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Journal Abstract Search
542 related items for PubMed ID: 15588288
21. Pegasys: software for executing and integrating analyses of biological sequences. Shah SP, He DY, Sawkins JN, Druce JC, Quon G, Lett D, Zheng GX, Xu T, Ouellette BF. BMC Bioinformatics; 2004 Apr 19; 5():40. PubMed ID: 15096276 [Abstract] [Full Text] [Related]
22. SynBrowse: a synteny browser for comparative sequence analysis. Pan X, Stein L, Brendel V. Bioinformatics; 2005 Sep 01; 21(17):3461-8. PubMed ID: 15994196 [Abstract] [Full Text] [Related]
23. JUICE: a data management system that facilitates the analysis of large volumes of information in an EST project workflow. Latorre M, Silva H, Saba J, Guziolowski C, Vizoso P, Martinez V, Maldonado J, Morales A, Caroca R, Cambiazo V, Campos-Vargas R, Gonzalez M, Orellana A, Retamales J, Meisel LA. BMC Bioinformatics; 2006 Nov 23; 7():513. PubMed ID: 17123449 [Abstract] [Full Text] [Related]
24. SITEBLAST--rapid and sensitive local alignment of genomic sequences employing motif anchors. Michael M, Dieterich C, Vingron M. Bioinformatics; 2005 May 01; 21(9):2093-4. PubMed ID: 15598827 [Abstract] [Full Text] [Related]
25. ALINE: a WYSIWYG protein-sequence alignment editor for publication-quality alignments. Bond CS, Schüttelkopf AW. Acta Crystallogr D Biol Crystallogr; 2009 May 01; 65(Pt 5):510-2. PubMed ID: 19390156 [Abstract] [Full Text] [Related]
26. 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 [Abstract] [Full Text] [Related]
27. Automatic identification of large collections of protein-coding or rRNA sequences. Arigon AM, Perrière G, Gouy M. Biochimie; 2008 Apr 08; 90(4):609-14. PubMed ID: 17920750 [Abstract] [Full Text] [Related]
29. Multiple alignment of genomic sequences using CHAOS, DIALIGN and ABC. Pöhler D, Werner N, Steinkamp R, Morgenstern B. Nucleic Acids Res; 2005 Jul 01; 33(Web Server issue):W532-4. PubMed ID: 15980528 [Abstract] [Full Text] [Related]
34. A workbench for multiple alignment construction and analysis. Schuler GD, Altschul SF, Lipman DJ. Proteins; 1991 Jul 05; 9(3):180-90. PubMed ID: 2006136 [Abstract] [Full Text] [Related]
35. LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA. Brudno M, Do CB, Cooper GM, Kim MF, Davydov E, NISC Comparative Sequencing Program, Green ED, Sidow A, Batzoglou S. Genome Res; 2003 Apr 05; 13(4):721-31. PubMed ID: 12654723 [Abstract] [Full Text] [Related]
36. webPRANK: a phylogeny-aware multiple sequence aligner with interactive alignment browser. Löytynoja A, Goldman N. BMC Bioinformatics; 2010 Nov 26; 11():579. PubMed ID: 21110866 [Abstract] [Full Text] [Related]
37. OrthoMaM v8: a database of orthologous exons and coding sequences for comparative genomics in mammals. Douzery EJ, Scornavacca C, Romiguier J, Belkhir K, Galtier N, Delsuc F, Ranwez V. Mol Biol Evol; 2014 Jul 26; 31(7):1923-8. PubMed ID: 24723423 [Abstract] [Full Text] [Related]
38. A web tool for comparative genomics: G-compass. Fujii Y, Itoh T, Sakate R, Koyanagi KO, Matsuya A, Habara T, Yamaguchi K, Kaneko Y, Gojobori T, Imanishi T. Gene; 2005 Dec 30; 364():45-52. PubMed ID: 16169162 [Abstract] [Full Text] [Related]
39. SeqVis: visualization of compositional heterogeneity in large alignments of nucleotides. Ho JW, Adams CE, Lew JB, Matthews TJ, Ng CC, Shahabi-Sirjani A, Tan LH, Zhao Y, Easteal S, Wilson SR, Jermiin LS. Bioinformatics; 2006 Sep 01; 22(17):2162-3. PubMed ID: 16766557 [Abstract] [Full Text] [Related]
40. SeqTools: visual tools for manual analysis of sequence alignments. Barson G, Griffiths E. BMC Res Notes; 2016 Jan 22; 9():39. PubMed ID: 26801397 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]