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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]