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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

129 related items for PubMed ID: 15927052

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  • 2. Rapid identification of single nucleotide substitutions using SeqDoC.
    Crowe ML.
    Methods Mol Biol; 2007; 396():345-57. PubMed ID: 18025703
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  • 3. 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
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  • 6. 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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  • 7. 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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  • 10. MSQT for choosing SNP assays from multiple DNA alignments.
    Warthmann N, Fitz J, Weigel D.
    Bioinformatics; 2007 Oct 15; 23(20):2784-7. PubMed ID: 17785349
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  • 13. OligoFaktory: a visual tool for interactive oligonucleotide design.
    Schretter C, Milinkovitch MC.
    Bioinformatics; 2006 Jan 01; 22(1):115-6. PubMed ID: 16239305
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  • 14. Web-based primer design software for genome-scale genotyping by pyrosequencing.
    Ringquist S, Pecoraro C, Lu Y, Styche A, Rudert WA, Benos PV, Trucco M.
    Methods Mol Biol; 2007 Jan 01; 373():25-38. PubMed ID: 17185755
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  • 15. IntegratedMap: a Web interface for integrating genetic map data.
    Yang H, Wang H, Gingle AR.
    Bioinformatics; 2005 May 01; 21(9):2126-7. PubMed ID: 15657101
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  • 16. MBEToolbox: a MATLAB toolbox for sequence data analysis in molecular biology and evolution.
    Cai JJ, Smith DK, Xia X, Yuen KY.
    BMC Bioinformatics; 2005 Mar 22; 6():64. PubMed ID: 15780146
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  • 17. GATA: a graphic alignment tool for comparative sequence analysis.
    Nix DA, Eisen MB.
    BMC Bioinformatics; 2005 Jan 17; 6():9. PubMed ID: 15655071
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  • 20. Random mutagenesis-PCR to introduce alterations into defined DNA sequences for validation of SNP and mutation detection methods.
    Nickerson ML, Warren MB, Zbar B, Schmidt LS.
    Hum Mutat; 2001 Mar 17; 17(3):210-9. PubMed ID: 11241843
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