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PUBMED FOR HANDHELDS

Journal Abstract Search


542 related items for PubMed ID: 15588288

  • 1. ABC: software for interactive browsing of genomic multiple sequence alignment data.
    Cooper GM, Singaravelu SA, Sidow A.
    BMC Bioinformatics; 2004 Dec 08; 5():192. PubMed ID: 15588288
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  • 4. PROMPT: a protein mapping and comparison tool.
    Schmidt T, Frishman D.
    BMC Bioinformatics; 2006 Jul 04; 7():331. PubMed ID: 16817977
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  • 5. Combo: a whole genome comparative browser.
    Engels R, Yu T, Burge C, Mesirov JP, DeCaprio D, Galagan JE.
    Bioinformatics; 2006 Jul 15; 22(14):1782-3. PubMed ID: 16709588
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  • 7. The UCSC Genome Browser Database: update 2006.
    Hinrichs AS, Karolchik D, Baertsch R, Barber GP, Bejerano G, Clawson H, Diekhans M, Furey TS, Harte RA, Hsu F, Hillman-Jackson J, Kuhn RM, Pedersen JS, Pohl A, Raney BJ, Rosenbloom KR, Siepel A, Smith KE, Sugnet CW, Sultan-Qurraie A, Thomas DJ, Trumbower H, Weber RJ, Weirauch M, Zweig AS, Haussler D, Kent WJ.
    Nucleic Acids Res; 2006 Jan 01; 34(Database issue):D590-8. PubMed ID: 16381938
    [Abstract] [Full Text] [Related]

  • 8. Look-Align: an interactive web-based multiple sequence alignment viewer with polymorphism analysis support.
    Canaran P, Stein L, Ware D.
    Bioinformatics; 2006 Apr 01; 22(7):885-6. PubMed ID: 16473875
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  • 10. TOPALi: software for automatic identification of recombinant sequences within DNA multiple alignments.
    Milne I, Wright F, Rowe G, Marshall DF, Husmeier D, McGuire G.
    Bioinformatics; 2004 Jul 22; 20(11):1806-7. PubMed ID: 14988107
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  • 11. Phylo-mLogo: an interactive and hierarchical multiple-logo visualization tool for alignment of many sequences.
    Shih AC, Lee DT, Peng CL, Wu YW.
    BMC Bioinformatics; 2007 Feb 24; 8():63. PubMed ID: 17319966
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  • 12. ACT: the Artemis Comparison Tool.
    Carver TJ, Rutherford KM, Berriman M, Rajandream MA, Barrell BG, Parkhill J.
    Bioinformatics; 2005 Aug 15; 21(16):3422-3. PubMed ID: 15976072
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  • 13. GeneTools--application for functional annotation and statistical hypothesis testing.
    Beisvag V, Jünge FK, Bergum H, Jølsum L, Lydersen S, Günther CC, Ramampiaro H, Langaas M, Sandvik AK, Laegreid A.
    BMC Bioinformatics; 2006 Oct 24; 7():470. PubMed ID: 17062145
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  • 14. 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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  • 15. CGHPRO -- a comprehensive data analysis tool for array CGH.
    Chen W, Erdogan F, Ropers HH, Lenzner S, Ullmann R.
    BMC Bioinformatics; 2005 Apr 05; 6():85. PubMed ID: 15807904
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  • 16. 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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  • 17. MANTIS: a phylogenetic framework for multi-species genome comparisons.
    Tzika AC, Helaers R, Van de Peer Y, Milinkovitch MC.
    Bioinformatics; 2008 Jan 15; 24(2):151-7. PubMed ID: 18025004
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  • 18. Genome comparison without alignment using shortest unique substrings.
    Haubold B, Pierstorff N, Möller F, Wiehe T.
    BMC Bioinformatics; 2005 May 23; 6():123. PubMed ID: 15910684
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  • 19. A tool for analyzing and annotating genomic sequences.
    Huang X, Adams MD, Zhou H, Kerlavage AR.
    Genomics; 1997 Nov 15; 46(1):37-45. PubMed ID: 9403056
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  • 20. Processing sequence annotation data using the Lua programming language.
    Ueno Y, Arita M, Kumagai T, Asai K.
    Genome Inform; 2003 Nov 15; 14():154-63. PubMed ID: 15706530
    [Abstract] [Full Text] [Related]


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