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PUBMED FOR HANDHELDS

Journal Abstract Search


365 related items for PubMed ID: 12083401

  • 1. SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery.
    Bell PA, Chaturvedi S, Gelfand CA, Huang CY, Kochersperger M, Kopla R, Modica F, Pohl M, Varde S, Zhao R, Zhao X, Boyce-Jacino MT, Yassen A.
    Biotechniques; 2002 Jun; Suppl():70-2, 74, 76-7. PubMed ID: 12083401
    [Abstract] [Full Text] [Related]

  • 2. New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies.
    De La Vega FM, Dailey D, Ziegle J, Williams J, Madden D, Gilbert DA.
    Biotechniques; 2002 Jun; Suppl():48-50, 52, 54. PubMed ID: 12083398
    [Abstract] [Full Text] [Related]

  • 3. Whole genome genotyping technologies on the BeadArray platform.
    Steemers FJ, Gunderson KL.
    Biotechnol J; 2007 Jan; 2(1):41-9. PubMed ID: 17225249
    [Abstract] [Full Text] [Related]

  • 4. BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping.
    Oliphant A, Barker DL, Stuelpnagel JR, Chee MS.
    Biotechniques; 2002 Jun; Suppl():56-8, 60-1. PubMed ID: 12083399
    [Abstract] [Full Text] [Related]

  • 5. Toward genome-wide SNP genotyping.
    Syvänen AC.
    Nat Genet; 2005 Jun; 37 Suppl():S5-10. PubMed ID: 15920530
    [Abstract] [Full Text] [Related]

  • 6. Comparison of PrASE and Pyrosequencing for SNP Genotyping.
    Käller M, Hultin E, Holmberg K, Persson ML, Odeberg J, Lundeberg J, Ahmadian A.
    BMC Genomics; 2006 Nov 16; 7():291. PubMed ID: 17107626
    [Abstract] [Full Text] [Related]

  • 7. Fluorescent microsphere-based readout technology for multiplexed human single nucleotide polymorphism analysis and bacterial identification.
    Ye F, Li MS, Taylor JD, Nguyen Q, Colton HM, Casey WM, Wagner M, Weiner MP, Chen J.
    Hum Mutat; 2001 Apr 16; 17(4):305-16. PubMed ID: 11295829
    [Abstract] [Full Text] [Related]

  • 8. High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise.
    Bray MS, Boerwinkle E, Doris PA.
    Hum Mutat; 2001 Apr 16; 17(4):296-304. PubMed ID: 11295828
    [Abstract] [Full Text] [Related]

  • 9. Genotyping single-nucleotide polymorphisms by minisequencing using tag arrays.
    Lovmar L, Syvänen AC.
    Methods Mol Med; 2005 Apr 16; 114():79-92. PubMed ID: 16156098
    [Abstract] [Full Text] [Related]

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  • 11. A gel-free SNP genotyping method: bioluminometric assay coupled with modified primer extension reactions (BAMPER) directly from double-stranded PCR products.
    Zhou GH, Shirakura H, Kamahori M, Okano K, Nagai K, Kambara H.
    Hum Mutat; 2004 Aug 16; 24(2):155-63. PubMed ID: 15241797
    [Abstract] [Full Text] [Related]

  • 12. SNP genotyping by multiplexed solid-phase amplification and fluorescent minisequencing.
    Shapero MH, Leuther KK, Nguyen A, Scott M, Jones KW.
    Genome Res; 2001 Nov 16; 11(11):1926-34. PubMed ID: 11691857
    [Abstract] [Full Text] [Related]

  • 13. A high-throughput SNP typing system for genome-wide association studies.
    Ohnishi Y, Tanaka T, Ozaki K, Yamada R, Suzuki H, Nakamura Y.
    J Hum Genet; 2001 Nov 16; 46(8):471-7. PubMed ID: 11501945
    [Abstract] [Full Text] [Related]

  • 14. Homogeneous and one-step fluorescent allele-specific PCR for SNP genotyping assays using conjugated polyelectrolytes.
    Duan X, Liu L, Wang S.
    Biosens Bioelectron; 2009 Mar 15; 24(7):2095-9. PubMed ID: 19070477
    [Abstract] [Full Text] [Related]

  • 15. Assessment of two flexible and compatible SNP genotyping platforms: TaqMan SNP Genotyping Assays and the SNPlex Genotyping System.
    De la Vega FM, Lazaruk KD, Rhodes MD, Wenz MH.
    Mutat Res; 2005 Jun 03; 573(1-2):111-35. PubMed ID: 15829242
    [Abstract] [Full Text] [Related]

  • 16. Large-scale genotyping of complex DNA.
    Kennedy GC, Matsuzaki H, Dong S, Liu WM, Huang J, Liu G, Su X, Cao M, Chen W, Zhang J, Liu W, Yang G, Di X, Ryder T, He Z, Surti U, Phillips MS, Boyce-Jacino MT, Fodor SP, Jones KW.
    Nat Biotechnol; 2003 Oct 03; 21(10):1233-7. PubMed ID: 12960966
    [Abstract] [Full Text] [Related]

  • 17. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for genotyping of human platelet-specific antigens.
    Garritsen HS, Fan AX, Bosse N, Hannig H, Kelsch R, Kroll H, Holzgreve W, Zhong XY.
    Transfusion; 2009 Feb 03; 49(2):252-8. PubMed ID: 18980617
    [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 03; 1(2):113-7. PubMed ID: 15782173
    [Abstract] [Full Text] [Related]

  • 19. Detecting imbalanced expression of SNP alleles by minisequencing on microarrays.
    Liljedahl U, Fredriksson M, Dahlgren A, Syvänen AC.
    BMC Biotechnol; 2004 Oct 22; 4():24. PubMed ID: 15500681
    [Abstract] [Full Text] [Related]

  • 20. High-throughput SNP genotyping on universal bead arrays.
    Shen R, Fan JB, Campbell D, Chang W, Chen J, Doucet D, Yeakley J, Bibikova M, Wickham Garcia E, McBride C, Steemers F, Garcia F, Kermani BG, Gunderson K, Oliphant A.
    Mutat Res; 2005 Jun 03; 573(1-2):70-82. PubMed ID: 15829238
    [Abstract] [Full Text] [Related]


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