Literature DB >> 11992251

Minimum-recombinant haplotyping in pedigrees.

Dajun Qian1, Lars Beckmann.   

Abstract

This article presents a six-rule algorithm for the reconstruction of multiple minimum-recombinant haplotype configurations in pedigrees. The algorithm has three major features: First, it allows exhaustive search of all possible haplotype configurations under the criterion that there are minimum recombinants between markers. Second, its computational requirement is on the order of O(J(2)L(3)) in current implementation, where J is the family size and L is the number of marker loci under analysis. Third, it applies to various pedigree structures, with and without consanguinity relationship, and allows missing alleles to be imputed, during the haplotyping process, from their identical-by-descent copies. Haplotyping examples are provided using both published and simulated data sets.

Mesh:

Year:  2002        PMID: 11992251      PMCID: PMC379131          DOI: 10.1086/340610

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


  13 in total

1.  A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.

Authors:  J A Douglas; M Boehnke; K Lange
Journal:  Am J Hum Genet       Date:  2000-03-28       Impact factor: 11.025

2.  Zero-recombinant haplotyping: applications to fine mapping using SNPs.

Authors:  J R O'Connell
Journal:  Genet Epidemiol       Date:  2000       Impact factor: 2.135

3.  Genome scan of complex traits by haplotype sharing correlation.

Authors:  D Qian; D C Thomas
Journal:  Genet Epidemiol       Date:  2001       Impact factor: 2.135

4.  Exploring haplotype sharing methods in general and isolated populations to detect gene(s) of a complex genetic trait.

Authors:  L Beckmann; C Fischer; K G Deck; I M Nolte; G te Meerman; J Chang-Claude
Journal:  Genet Epidemiol       Date:  2001       Impact factor: 2.135

5.  Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies.

Authors:  J A Douglas; M Boehnke; E Gillanders; J M Trent; S B Gruber
Journal:  Nat Genet       Date:  2001-08       Impact factor: 38.330

6.  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

7.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

8.  Simulation of pedigree genotypes by random walks.

Authors:  K Lange; S Matthysse
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

9.  A deductive method of haplotype analysis in pedigrees.

Authors:  E M Wijsman
Journal:  Am J Hum Genet       Date:  1987-09       Impact factor: 11.025

10.  A gene for episodic ataxia/myokymia maps to chromosome 12p13.

Authors:  M Litt; P Kramer; D Browne; S Gancher; E R Brunt; D Root; T Phromchotikul; C J Dubay; J Nutt
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

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  36 in total

1.  Conditional probability methods for haplotyping in pedigrees.

Authors:  Guimin Gao; Ina Hoeschele; Peter Sorensen; Fengxing Du
Journal:  Genetics       Date:  2004-08       Impact factor: 4.562

2.  Constructing the parental linkage phase and the genetic map over distances <1 cM using pooled haploid DNA.

Authors:  Dario Gasbarra; Mikko J Sillanpää
Journal:  Genetics       Date:  2005-11-19       Impact factor: 4.562

3.  Efficient inference of haplotypes from genotypes on a large animal pedigree.

Authors:  Eyal Baruch; Joel Ira Weller; Miri Cohen-Zinder; Micha Ron; Eyal Seroussi
Journal:  Genetics       Date:  2005-12-15       Impact factor: 4.562

4.  Accurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.

Authors:  Peng-Yuan Liu; Yan Lu; Hong-Wen Deng
Journal:  Genetics       Date:  2006-06-18       Impact factor: 4.562

5.  Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees.

Authors:  Ellen M Wijsman; Joseph H Rothstein; Elizabeth A Thompson
Journal:  Am J Hum Genet       Date:  2006-09-20       Impact factor: 11.025

6.  Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity.

Authors:  Kouji Maeda; Ryuji Kaji; Katsuhito Yasuno; Jamiyansuren Jambaldorj; Hiroyuki Nodera; Hiroshi Takashima; Masanori Nakagawa; Satoshi Makino; Gen Tamiya
Journal:  J Hum Genet       Date:  2007-10-02       Impact factor: 3.172

7.  A new method for haplotype inference including full-sib information.

Authors:  Xiang Dong Ding; Henner Simianer; Qin Zhang
Journal:  Genetics       Date:  2007-10-18       Impact factor: 4.562

8.  Haplotype inference in general pedigrees using the cluster variation method.

Authors:  Cornelis A Albers; Tom Heskes; Hilbert J Kappen
Journal:  Genetics       Date:  2007-07-29       Impact factor: 4.562

9.  Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels.

Authors:  Francesc Calafell; Laura Almasy; Maria Sabater-Lleal; Alfonso Buil; Carolina Mordillo; Anna Ramírez-Soriano; Martin Sikora; Juan Carlos Souto; John Blangero; Jordi Fontcuberta; José Manuel Soria
Journal:  Hum Mol Genet       Date:  2009-11-23       Impact factor: 6.150

Review 10.  Haplotyping methods for pedigrees.

Authors:  Guimin Gao; David B Allison; Ina Hoeschele
Journal:  Hum Hered       Date:  2009-01-27       Impact factor: 0.444

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