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PUBMED FOR HANDHELDS

Journal Abstract Search


267 related items for PubMed ID: 16287933

  • 21. A new method for SNP discovery.
    Xu JY, Xu GB, Chen SL.
    Biotechniques; 2009 Mar; 46(3):201-8. PubMed ID: 19317663
    [Abstract] [Full Text] [Related]

  • 22. SNP mining porcine ESTs with MAVIANT, a novel tool for SNP evaluation and annotation.
    Panitz F, Stengaard H, Hornshøj H, Gorodkin J, Hedegaard J, Cirera S, Thomsen B, Madsen LB, Høj A, Vingborg RK, Zahn B, Wang X, Wang X, Wernersson R, Jørgensen CB, Scheibye-Knudsen K, Arvin T, Lumholdt S, Sawera M, Green T, Nielsen BJ, Havgaard JH, Brunak S, Fredholm M, Bendixen C.
    Bioinformatics; 2007 Jul 01; 23(13):i387-91. PubMed ID: 17646321
    [Abstract] [Full Text] [Related]

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  • 24. SNP discovery using advanced algorithms and neural networks.
    Unneberg P, Strömberg M, Sterky F.
    Bioinformatics; 2005 May 15; 21(10):2528-30. PubMed ID: 15746291
    [Abstract] [Full Text] [Related]

  • 25. High density linkage disequilibrium mapping using models of haplotype block variation.
    Greenspan G, Geiger D.
    Bioinformatics; 2004 Aug 04; 20 Suppl 1():i137-44. PubMed ID: 15262792
    [Abstract] [Full Text] [Related]

  • 26. Genome-wide selection of tag SNPs using multiple-marker correlation.
    Hao K.
    Bioinformatics; 2007 Dec 01; 23(23):3178-84. PubMed ID: 18006555
    [Abstract] [Full Text] [Related]

  • 27. Recovering haplotype structure through recombination and gene conversion.
    Lajoie M, El-Mabrouk N.
    Bioinformatics; 2005 Sep 01; 21 Suppl 2():ii173-9. PubMed ID: 16204098
    [Abstract] [Full Text] [Related]

  • 28. A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.
    Zhang C, Bailey DK, Awad T, Liu G, Xing G, Cao M, Valmeekam V, Retief J, Matsuzaki H, Taub M, Seielstad M, Kennedy GC.
    Bioinformatics; 2006 Sep 01; 22(17):2122-8. PubMed ID: 16845142
    [Abstract] [Full Text] [Related]

  • 29. Revealing the hidden structure of our genome.
    Sharp A.
    Nat Methods; 2006 Jun 01; 3(6):427-8. PubMed ID: 16721375
    [No Abstract] [Full Text] [Related]

  • 30. Haplotypes histories as pathways of recombinations.
    El-Mabrouk N, Labuda D.
    Bioinformatics; 2004 Aug 12; 20(12):1836-41. PubMed ID: 14988100
    [Abstract] [Full Text] [Related]

  • 31. Accounting for genotyping errors in tagging SNP selection.
    Liu W, Yang T, Zhao W, Chase GA.
    Ann Hum Genet; 2007 Jul 12; 71(Pt 4):467-79. PubMed ID: 17346256
    [Abstract] [Full Text] [Related]

  • 32. ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays.
    Rigaill G, Hupé P, Almeida A, La Rosa P, Meyniel JP, Decraene C, Barillot E.
    Bioinformatics; 2008 Mar 15; 24(6):768-74. PubMed ID: 18252739
    [Abstract] [Full Text] [Related]

  • 33. A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.
    Xiao Y, Segal MR, Yang YH, Yeh RF.
    Bioinformatics; 2007 Jun 15; 23(12):1459-67. PubMed ID: 17459966
    [Abstract] [Full Text] [Related]

  • 34. An efficient comprehensive search algorithm for tagSNP selection using linkage disequilibrium criteria.
    Qin ZS, Gopalakrishnan S, Abecasis GR.
    Bioinformatics; 2006 Jan 15; 22(2):220-5. PubMed ID: 16269414
    [Abstract] [Full Text] [Related]

  • 35. A double classification tree search algorithm for index SNP selection.
    Zhang P, Sheng H, Uehara R.
    BMC Bioinformatics; 2004 Jul 06; 5():89. PubMed ID: 15238162
    [Abstract] [Full Text] [Related]

  • 36. CHOISS for selection of single nucleotide polymorphism markers on interval regularity.
    Lee S, Kang C.
    Bioinformatics; 2004 Mar 01; 20(4):581-2. PubMed ID: 14764562
    [Abstract] [Full Text] [Related]

  • 37. PoooL: an efficient method for estimating haplotype frequencies from large DNA pools.
    Zhang H, Yang HC, Yang Y.
    Bioinformatics; 2008 Sep 01; 24(17):1942-8. PubMed ID: 18573795
    [Abstract] [Full Text] [Related]

  • 38. Large scale genotype-phenotype correlation analysis based on phylogenetic trees.
    Habib F, Johnson AD, Bundschuh R, Janies D.
    Bioinformatics; 2007 Apr 01; 23(7):785-8. PubMed ID: 17267431
    [Abstract] [Full Text] [Related]

  • 39. SNP-VISTA: an interactive SNP visualization tool.
    Shah N, Teplitsky MV, Minovitsky S, Pennacchio LA, Hugenholtz P, Hamann B, Dubchak IL.
    BMC Bioinformatics; 2005 Dec 08; 6():292. PubMed ID: 16336665
    [Abstract] [Full Text] [Related]

  • 40. Automated identification of single nucleotide polymorphisms from sequencing data.
    Takahashi M, Matsuda F, Margetic N, Lathrop M.
    Proc IEEE Comput Soc Bioinform Conf; 2002 Dec 08; 1():87-93. PubMed ID: 15838126
    [Abstract] [Full Text] [Related]


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