7. RECOMB 2003: Berlin, Germany

• Tatsuya Akutsu:
  Efficient extraction of mapping rules of atoms from enzymatic reaction data. 1-8
  
• Vineet Bafna, Nathan Edwards:
  On de novo interpretation of tandem mass spectra for peptide identification. 9-18
  
• Vineet Bafna, Bjarni V. Halldórsson, Russell Schwartz, Andrew G. Clark, Sorin Istrail:
  Haplotypes and informative SNP selection algorithms: don't block out information. 19-27
  
• Yoseph Barash, Gal Elidan, Nir Friedman, Tommy Kaplan:
  Modeling dependencies in protein-DNA binding sites. 28-37
  
• Gill Bejerano:
  Efficient exact value computation and applications to biosequence analysis. 38-47
  
• Amir Ben-Dor, Tzvika Hartman, Benno Schwikowski, Roded Sharan, Zohar Yakhini:
  Towards optimally multiplexed applications of universal DNA tag systems. 48-56
  
• Mathieu Blanchette:
  A comparative analysis method for detecting binding sites in coding regions. 57-66
  
• Jeremy Buhler, Uri Keich, Yanni Sun:
  Designing seeds for similarity search in genomic DNA. 67-75
  
• Benny Chor, Amit Khetan, Sagi Snir:
  Maximum likelihood on four taxa phylogenetic trees: analytic solutions. 76-83
  
• Derek Y. Chiang, Alan M. Moses, Manolis Kamvysselis, Eric S. Lander, Michael B. Eisen:
  Phylogenetically and spatially conserved word pairs associated with gene expression changes in yeasts. 84-93
  
• Andrew G. Clark:
  Haplotype phase inference. 94-94
  
• Minghua Deng, Ting Chen, Fengzhu Sun:
  An integrated probabilistic model for functional prediction of proteins. 95-103
  
• Eleazar Eskin, Eran Halperin, Richard M. Karp:
  Large scale reconstruction of haplotypes from genotype data. 104-113
  
• Maáyan Fishelson, Dan Geiger:
  Optimizing exact genetic linkage computations. 114-121
  
• Áprád Furka:
  Combinatorial synthesis on macroscopic solid support units. 122-122
  
• Aristides Gionis, Heikki Mannila:
  Finding recurrent sources in sequences. 123-130
  
• Gideon Greenspan, Dan Geiger:
  Model-based inference of haplotype block variation. 131-137
  
• David Haussler:
  Computational analysis of the human and other mammalian genomes. 138-138
  
• Andreas Heger, Michael Lappe, Liisa Holm:
  Accurate detection of very sparse sequence motifs. 139-147
  
• Andrew B. Kahng, Ion I. Mandoiu, Pavel A. Pevzner, Sherief Reda, Alexander Zelikovsky:
  Engineering a scalable placement heuristic for DNA probe arrays. 148-156
  
• Manolis Kamvysselis, Nick Patterson, Bruce Birren, Bonnie Berger, Eric S. Lander:
  Whole-genome comparative annotation and regulatory motif discovery in multiple yeast species. 157-16
  
• Balaji Krishnapuram, Lawrence Carin, Alexander J. Hartemink:
  Joint classifier and feature optimization for cancer diagnosis using gene expression data. 167-175
  
• Christopher James Langmead, Anthony K. Yan, Ryan H. Lilien, Lincong Wang, Bruce Randall Donald:
  Large a polynomial-time nuclear vector replacement algorithm for automated NMR resonance assignments. 176-187
  
• Neal Lesh, Michael Mitzenmacher, Sue Whitesides:
  A complete and effective move set for simplified protein folding. 188-195
  
• Arthur M. Lesk:
  Invited: Prediction of protein function. 196-196
  
• Jing Li, Tao Jiang:
  Efficient rule-based haplotyping algorithms for pedigree data. 197-206
  
• Lei Li, Jong Hyun Kim, Michael S. Waterman:
  Haplotype reconstruction from SNP alignment. 207-216
  
• Wentian Li, Ivo Grosse:
  Gene selection criterion for discriminant microarray data analysis based on extreme value distributions. 217-223
  
• Niranjan Nagarajan, Golan Yona:
  A multi-expert system for the automatic detection of protein domains from sequence information. 224-234
  
• Christiane Nüsslein-Volhard:
  Invited. 235-235
  
• Dieter Oesterhelt:
  Biology and bioinformatics of halophilism. 236-236
  
• Itsik Pe'er, Jacques S. Beckmann:
  Resolution of haplotypes and haplotype frequencies from SNP genotypes of pooled samples. 237-246
  
• Pavel A. Pevzner, Glenn Tesler:
  Transforming men into mice: the Nadeau-Taylor chromosomal breakage model revisited. 247-256
  
• Krishna M. Roskin, Mark Diekhans, David Haussler:
  Scoring two-species local alignments to try to statistically separate neutrally evolving from selected DNA segments. 257-266
  
• Fabian Schwarzer, Itay Lotan:
  Approximation of protein structure for fast similarity measures. 267-276
  
• Adam C. Siepel, David Haussler:
  Combining phylogenetic and hidden Markov models in biosequence analysis. 277-286
  
• Terence P. Speed:
  Low-level analyses of microarray data. 287-287
  
• Kari Stefansson:
  Invited. 288-288
  
• Umar Syed, Golan Yona:
  Using a mixture of probabilistic decision trees for direct prediction of protein function. 289-300
  
• Amos Tanay, Ron Shamir:
  Modeling transcription programs: inferring binding site activity and dose-response model optimization. 301-310
  
• Edward N. Trifonov:
  Poetry and prose of the sequences. 311-311
  
• Chen-Hsiang Yeang, Tommi Jaakkola:
  Physical network models and multi-source data integration. 312-321
  
• Gene W. Yeo, Christopher B. Burge:
  Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals. 322-331
  
• Kui Zhang, Fengzhu Sun, Michael S. Waterman, Ting Chen:
  Dynamic programming algorithms for haplotype block partitioning: applications to human chromosome 21 haplotype data. 332-340