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Journal Abstract Search

102 related items for PubMed ID: 17267431

  • 21. Computational identification of candidate loci for recessively inherited mutation using high-throughput SNP arrays.
    Laakso M, Tuupanen S, Karhu A, Lehtonen R, Aaltonen LA, Hautaniemi S.
    Bioinformatics; 2007 Aug 01; 23(15):1952-61. PubMed ID: 17510170
    [Abstract] [Full Text] [Related]

  • 22. 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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  • 23. A conservative test for multiple comparison based on highly correlated test statistics.
    Ninomiya Y, Fujisawa H.
    Biometrics; 2007 Dec 01; 63(4):1135-42. PubMed ID: 17501942
    [Abstract] [Full Text] [Related]

  • 24. SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.
    Reumers J, Maurer-Stroh S, Schymkowitz J, Rousseau F.
    Bioinformatics; 2006 Sep 01; 22(17):2183-5. PubMed ID: 16809394
    [Abstract] [Full Text] [Related]

  • 25. In silico mapping of mouse quantitative trait loci.
    Darvasi A.
    Science; 2001 Dec 21; 294(5551):2423. PubMed ID: 11865449
    [No Abstract] [Full Text] [Related]

  • 26. Marker development for the genetic study of natural variation in Arabidopsis thaliana.
    Nemri A, Neff MM, Burrell M, Jones JD, Studholme DJ.
    Bioinformatics; 2007 Nov 15; 23(22):3108-9. PubMed ID: 18025007
    [Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. Detecting high-order interactions of single nucleotide polymorphisms using genetic programming.
    Nunkesser R, Bernholt T, Schwender H, Ickstadt K, Wegener I.
    Bioinformatics; 2007 Dec 15; 23(24):3280-8. PubMed ID: 18006552
    [Abstract] [Full Text] [Related]

  • 29. In silico mapping of mouse quantitative trait loci.
    Chesler EJ, Rodriguez-Zas SL, Mogil JS.
    Science; 2001 Dec 21; 294(5551):2423. PubMed ID: 11752534
    [No Abstract] [Full Text] [Related]

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  • 33. Definition of arthritis candidate risk genes by combining rat linkage-mapping results with human case-control association data.
    Bäckdahl L, Guo JP, Jagodic M, Becanovic K, Ding B, Olsson T, Lorentzen JC.
    Ann Rheum Dis; 2009 Dec 21; 68(12):1925-32. PubMed ID: 19066175
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  • 34. Consensus generation and variant detection by Celera Assembler.
    Denisov G, Walenz B, Halpern AL, Miller J, Axelrod N, Levy S, Sutton G.
    Bioinformatics; 2008 Apr 15; 24(8):1035-40. PubMed ID: 18321888
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  • 36. Molecular characterization of ENU mouse mutagenesis and archives.
    Sakuraba Y, Sezutsu H, Takahasi KR, Tsuchihashi K, Ichikawa R, Fujimoto N, Kaneko S, Nakai Y, Uchiyama M, Goda N, Motoi R, Ikeda A, Karashima Y, Inoue M, Kaneda H, Masuya H, Minowa O, Noguchi H, Toyoda A, Sakaki Y, Wakana S, Noda T, Shiroishi T, Gondo Y.
    Biochem Biophys Res Commun; 2005 Oct 21; 336(2):609-16. PubMed ID: 16139793
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  • 37. Revealing the hidden structure of our genome.
    Sharp A.
    Nat Methods; 2006 Jun 21; 3(6):427-8. PubMed ID: 16721375
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