Keynote Speakers

Speaker: Eric Jakobsson, Ph.D.
Director, NIGMS Center for Bioinformatics and Computational Biology Chair, NIH Biomedical Information Science and Technology Initiative
Consortum National Institutes of Health

Title: The Role Of Computation In Biomedical Research And Health Care

Abstract

The National Institutes of Health sees that non-trivial computation is critical to every aspect of our mission, from the most basic research to the efficient and effective delivery of health care in all venues. We see the corollary: Inefficiencies, gaps, and flaws in computation are limiting the pace and scope of all aspects of the NIH mission. The Biomedical Information Science and Technology Initiative (BISTI) at the NIH are devoted to implementing our understandings about computation in programs and practices. The core of our immediate programmatic initiative is the creation beginning this year of NIH National Centers for Biomedical Computing around the country, followed by the establishment of a network of collaborating projects. Our ten year goal is for every person involved in the biomedical enterprise---basic researcher, clinical researcher, practitioner, student, teacher, policy maker---to have at their fingertips through their keyboard instant access to all the data sources, analysis tools, modeling tools, visualization tools, and interpretative materials necessary to do their jobs with no inefficiencies in computation or information technology being a rate-limiting step. In twenty years, much of the information retrieval, analysis, and modeling that people will be doing in ten years should be done by intelligent agents, so that people will be able to deal rapidly, effectively, and rigorously with biomedical issues at the highest conceptual level.

Biography of Eric Jakobsson

Eric Jakobsson is a leader in the field of computational biology, an area that joins biology with computer science, engineering, mathematics and physics. His academic degrees are in chemical engineering and physics. While a graduate student in physics, he was drawn to the problem of the physical bases of electrical excitability in nerve. Since 1972 he has been on the faculty at the University of Illinois at Urbana-Champaign, with a primary appointment in Physiology and other appointments in The Beckman Institute for Advanced Science and Technology, Biochemistry, Bioengineering, Biophysics and Computational Biology, the National Center for Supercomputing Applications, and Neuroscience. He has served as the Director of the Center of Biophysics and Computational Biology and the Bioengineering Program. His research interests span many areas of computational biology and include the use of computational technology in education. In May 2003, Jakobsson came to NIH to serve as Director of the Center for Bioinformatics and Computational Biology at the National Institute of General Medical Sciences and the Chair of the NIH Biomedical Information Science and Technology Initiative Consortium. He was the prime drafter of the NIH Bioinformatics and Computational Biology Roadmap, an 8-10 year plan to create an excellent national computational environment for biomedical research. Jakobsson continues to do research at the University of Illinois by weekly commuting.

 


 

Invited Speakers

Speaker: Steven Benner

University of Florida , V. T. and Louise Jackson Distinguished Professor Departments of Chemistry and Anatomy and Cell Biology

Title: Evolutionary Analysis of Protein Sequence Data

Abstract

Computation has been important in molecular studies for some time, but its role is especially critical when the molecules being studied come from living systems. Many of the most common tools used in systems biology, including DNA microarrays and proteomics tools, are noisy to the point of requiring computational tools to have any chance of molecular interpretation. Imaging methods applied in biological systems can generate large volumes of data, often not easily represented by conventional data structures. Data from whole genome sequencing projects do fit into conventional data structures, but the evolutionary analyses that place meaning on these sequences must confront np hard computational tasks. Driving both the information and molecular scientist to confront these problems is a rich set of rewards that success will deliver. These include tools for identifying genes and proteins involved in human disease, the ability to treat patients as individuals through personalized care, and a model for the history of life on Earth, extending from its origins to the modern day. This talk will present examples to illustrate these points.

Biography of Steven Benner

Steven Benner received BS and MS from Yale University in Molecular Biophysics and Biochemistry and PhD from Harvard University in Chemistry. He is Distinguished Professor, Department of Chemistry, University of Florida. He is also Professor of Department of Anatomy and Cell Biology, University of Florida. Before joining Florida, he was Professor of Bio-organic Chemistry, Swiss Federal Institute of Technology. He received several honors and fellowships, and delivered the Carl Sagan Lecture, American Geophysical Union in 2002. His research areas include experimental paleobiochemistry, protein Engineering, combinatorial chemistry, nucleic acid chemistry, nucleic acids enzymology, molecular biology, bioinformatics, planetary biology, phylogenomics, pharmacophylogenomics, and astrobiology.

