Literature DB >> 12386835

Haplotype inference in random population samples.

Shin Lin1, David J Cutler, Michael E Zwick, Aravinda Chakravarti.   

Abstract

Contemporary genotyping and sequencing methods do not provide information on linkage phase in diploid organisms. The application of statistical methods to infer and reconstruct linkage phase in samples of diploid sequences is a potentially time- and labor-saving method. The Stephens-Smith-Donnelly (SSD) algorithm is one such method, which incorporates concepts from population genetics theory in a Markov chain-Monte Carlo technique. We applied a modified SSD method, as well as the expectation-maximization and partition-ligation algorithms, to sequence data from eight loci spanning >1 Mb on the human X chromosome. We demonstrate that the accuracy of the modified SSD method is better than that of the other algorithms and is superior in terms of the number of sites that may be processed. Also, we find phase reconstructions by the modified SSD method to be highly accurate over regions with high linkage disequilibrium (LD). If only polymorphisms with a minor allele frequency >0.2 are analyzed and scored according to the fraction of neighbor relations correctly called, reconstructions are 95.2% accurate over entire 100-kb stretches and are 98.6% accurate within blocks of high LD.

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Year:  2002        PMID: 12386835      PMCID: PMC385088          DOI: 10.1086/344347

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


  20 in total

1.  A new statistical method for haplotype reconstruction from population data.

Authors:  M Stephens; N J Smith; P Donnelly
Journal:  Am J Hum Genet       Date:  2001-03-09       Impact factor: 11.025

Review 2.  A chronology of fine-scale gene mapping by linkage disequilibrium.

Authors:  L C Lazzeroni
Journal:  Stat Methods Med Res       Date:  2001-02       Impact factor: 3.021

3.  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

4.  Comparisons of two methods for haplotype reconstruction and haplotype frequency estimation from population data.

Authors:  S Zhang; A J Pakstis; K K Kidd; H Zhao
Journal:  Am J Hum Genet       Date:  2001-10       Impact factor: 11.025

5.  Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.

Authors:  J D Rioux; M J Daly; M S Silverberg; K Lindblad; H Steinhart; Z Cohen; T Delmonte; K Kocher; K Miller; S Guschwan; E J Kulbokas; S O'Leary; E Winchester; K Dewar; T Green; V Stone; C Chow; A Cohen; D Langelier; G Lapointe; D Gaudet; J Faith; N Branco; S B Bull; R S McLeod; A M Griffiths; A Bitton; G R Greenberg; E S Lander; K A Siminovitch; T J Hudson
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

6.  High-resolution haplotype structure in the human genome.

Authors:  M J Daly; J D Rioux; S F Schaffner; T J Hudson; E S Lander
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

7.  Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex.

Authors:  A J Jeffreys; L Kauppi; R Neumann
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

8.  Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data.

Authors:  D Fallin; N J Schork
Journal:  Am J Hum Genet       Date:  2000-08-22       Impact factor: 11.025

9.  A DNA polymorphism discovery resource for research on human genetic variation.

Authors:  F S Collins; L D Brooks; A Chakravarti
Journal:  Genome Res       Date:  1998-12       Impact factor: 9.043

10.  Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.

Authors:  J P Hugot; M Chamaillard; H Zouali; S Lesage; J P Cézard; J Belaiche; S Almer; C Tysk; C A O'Morain; M Gassull; V Binder; Y Finkel; A Cortot; R Modigliani; P Laurent-Puig; C Gower-Rousseau; J Macry; J F Colombel; M Sahbatou; G Thomas
Journal:  Nature       Date:  2001-05-31       Impact factor: 49.962

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  61 in total

1.  A comparison of bayesian methods for haplotype reconstruction from population genotype data.

Authors:  Matthew Stephens; Peter Donnelly
Journal:  Am J Hum Genet       Date:  2003-10-20       Impact factor: 11.025

2.  Haplotype and missing data inference in nuclear families.

Authors:  Shin Lin; Aravinda Chakravarti; David J Cutler
Journal:  Genome Res       Date:  2004-07-15       Impact factor: 9.043

3.  Identifying the susceptibility gene(s) in a set of trait-linked genes using genotype data.

Authors:  Ao Yuan; Guanjie Chen; Yuanxiu Chen; Charles Rotimi; George E Bonney
Journal:  Genetics       Date:  2004-07       Impact factor: 4.562

4.  Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies.

Authors:  Kui Zhang; Zhaohui S Qin; Jun S Liu; Ting Chen; Michael S Waterman; Fengzhu Sun
Journal:  Genome Res       Date:  2004-04-12       Impact factor: 9.043

5.  Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations.

Authors:  Dana C Crawford; Christopher S Carlson; Mark J Rieder; Dana P Carrington; Qian Yi; Joshua D Smith; Michael A Eberle; Leonid Kruglyak; Deborah A Nickerson
Journal:  Am J Hum Genet       Date:  2004-03-10       Impact factor: 11.025

6.  Incorporating genotyping uncertainty in haplotype inference for single-nucleotide polymorphisms.

Authors:  Hosung Kang; Zhaohui S Qin; Tianhua Niu; Jun S Liu
Journal:  Am J Hum Genet       Date:  2004-02-13       Impact factor: 11.025

7.  HapCompass: a fast cycle basis algorithm for accurate haplotype assembly of sequence data.

Authors:  Derek Aguiar; Sorin Istrail
Journal:  J Comput Biol       Date:  2012-06       Impact factor: 1.479

8.  Genotype-based association mapping of complex diseases: gene-environment interactions with multiple genetic markers and measurement error in environmental exposures.

Authors:  Iryna Lobach; Ruzong Fan; Raymond J Carroll
Journal:  Genet Epidemiol       Date:  2010-12       Impact factor: 2.135

9.  High-throughput haplotype determination over long distances by haplotype fusion PCR and ligation haplotyping.

Authors:  Daniel J Turner; Matthew E Hurles
Journal:  Nat Protoc       Date:  2009       Impact factor: 13.491

Review 10.  Missing data imputation and haplotype phase inference for genome-wide association studies.

Authors:  Sharon R Browning
Journal:  Hum Genet       Date:  2008-10-11       Impact factor: 4.132

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