elston; J Stewart
Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

7.  An algorithm for automatic genotype elimination.

Authors:  K Lange; T M Goradia
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

8.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

9.  Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Authors:  S H Blanton; J R Heckenlively; A W Cottingham; J Friedman; L A Sadler; M Wagner; L H Friedman; S P Daiger
Journal:  Genomics       Date:  1991-12       Impact factor: 5.736

10.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

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  480 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.  A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Authors:  K Fukushima; N Kasai; Y Ueki; K Nishizaki; K Sugata; S Hirakawa; A Masuda; M Gunduz; Y Ninomiya; Y Masuda; M Sato; W T McGuirt; P Coucke; G Van Camp; R J Smith
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

4.  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

5.  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

6.  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

7.  Efficient multipoint linkage analysis through reduction of inheritance space.

Authors:  K Markianos; M J Daly; L Kruglyak
Journal:  Am J Hum Genet       Date:  2001-03-14       Impact factor: 11.025

8.  Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.

Authors:  L Cuisset; J P Drenth; J M Berthelot; A Meyrier; G Vaudour; R A Watts; D G Scott; A Nicholls; S Pavek; C Vasseur; J S Beckmann; M Delpech; G Grateau
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

9.  Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

Authors:  P F Worth; P Giunti; C Gardner-Thorpe; P H Dixon; M B Davis; N W Wood
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

10.  Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.

Authors:  H H Göring; J D Terwilliger
Journal:  Am J Hum Genet       Date:  2000-03-23       Impact factor: 11.025

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