Literature DB >> 7847388

Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

L Kruglyak1, M J Daly, E S Lander.   

Abstract

Homozygosity mapping is a powerful strategy for mapping rare recessive traits in children of consanguineous marriages. Practical applications of this strategy are currently limited by the inability of conventional linkage analysis software to compute, in reasonable time, multipoint LOD scores for pedigrees with inbreeding loops. We have developed a new algorithm for rapid multipoint likelihood calculations in small pedigrees, including those with inbreeding loops. The running time of the algorithm grows, at most, linearly with the number of loci considered simultaneously. The running time is not sensitive to the presence of inbreeding loops, missing genotype information, and highly polymorphic loci. We have incorporated this algorithm into a software package, MAPMAKER/HOMOZ, that allows very rapid multipoint mapping of disease genes in nuclear families, including homozygosity mapping. Multipoint analysis with dozens of markers can be carried out in minutes on a personal workstation.

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Mesh:

Year:  1995        PMID: 7847388      PMCID: PMC1801139     

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


  19 in total

1.  Strategies for characterizing highly polymorphic markers in human gene mapping.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

2.  Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16.

Authors:  E Pras; I Aksentijevich; L Gruberg; J E Balow; L Prosen; M Dean; A D Steinberg; M Pras; D L Kastner
Journal:  N Engl J Med       Date:  1992-06-04       Impact factor: 91.245

3.  A mapped set of DNA markers for human chromosome 17.

Authors:  Y Nakamura; M Lathrop; P O'Connell; M Leppert; D Barker; E Wright; M Skolnick; S Kondoleon; M Litt; J M Lalouel
Journal:  Genomics       Date:  1988-05       Impact factor: 5.736

4.  Homozygosity mapping: familiarity breeds debility.

Authors:  M Farrall
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

5.  Faster sequential genetic linkage computations.

Authors:  R W Cottingham; R M Idury; A A Schäffer
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

6.  Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies.

Authors:  I Aksentijevich; E Pras; L Gruberg; Y Shen; K Holman; S Helling; L Prosen; G R Sutherland; R I Richards; M Ramsburg
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

7.  Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?

Authors:  I Aksentijevich; L Gruberg; E Pras; J E Balow; M Kovo; E Gazit; M Dean; M Pras; D L Kastner
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

8.  MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations.

Authors:  E S Lander; P Green; J Abrahamson; A Barlow; M J Daly; S E Lincoln; L A Newberg; L Newburg
Journal:  Genomics       Date:  1987-10       Impact factor: 5.736

9.  Genetic linkage of Werner's syndrome to five markers on chromosome 8.

Authors:  M Goto; M Rubenstein; J Weber; K Woods; D Drayna
Journal:  Nature       Date:  1992-02-20       Impact factor: 49.962

10.  Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping.

Authors:  C Ben Hamida; N Doerflinger; S Belal; C Linder; L Reutenauer; C Dib; G Gyapay; A Vignal; D Le Paslier; D Cohen
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

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  75 in total

1.  Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15.

Authors:  C R Jamieson; C Govaerts; M J Abramowicz
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

2.  Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.

Authors:  S Chavanas; C Garner; C Bodemer; M Ali; D H Teillac; J Wilkinson; J L Bonafé; M Paradisi; D P Kelsell; S i Ansai; Y Mitsuhashi; M Larrègue; I M Leigh; J I Harper; A Taïeb; Y d Prost; L R Cardon; A Hovnanian
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

3.  Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization.

Authors:  K Strauch; R Fimmers; T Kurz; K A Deichmann; T F Wienker; M P Baur
Journal:  Am J Hum Genet       Date:  2000-05-04       Impact factor: 11.025

4.  Detection and integration of genotyping errors in statistical genetics.

Authors:  Eric Sobel; Jeanette C Papp; Kenneth Lange
Journal:  Am J Hum Genet       Date:  2002-01-08       Impact factor: 11.025

5.  Likelihood formulation of parent-of-origin effects on segregation analysis, including ascertainment.

Authors:  Fatemeh Haghighi; Susan E Hodge
Journal:  Am J Hum Genet       Date:  2001-11-30       Impact factor: 11.025

6.  Bayesian mapping of multiple quantitative trait loci from incomplete outbred offspring data.

Authors:  M J Sillanpää; E Arjas
Journal:  Genetics       Date:  1999-04       Impact factor: 4.562

7.  Evidence for asthma susceptibility genes on chromosome 11 in an African-American population.

Authors:  Shau-Ku Huang; Rasika A Mathias; Eva Ehrlich; Beverly Plunkett; Xin Liu; Garry R Cutting; Xin-Jing Wang; Xiao-Dong Li; Alkis Togias; Kathleen C Barnes; Floyd Malveaux; Stephen Rich; Beverly Mellen; Ethan Lange; Terri H Beaty
Journal:  Hum Genet       Date:  2003-03-27       Impact factor: 4.132

8.  Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

Authors:  J M Bork; L M Peters; S Riazuddin; S L Bernstein; Z M Ahmed; S L Ness; R Polomeno; A Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Z Ahmed; S N Khan; V M Kaloustian; X C Li; A Lalwani; S Riazuddin; M Bitner-Glindzicz; W E Nance; X Z Liu; G Wistow; R J Smith; A J Griffith; E R Wilcox; T B Friedman; R J Morell
Journal:  Am J Hum Genet       Date:  2000-11-21       Impact factor: 11.025

9.  Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.

Authors:  P Ianakiev; M J Daly; S P Toledo; M G Cavalcanti; J C Neto; E L Silveira; A Freire-Maia; P Heutink; M W Kilpatrick; P Tsipouras
Journal:  Am J Hum Genet       Date:  2000-11-22       Impact factor: 11.025

Review 10.  Linkage analysis in the next-generation sequencing era.

Authors:  Joan E Bailey-Wilson; Alexander F Wilson
Journal:  Hum Hered       Date:  2011-12-23       Impact factor: 0.444

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