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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

302 related items for PubMed ID: 15782170

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  • 23. Visualization of genomic aberrations using Affymetrix SNP arrays.
    Müller A, Holzmann K, Kestler HA.
    Bioinformatics; 2007 Feb 15; 23(4):496-7. PubMed ID: 17138589
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  • 24. 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
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  • 26. De novo assembly and genomic structural variation analysis with genome sequencer FLX 3K long-tag paired end reads.
    Jarvie T, Harkins T.
    Biotechniques; 2008 May 30; 44(6):829-31. PubMed ID: 18476839
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  • 27. 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
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  • 28. LightTyper platform for high-throughput clinical genotyping.
    Murugesan G, Kottke-Marchant K, Ellis S, Agah R, Tubbs R.
    Expert Rev Mol Diagn; 2005 May 23; 5(3):457-71. PubMed ID: 15934821
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  • 29. LdCompare: rapid computation of single- and multiple-marker r2 and genetic coverage.
    Hao K, Di X, Cawley S.
    Bioinformatics; 2007 Jan 15; 23(2):252-4. PubMed ID: 17148510
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  • 36. Genotyping of single nucleotide polymorphisms by arrayed primer extension.
    Tebbutt SJ.
    Methods Mol Biol; 2007 Jan 15; 382():149-61. PubMed ID: 18220230
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  • 38. 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
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  • 39. Effective algorithms for tag SNP selection.
    Liu TF, Sung WK, Li Y, Liu JJ, Mittal A, Mao PL.
    J Bioinform Comput Biol; 2005 Oct 01; 3(5):1089-106. PubMed ID: 16278949
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