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Journal Abstract Search

349 related items for PubMed ID: 19514837

  • 21. Frequency Finder: a multi-source web application for collection of public allele frequencies of SNP markers.
    Nguyen TH, Liu C, Gershon ES, McMahon FJ.
    Bioinformatics; 2004 Feb 12; 20(3):439-43. PubMed ID: 14960477
    [Abstract] [Full Text] [Related]

  • 22. SEAN: SNP prediction and display program utilizing EST sequence clusters.
    Huntley D, Baldo A, Johri S, Sergot M.
    Bioinformatics; 2006 Feb 15; 22(4):495-6. PubMed ID: 16357032
    [Abstract] [Full Text] [Related]

  • 23. Restriction enzyme mining for SNPs in genomes.
    Chuang LY, Yang CH, Tsui KH, Cheng YH, Chang PL, Wen CH, Chang HW.
    Anticancer Res; 2008 Feb 15; 28(4A):2001-7. PubMed ID: 18649739
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  • 24. Single nucleotide polymorphism discovery in barley using autoSNPdb.
    Duran C, Appleby N, Vardy M, Imelfort M, Edwards D, Batley J.
    Plant Biotechnol J; 2009 May 15; 7(4):326-33. PubMed ID: 19386041
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  • 25. MultiPipMaker: comparative alignment server for multiple DNA sequences.
    Elnitski L, Riemer C, Burhans R, Hardison R, Miller W.
    Curr Protoc Bioinformatics; 2005 Apr 15; Chapter 10():Unit10.4. PubMed ID: 18428743
    [Abstract] [Full Text] [Related]

  • 26. SNPP: automating large-scale SNP genotype data management.
    Zhao LJ, Li MX, Guo YF, Xu FH, Li JL, Deng HW.
    Bioinformatics; 2005 Jan 15; 21(2):266-8. PubMed ID: 15377503
    [Abstract] [Full Text] [Related]

  • 27. PineSAP--sequence alignment and SNP identification pipeline.
    Wegrzyn JL, Lee JM, Liechty J, Neale DB.
    Bioinformatics; 2009 Oct 01; 25(19):2609-10. PubMed ID: 19667082
    [Abstract] [Full Text] [Related]

  • 28. LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.
    Karchin R, Diekhans M, Kelly L, Thomas DJ, Pieper U, Eswar N, Haussler D, Sali A.
    Bioinformatics; 2005 Jun 15; 21(12):2814-20. PubMed ID: 15827081
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  • 30. 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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  • 33. SNP-VISTA: an interactive SNP visualization tool.
    Shah N, Teplitsky MV, Minovitsky S, Pennacchio LA, Hugenholtz P, Hamann B, Dubchak IL.
    BMC Bioinformatics; 2005 Dec 08; 6():292. PubMed ID: 16336665
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  • 36. Coverage-based consensus calling (CbCC) of short sequence reads and comparison of CbCC results to identify SNPs in chickpea (Cicer arietinum; Fabaceae), a crop species without a reference genome.
    Azam S, Thakur V, Ruperao P, Shah T, Balaji J, Amindala B, Farmer AD, Studholme DJ, May GD, Edwards D, Jones JD, Varshney RK.
    Am J Bot; 2012 Feb 08; 99(2):186-92. PubMed ID: 22301893
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  • 38. 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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