These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


150 related items for PubMed ID: 15130799

  • 1. FBSA: feature-based sequence alignment technique for very large sequences.
    Bellgard M, Kenworthy W.
    Appl Bioinformatics; 2003; 2(3):145-50. PubMed ID: 15130799
    [Abstract] [Full Text] [Related]

  • 2. DNA sequence analysis linguistic tools: contrast vocabularies, compositional spectra and linguistic complexity.
    Bolshoy A.
    Appl Bioinformatics; 2003; 2(2):103-12. PubMed ID: 15130826
    [Abstract] [Full Text] [Related]

  • 3. Gap mapping: a paradigm for aligning two sequences.
    Bellgard M, Gamble T, Reynolds M, Hunter A, Trifonov E, Taplin R.
    Appl Bioinformatics; 2003; 2(3 Suppl):S31-5. PubMed ID: 15130814
    [Abstract] [Full Text] [Related]

  • 4. Gene identification through large-scale EST sequence processing.
    Lindlöf A.
    Appl Bioinformatics; 2003; 2(3):123-9. PubMed ID: 15130797
    [Abstract] [Full Text] [Related]

  • 5. transAlign: using amino acids to facilitate the multiple alignment of protein-coding DNA sequences.
    Bininda-Emonds OR.
    BMC Bioinformatics; 2005 Jun 22; 6():156. PubMed ID: 15969769
    [Abstract] [Full Text] [Related]

  • 6. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL, Ji L, Li YD.
    Yi Chuan Xue Bao; 2004 May 22; 31(5):431-43. PubMed ID: 15478601
    [Abstract] [Full Text] [Related]

  • 7. MISHIMA--a new method for high speed multiple alignment of nucleotide sequences of bacterial genome scale data.
    Kryukov K, Saitou N.
    BMC Bioinformatics; 2010 Mar 18; 11():142. PubMed ID: 20298584
    [Abstract] [Full Text] [Related]

  • 8. Sigma: multiple alignment of weakly-conserved non-coding DNA sequence.
    Siddharthan R.
    BMC Bioinformatics; 2006 Mar 16; 7():143. PubMed ID: 16542424
    [Abstract] [Full Text] [Related]

  • 9. CGAT: a comparative genome analysis tool for visualizing alignments in the analysis of complex evolutionary changes between closely related genomes.
    Uchiyama I, Higuchi T, Kobayashi I.
    BMC Bioinformatics; 2006 Oct 24; 7():472. PubMed ID: 17062155
    [Abstract] [Full Text] [Related]

  • 10. WindowMasker: window-based masker for sequenced genomes.
    Morgulis A, Gertz EM, Schäffer AA, Agarwala R.
    Bioinformatics; 2006 Jan 15; 22(2):134-41. PubMed ID: 16287941
    [Abstract] [Full Text] [Related]

  • 11. Selection of long oligonucleotides for gene expression microarrays using weighted rank-sum strategy.
    Hu G, Llinás M, Li J, Preiser PR, Bozdech Z.
    BMC Bioinformatics; 2007 Sep 19; 8():350. PubMed ID: 17880708
    [Abstract] [Full Text] [Related]

  • 12. MUSA: a parameter free algorithm for the identification of biologically significant motifs.
    Mendes ND, Casimiro AC, Santos PM, Sá-Correia I, Oliveira AL, Freitas AT.
    Bioinformatics; 2006 Dec 15; 22(24):2996-3002. PubMed ID: 17068086
    [Abstract] [Full Text] [Related]

  • 13. Gene function prediction based on genomic context clustering and discriminative learning: an application to bacteriophages.
    Li J, Halgamuge SK, Kells CI, Tang SL.
    BMC Bioinformatics; 2007 May 22; 8 Suppl 4(Suppl 4):S6. PubMed ID: 17570149
    [Abstract] [Full Text] [Related]

  • 14. Multiple structural alignment and clustering of RNA sequences.
    Torarinsson E, Havgaard JH, Gorodkin J.
    Bioinformatics; 2007 Apr 15; 23(8):926-32. PubMed ID: 17324941
    [Abstract] [Full Text] [Related]

  • 15. A profile-based deterministic sequential Monte Carlo algorithm for motif discovery.
    Liang KC, Wang X, Anastassiou D.
    Bioinformatics; 2008 Jan 01; 24(1):46-55. PubMed ID: 18024972
    [Abstract] [Full Text] [Related]

  • 16. Phylogeny based discovery of regulatory elements.
    Gertz J, Fay JC, Cohen BA.
    BMC Bioinformatics; 2006 May 22; 7():266. PubMed ID: 16716228
    [Abstract] [Full Text] [Related]

  • 17. Discovering and detecting transposable elements in genome sequences.
    Bergman CM, Quesneville H.
    Brief Bioinform; 2007 Nov 22; 8(6):382-92. PubMed ID: 17932080
    [Abstract] [Full Text] [Related]

  • 18. PALMA: mRNA to genome alignments using large margin algorithms.
    Schulze U, Hepp B, Ong CS, Rätsch G.
    Bioinformatics; 2007 Aug 01; 23(15):1892-900. PubMed ID: 17537755
    [Abstract] [Full Text] [Related]

  • 19. A novel feature-based method for whole genome phylogenetic analysis without alignment: application to HEV genotyping and subtyping.
    Liu Z, Meng J, Sun X.
    Biochem Biophys Res Commun; 2008 Apr 04; 368(2):223-30. PubMed ID: 18230342
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 8.