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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

267 related items for PubMed ID: 16287933

  • 1. 2SNP: scalable phasing based on 2-SNP haplotypes.
    Brinza D, Zelikovsky A.
    Bioinformatics; 2006 Feb 01; 22(3):371-3. PubMed ID: 16287933
    [Abstract] [Full Text] [Related]

  • 2. 2SNP: scalable phasing method for trios and unrelated individuals.
    Brinza D, Zelikovsky A.
    IEEE/ACM Trans Comput Biol Bioinform; 2008 Feb 01; 5(2):313-8. PubMed ID: 18451440
    [Abstract] [Full Text] [Related]

  • 3. Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.
    Di X, Matsuzaki H, Webster TA, Hubbell E, Liu G, Dong S, Bartell D, Huang J, Chiles R, Yang G, Shen MM, Kulp D, Kennedy GC, Mei R, Jones KW, Cawley S.
    Bioinformatics; 2005 May 01; 21(9):1958-63. PubMed ID: 15657097
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. SNP-PHAGE--High throughput SNP discovery pipeline.
    Matukumalli LK, Grefenstette JJ, Hyten DL, Choi IY, Cregan PB, Van Tassell CP.
    BMC Bioinformatics; 2006 Oct 23; 7():468. PubMed ID: 17059604
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Constructing near-perfect phylogenies with multiple homoplasy events.
    Satya RV, Mukherjee A, Alexe G, Parida L, Bhanot G.
    Bioinformatics; 2006 Jul 15; 22(14):e514-22. PubMed ID: 16873515
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. BNTagger: improved tagging SNP selection using Bayesian networks.
    Lee PH, Shatkay H.
    Bioinformatics; 2006 Jul 15; 22(14):e211-9. PubMed ID: 16873474
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Genome resequencing and genetic variation.
    Stratton M.
    Nat Biotechnol; 2008 Jan 15; 26(1):65-6. PubMed ID: 18183021
    [No Abstract] [Full Text] [Related]

  • 18. A highly informative SNP linkage panel for human genetic studies.
    Murray SS, Oliphant A, Shen R, McBride C, Steeke RJ, Shannon SG, Rubano T, Kermani BG, Fan JB, Chee MS, Hansen MS.
    Nat Methods; 2004 Nov 15; 1(2):113-7. PubMed ID: 15782173
    [Abstract] [Full Text] [Related]

  • 19. Haplotype reconstruction from genotype data using Imperfect Phylogeny.
    Halperin E, Eskin E.
    Bioinformatics; 2004 Aug 12; 20(12):1842-9. PubMed ID: 14988101
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.