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Journal Abstract Search

229 related items for PubMed ID: 18476839

  • 21. HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations.
    Gu S, Pakstis AJ, Kidd KK.
    Bioinformatics; 2005 Oct 15; 21(20):3938-9. PubMed ID: 16131520
    [Abstract] [Full Text] [Related]

  • 22. The metagenome of a biogas-producing microbial community of a production-scale biogas plant fermenter analysed by the 454-pyrosequencing technology.
    Schlüter A, Bekel T, Diaz NN, Dondrup M, Eichenlaub R, Gartemann KH, Krahn I, Krause L, Krömeke H, Kruse O, Mussgnug JH, Neuweger H, Niehaus K, Pühler A, Runte KJ, Szczepanowski R, Tauch A, Tilker A, Viehöver P, Goesmann A.
    J Biotechnol; 2008 Aug 31; 136(1-2):77-90. PubMed ID: 18597880
    [Abstract] [Full Text] [Related]

  • 23. CLUSTAG: hierarchical clustering and graph methods for selecting tag SNPs.
    Ao SI, Yip K, Ng M, Cheung D, Fong PY, Melhado I, Sham PC.
    Bioinformatics; 2005 Apr 15; 21(8):1735-6. PubMed ID: 15585525
    [Abstract] [Full Text] [Related]

  • 24. De novo assembly of the Pseudomonas syringae pv. syringae B728a genome using Illumina/Solexa short sequence reads.
    Farrer RA, Kemen E, Jones JD, Studholme DJ.
    FEMS Microbiol Lett; 2009 Feb 15; 291(1):103-11. PubMed ID: 19077061
    [Abstract] [Full Text] [Related]

  • 25. Towards realistic codon models: among site variability and dependency of synonymous and non-synonymous rates.
    Mayrose I, Doron-Faigenboim A, Bacharach E, Pupko T.
    Bioinformatics; 2007 Jul 01; 23(13):i319-27. PubMed ID: 17646313
    [Abstract] [Full Text] [Related]

  • 26. Whole-genome sequencing and variant discovery in C. elegans.
    Hillier LW, Marth GT, Quinlan AR, Dooling D, Fewell G, Barnett D, Fox P, Glasscock JI, Hickenbotham M, Huang W, Magrini VJ, Richt RJ, Sander SN, Stewart DA, Stromberg M, Tsung EF, Wylie T, Schedl T, Wilson RK, Mardis ER.
    Nat Methods; 2008 Feb 01; 5(2):183-8. PubMed ID: 18204455
    [Abstract] [Full Text] [Related]

  • 27. Genetic diversity and composition of a plasmid metagenome from a wastewater treatment plant.
    Schlüter A, Krause L, Szczepanowski R, Goesmann A, Pühler A.
    J Biotechnol; 2008 Aug 31; 136(1-2):65-76. PubMed ID: 18603322
    [Abstract] [Full Text] [Related]

  • 28. Identifying characteristic scales in the human genome.
    Carpena P, Bernaola-Galván P, Coronado AV, Hackenberg M, Oliver JL.
    Phys Rev E Stat Nonlin Soft Matter Phys; 2007 Mar 31; 75(3 Pt 1):032903. PubMed ID: 17500745
    [Abstract] [Full Text] [Related]

  • 29. Simplified DGS procedure for large-scale genome structural study.
    Jung YC, Xu J, Chen J, Kim Y, Winchester D, Wang SM.
    Biotechniques; 2009 Nov 31; 47(5):969-71. PubMed ID: 20041850
    [Abstract] [Full Text] [Related]

  • 30. SNP detection exploiting multiple sources of redundancy in large EST collections improves validation rates.
    Hayes BJ, Nilsen K, Berg PR, Grindflek E, Lien S.
    Bioinformatics; 2007 Jul 01; 23(13):1692-3. PubMed ID: 17463019
    [Abstract] [Full Text] [Related]

  • 31. RAD paired-end sequencing for local de novo assembly and SNP discovery in non-model organisms.
    Etter PD, Johnson E.
    Methods Mol Biol; 2012 Jul 01; 888():135-51. PubMed ID: 22665280
    [Abstract] [Full Text] [Related]

  • 32. A survey on haplotyping algorithms for tightly linked markers.
    Li J, Jiang T.
    J Bioinform Comput Biol; 2008 Feb 01; 6(1):241-59. PubMed ID: 18324755
    [Abstract] [Full Text] [Related]

  • 33. UCSC genome browser: deep support for molecular biomedical research.
    Mangan ME, Williams JM, Lathe SM, Karolchik D, Lathe WC.
    Biotechnol Annu Rev; 2008 Feb 01; 14():63-108. PubMed ID: 18606360
    [Abstract] [Full Text] [Related]

  • 34. 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]

  • 35. Fast, cost-effective development of species-specific microsatellite markers by genomic sequencing.
    Abdelkrim J, Robertson B, Stanton JA, Gemmell N.
    Biotechniques; 2009 Mar 01; 46(3):185-92. PubMed ID: 19317661
    [Abstract] [Full Text] [Related]

  • 36. Radiation hybrid and linkage mapping of six new type I markers in the horse.
    Bricker SJ, Brault LS, DelValle A, Millon LV, Murray JD, Penedo MC.
    Anim Genet; 2005 Apr 01; 36(2):182-4. PubMed ID: 15771743
    [No Abstract] [Full Text] [Related]

  • 37. Sequencing and assembly of highly heterozygous genome of Vitis vinifera L. cv Pinot Noir: problems and solutions.
    Zharkikh A, Troggio M, Pruss D, Cestaro A, Eldrdge G, Pindo M, Mitchell JT, Vezzulli S, Bhatnagar S, Fontana P, Viola R, Gutin A, Salamini F, Skolnick M, Velasco R.
    J Biotechnol; 2008 Aug 31; 136(1-2):38-43. PubMed ID: 18538432
    [Abstract] [Full Text] [Related]

  • 38. Genomic mutation consequence calculator.
    Major JE.
    Bioinformatics; 2007 Nov 15; 23(22):3091-2. PubMed ID: 17599934
    [Abstract] [Full Text] [Related]

  • 39. Genome sequencing and assembly.
    Grabherr MG, Mauceli E, Ma LJ.
    Methods Mol Biol; 2011 Nov 15; 722():1-9. PubMed ID: 21590409
    [Abstract] [Full Text] [Related]

  • 40. Future tools for association mapping in crop plants.
    Duran C, Eales D, Marshall D, Imelfort M, Stiller J, Berkman PJ, Clark T, McKenzie M, Appleby N, Batley J, Basford K, Edwards D.
    Genome; 2010 Nov 15; 53(11):1017-23. PubMed ID: 21076517
    [Abstract] [Full Text] [Related]

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