These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 19908387)

  • 1. Detecting genome-wide haplotype polymorphism by combined use of Mendelian constraints and local population structure.
    Li X; Chen Y; Li J
    Pac Symp Biocomput; 2010; ():348-58. PubMed ID: 19908387
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficient inference of haplotypes from genotypes on a pedigree.
    Li J; Jiang T
    J Bioinform Comput Biol; 2003 Apr; 1(1):41-69. PubMed ID: 15290781
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Computing the minimum recombinant haplotype configuration from incomplete genotype data on a pedigree by integer linear programming.
    Li J; Jiang T
    J Comput Biol; 2005; 12(6):719-39. PubMed ID: 16108713
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A linear-time algorithm for reconstructing zero-recombinant haplotype configuration on a pedigree.
    Lai EY; Wang WB; Jiang T; Wu KP
    BMC Bioinformatics; 2012; 13 Suppl 17(Suppl 17):S19. PubMed ID: 23281626
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole genome identity-by-descent determination.
    Sabaa H; Cai Z; Wang Y; Goebel R; Moore S; Lin G
    J Bioinform Comput Biol; 2013 Apr; 11(2):1350002. PubMed ID: 23600820
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel algorithm for minimum recombinant haplotyping on pedigrees by zero recombinant block partition.
    Jiang HT; Xu Y; Zhao YZ; Chen GL
    Interdiscip Sci; 2010 Jun; 2(2):185-92. PubMed ID: 20640789
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Error detection in SNP data by considering the likelihood of recombinational history implied by three-site combinations.
    Toleno DM; Morrell PL; Clegg MT
    Bioinformatics; 2007 Jul; 23(14):1807-14. PubMed ID: 17510172
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of recombination events, haplotype reconstruction and imputation of sires using half-sib SNP genotypes.
    Ferdosi MH; Kinghorn BP; van der Werf JH; Gondro C
    Genet Sel Evol; 2014 Feb; 46(1):11. PubMed ID: 24495596
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An almost linear time algorithm for a general haplotype solution on tree pedigrees with no recombination and its extensions.
    Li X; Li J
    J Bioinform Comput Biol; 2009 Jun; 7(3):521-45. PubMed ID: 19507288
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haplotype inference from short sequence reads using a population genealogical history model.
    Zhang J; Wu Y
    Pac Symp Biocomput; 2011; ():288-99. PubMed ID: 21121056
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The effect of haplotype-block definitions on inference of haplotype-block structure and htSNPs selection.
    Ding K; Zhou K; Zhang J; Knight J; Zhang X; Shen Y
    Mol Biol Evol; 2005 Jan; 22(1):148-59. PubMed ID: 15371531
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel method for haplotype clustering and visualization.
    Teo YY; Small KS
    Genet Epidemiol; 2010 Jan; 34(1):34-41. PubMed ID: 19479748
    [TBL] [Abstract][Full Text] [Related]  

  • 13. HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination.
    Zhang K; Sun F; Zhao H
    Bioinformatics; 2005 Jan; 21(1):90-103. PubMed ID: 15231536
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Missing data imputation and haplotype phase inference for genome-wide association studies.
    Browning SR
    Hum Genet; 2008 Dec; 124(5):439-50. PubMed ID: 18850115
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inferring haplotypes from genotypes on a pedigree with mutations, genotyping errors and missing alleles.
    Wang WB; Jiang T
    J Bioinform Comput Biol; 2011 Apr; 9(2):339-65. PubMed ID: 21523936
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multi-SNP haplotype analysis methods for association analysis.
    Stram DO; Seshan VE
    Methods Mol Biol; 2012; 850():423-52. PubMed ID: 22307712
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data.
    Yang WY; Hormozdiari F; Wang Z; He D; Pasaniuc B; Eskin E
    Bioinformatics; 2013 Sep; 29(18):2245-52. PubMed ID: 23825370
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A New Pedigree-Based SNP Haplotype Method for Genomic Polymorphism and Genetic Studies.
    Vadva Z; Larsen CE; Propp BE; Trautwein MR; Alford DR; Alper CA
    Cells; 2019 Aug; 8(8):. PubMed ID: 31387299
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A combined long-range phasing and long haplotype imputation method to impute phase for SNP genotypes.
    Hickey JM; Kinghorn BP; Tier B; Wilson JF; Dunstan N; van der Werf JH
    Genet Sel Evol; 2011 Mar; 43(1):12. PubMed ID: 21388557
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Accurate haplotype inference for multiple linked single-nucleotide polymorphisms using sibship data.
    Liu PY; Lu Y; Deng HW
    Genetics; 2006 Sep; 174(1):499-509. PubMed ID: 16783022
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.