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

187 related items for PubMed ID: 15982637

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.
    Matsuzaki H, Dong S, Loi H, Di X, Liu G, Hubbell E, Law J, Berntsen T, Chadha M, Hui H, Yang G, Kennedy GC, Webster TA, Cawley S, Walsh PS, Jones KW, Fodor SP, Mei R.
    Nat Methods; 2004 Nov; 1(2):109-11. PubMed ID: 15782172
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 5. 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; 1(2):113-7. PubMed ID: 15782173
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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; 21(10):1233-7. PubMed ID: 12960966
    [Abstract] [Full Text] [Related]

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

  • 9. Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
    Patil N, Berno AJ, Hinds DA, Barrett WA, Doshi JM, Hacker CR, Kautzer CR, Lee DH, Marjoribanks C, McDonough DP, Nguyen BT, Norris MC, Sheehan JB, Shen N, Stern D, Stokowski RP, Thomas DJ, Trulson MO, Vyas KR, Frazer KA, Fodor SP, Cox DR.
    Science; 2001 Nov 23; 294(5547):1719-23. PubMed ID: 11721056
    [Abstract] [Full Text] [Related]

  • 10. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.
    Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, Hangaishi A, Kurokawa M, Chiba S, Bailey DK, Kennedy GC, Ogawa S.
    Cancer Res; 2005 Jul 15; 65(14):6071-9. PubMed ID: 16024607
    [Abstract] [Full Text] [Related]

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

  • 12. CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.
    Huang J, Wei W, Chen J, Zhang J, Liu G, Di X, Mei R, Ishikawa S, Aburatani H, Jones KW, Shapero MH.
    BMC Bioinformatics; 2006 Feb 21; 7():83. PubMed ID: 16504045
    [Abstract] [Full Text] [Related]

  • 13. A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide gene dosage effect.
    Agnelli L, Mosca L, Fabris S, Lionetti M, Andronache A, Kwee I, Todoerti K, Verdelli D, Battaglia C, Bertoni F, Deliliers GL, Neri A.
    Genes Chromosomes Cancer; 2009 Jul 21; 48(7):603-14. PubMed ID: 19396863
    [Abstract] [Full Text] [Related]

  • 14. Dynamic variable selection in SNP genotype autocalling from APEX microarray data.
    Podder M, Welch WJ, Zamar RH, Tebbutt SJ.
    BMC Bioinformatics; 2006 Nov 30; 7():521. PubMed ID: 17137502
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Genome-wide analysis of allelic imbalance in prostate cancer using the Affymetrix 50K SNP mapping array.
    Tørring N, Borre M, Sørensen KD, Andersen CL, Wiuf C, Ørntoft TF.
    Br J Cancer; 2007 Feb 12; 96(3):499-506. PubMed ID: 17245344
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.
    Carr J, Bown NP, Case MC, Hall AG, Lunec J, Tweddle DA.
    Cancer Genet Cytogenet; 2007 Jan 15; 172(2):127-38. PubMed ID: 17213021
    [Abstract] [Full Text] [Related]

  • 19. Detecting single-feature polymorphisms using oligonucleotide arrays and robustified projection pursuit.
    Cui X, Xu J, Asghar R, Condamine P, Svensson JT, Wanamaker S, Stein N, Roose M, Close TJ.
    Bioinformatics; 2005 Oct 15; 21(20):3852-8. PubMed ID: 16118260
    [Abstract] [Full Text] [Related]

  • 20. [Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0].
    Ma F, Wu FX, Li N, Liu Q, Yang W, Zhang X, Sun M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 15; 26(3):336-9. PubMed ID: 19504452
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.