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Michael Brudno: [Publications] [Author Rank by year] [Co-authors] [Prefers] [Cites] [Cited by]

Publications of Author

  1. Chuong B. Do, Michael Brudno, Serafim Batzoglou
    PROBCONS: Probabilistic Consistency-Based Multiple Alignment of Amino Acid Sequences. [Citation Graph (0, 0)][DBLP]
    AAAI, 2004, pp:703-708 [Conf]
  2. Michael Brudno, Burkhard Morgenstern
    Fast and Sensitive Alignment of Large Genomic Sequences. [Citation Graph (0, 0)][DBLP]
    CSB, 2002, pp:138-0 [Conf]
  3. Michael Brudno, Sanket Malde, Alexander Poliakov, Chuong B. Do, Olivier Couronne, Inna Dubchak, Serafim Batzoglou
    Glocal alignment: finding rearrangements during alignment. [Citation Graph (0, 0)][DBLP]
    ISMB (Supplement of Bioinformatics), 2003, pp:54-62 [Conf]
  4. Mukund Sundararajan, Michael Brudno, Kerrin Small, Arend Sidow, Serafim Batzoglou
    Chaining Algorithms for Alignment of Draft Sequence. [Citation Graph (0, 0)][DBLP]
    WABI, 2004, pp:326-337 [Conf]
  5. Chris Mayor, Michael Brudno, Jody R. Schwartz, Alexander Poliakov, Edward M. Rubin, Kelly A. Frazer, Lior Pachter, Inna Dubchak
    VISTA : visualizing global DNA sequence alignments of arbitrary length. [Citation Graph (0, 0)][DBLP]
    Bioinformatics, 2000, v:16, n:11, pp:1046-1047 [Journal]
  6. Nameeta Shah, Olivier Couronne, Len A. Pennacchio, Michael Brudno, Serafim Batzoglou, E. Wes Bethel, Edward M. Rubin, Bernd Hamann, Inna Dubchak
    Phylo-VISTA: interactive visualization of multiple DNA sequence alignments. [Citation Graph (0, 0)][DBLP]
    Bioinformatics, 2004, v:20, n:5, pp:636-643 [Journal]
  7. Leila Taher, Oliver Rinner, Saurabh Garg, Alexander Sczyrba, Michael Brudno, Serafim Batzoglou, Burkhard Morgenstern
    AGenDA: homology-based gene prediction. [Citation Graph (0, 0)][DBLP]
    Bioinformatics, 2003, v:19, n:12, pp:1575-1577 [Journal]
  8. Michael Brudno, Michael Chapman, Berthold Göttgens, Serafim Batzoglou, Burkhard Morgenstern
    Fast and sensitive multiple alignment of large genomic sequences. [Citation Graph (0, 0)][DBLP]
    BMC Bioinformatics, 2003, v:4, n:, pp:66- [Journal]
  9. Galina Yu. Kovaleva, Georgii A. Bazykin, Michael Brudno, Mikhail S. Gelfand
    Comparative Genomics of Transcriptional Regulation in Yeasts and its Application to Identification of a Candidate Alpha-isopropylmalate Transporter. [Citation Graph (0, 0)][DBLP]
    J. Bioinformatics and Computational Biology, 2006, v:4, n:5, pp:981-998 [Journal]
  10. Michael Brudno, Rasmus Steinkamp, Burkhard Morgenstern
    The CHAOS/DIALIGN WWW server for multiple alignment of genomic sequences. [Citation Graph (0, 0)][DBLP]
    Nucleic Acids Research, 2004, v:32, n:Web-Server-Issue, pp:41-44 [Journal]
  11. I. Dralyuk, Michael Brudno, Mikhail S. Gelfand, Manfred Zorn, Inna Dubchak
    ASDB: database of alternatively spliced genes. [Citation Graph (0, 0)][DBLP]
    Nucleic Acids Research, 2000, v:28, n:1, pp:296-297 [Journal]
  12. Paul Medvedev, Konstantinos Georgiou, Gene Myers, Michael Brudno
    Computability of Models for Sequence Assembly. [Citation Graph (0, 0)][DBLP]
    WABI, 2007, pp:289-301 [Conf]

  13. A robust framework for detecting structural variations in a genome. [Citation Graph (, )][DBLP]

  14. A mixture model for the evolution of gene expression in non-homogeneous datasets. [Citation Graph (, )][DBLP]

  15. Session Introduction. [Citation Graph (, )][DBLP]

  16. FRESCO: Flexible Alignment with Rectangle Scoring Schemes. [Citation Graph (, )][DBLP]

  17. Ab Initio Whole Genome Shotgun Assembly with Mated Short Reads. [Citation Graph (, )][DBLP]

  18. MoGUL: Detecting Common Insertions and Deletions in a Population. [Citation Graph (, )][DBLP]

  19. Read Mapping Algorithms for Single Molecule Sequencing Data. [Citation Graph (, )][DBLP]

  20. SnowFlock: rapid virtual machine cloning for cloud computing. [Citation Graph (, )][DBLP]

  21. Genome variation discovery with high-throughput sequencing data. [Citation Graph (, )][DBLP]

  22. A report on the 2009 SIG on short read sequencing and algorithms (Short-SIG). [Citation Graph (, )][DBLP]

  23. VARiD: A variation detection framework for color-space and letter-space platforms. [Citation Graph (, )][DBLP]

  24. Savant: genome browser for high-throughput sequencing data. [Citation Graph (, )][DBLP]

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