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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

211 related items for PubMed ID: 16403792

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  • 2. 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
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  • 3. Genome-wide selection of tag SNPs using multiple-marker correlation.
    Hao K.
    Bioinformatics; 2007 Dec 01; 23(23):3178-84. PubMed ID: 18006555
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  • 4. Inference of missing SNPs and information quantity measurements for haplotype blocks.
    Su SC, Kuo CC, Chen T.
    Bioinformatics; 2005 May 01; 21(9):2001-7. PubMed ID: 15699029
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  • 6. Genome resequencing and genetic variation.
    Stratton M.
    Nat Biotechnol; 2008 Jan 01; 26(1):65-6. PubMed ID: 18183021
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  • 8. Simulating association studies: a data-based resampling method for candidate regions or whole genome scans.
    Wright FA, Huang H, Guan X, Gamiel K, Jeffries C, Barry WT, de Villena FP, Sullivan PF, Wilhelmsen KC, Zou F.
    Bioinformatics; 2007 Oct 01; 23(19):2581-8. PubMed ID: 17785348
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  • 11. A new method for SNP discovery.
    Xu JY, Xu GB, Chen SL.
    Biotechniques; 2009 Mar 01; 46(3):201-8. PubMed ID: 19317663
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  • 13. BNTagger: improved tagging SNP selection using Bayesian networks.
    Lee PH, Shatkay H.
    Bioinformatics; 2006 Jul 15; 22(14):e211-9. PubMed ID: 16873474
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  • 14. Constructing near-perfect phylogenies with multiple homoplasy events.
    Satya RV, Mukherjee A, Alexe G, Parida L, Bhanot G.
    Bioinformatics; 2006 Jul 15; 22(14):e514-22. PubMed ID: 16873515
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  • 18. 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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