Speaker: Joyce A. Mitchell

Biomedical and Health Informatics Research and Education Programs and Department of Health Management and Informatics, School of Medicine, University of Missouri

Title: Ontologies in Bioinformatics

Abstract

This talk will start with the basics of ontologies with illustrations of several ontologies that are available in bioinformatics. Examples will be used from (1) the Gene Ontology, used to index gene functional information, (2) the Microarray Gene Expression Data (MGED) Ontologies, used to index the information on microarray experiments, (3) the Clinical Bioinformatics Ontology (CBO), used to create metadata on genetic tests that will be part of electronic medical records, (4) the Medical Subject Headings (MeSH), used to index the scientific literature, and (5) the Unified Medical Language System (UMLS), used to tie together various ontologies to draw inferences from multiple domains. Examples of various ongoing research projects such as the Semantic Web, e-Science, and the author's own collaborative work using ontologies for knowledge discovery should help the audience acquire an understanding of the current areas of research in bioinformatics ontologies.

Biography of Joyce A. Mitchell

Joyce Mitchell is a professor in the School of Medicine, Department of Health Management and Informatics at the University of Missouri-Columbia, with joint appointments in the Division of Medical Genetics and the School of Information Science and Learning Technologies. She received her Ph.D. in population genetics from the University of Wisconsin, Madison. Her postdoctoral research includes both medical information sciences at the University of Missouri and clinical medical genetics at the University of California, San Francisco. She is certified by the American Board of Medical Genetics as a Ph.D. Medical Geneticist. An elected Fellow of the American College of Medical Informatics, she is also a Founding Fellow of the American College of Medical Genetics.

Dr. Mitchell fulfilled several roles for the University of Missouri. While progressing through the professorial ranks, she served as Director of the Medical Information Sciences Group which became the Medical Informatics Group. She further served as Associate Dean for Information Technology of the School of Medicine, and Chief Information Officer for MU Health System. She currently serves as Director of the MU Informatics Institute, with responsibility for graduate education and research programs in both bioinformatics and health informatics. Following a sabbatical at the NLM in 2001-2002, Dr. Mitchell's research is increasingly focused on bioinformatics, including bioinformatics tools in biomedical knowledge discovery, and the incorporation of bioinformatics data into electronic information resources in health care. This research ranges from consumer health website development to the creation of bioinformatics tools for researchers. She is the project co-leader of the NLM's Genetics Home Reference (http://ghr.nlm.nih.gov), a consumer health website dedicated to bringing to the public the health implications and specific genetic data of the Human Genome Project. She is involved with bioinformatics ontology research, including linking ontologies, investigating the use of ontologies in the clinical world, and organizing seminars on biomedical ontologies. Dr. Mitchell has been active in the American College of Medical Informatics (ACMI) and in the American Medical Informatics Association (AMIA), having served on the Board of Directors for both. She was a Chair of the NLM's grant review study section. She served as Chair of the Board of Scientific Counselors (BoSC), a panel that advises on internal NLM research for the Lister Hill National Center for Biomedical Communications.

Speaker: Wen-Hsiung Li

Department of Ecology and Evolution

University of Chicago

Title: Some Topics in Computational Genomics

abstract

Biological (protein interaction and regulatory) networks are current topics in computational genomics. I shall first describe the properties of protein-protein interaction networks. I shall then present a study on the evolution of the yeast protein interaction network. I shall also give a description of regulatory networks. I shall then present a dynamic model of regulatory circuits of yeast genes. This modeling uses a cross-gene identification scheme and the model is shown to give good fit to the expression profiles of yeast genes. It also gives accurate predictions of the expression profiles of genes that have not been used in the construction of the model (in the estimation of the parameters of the model), validating the reliability of the model.

Biography

Wen-Hsiung Li is James D. Watson Professor since 2004 of the Dept of Ecology & Evolution, University of Chicago. He received Ph.D. from Brown University in Applied Math/Genetics, 1972. He was George Beadle Professor 1999-2004 of the Dept of Ecology & Evolution, University of Chicago. He was Professor, 1984-1998, and Betty Wheless Trotter Professor in Medical Sciences, 1996-1998, of the Human Genetics Center, University of Texas Health Science Center-Houston. He started to teach at the University of Texas Health Science Center-Houston since 1973, after one year at Medical Genetics, Univ. of Wisconsin-Madison. Dr. Li received the Balzan Prize 2003 for Genetics and Evolution and Horace Mann Medal 2004. He is Member of the National Academy of Sciences since 2003; Fellow, American Academy of Arts and Sciences 1999; Academician, Academia Sinica, Taiwan 1998; and President, Society for Molecular Biology and Evolution 2000. Among various professional responsibilities, he is Editor, Molecular Phylogenetics and Evolution, 1991 - present; Associate Editor, Journal of Molecular Evolution, 1998 -2004; Associate Editor, Journal of Bioinformatics and Computational Biology, 2003-present; Area Editor (Evolution & Comparative Genomics) Encycl. of Human Genome, Macmillian 1999-present; Editorial Board, Zoological Studies, 1993 -present; Editorial Board, Botanical Bulletin of Academia Sinica, Taiwan, 1993 -present: Scientific Advisory Board, the Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany, 2000-present; Overseers Committee, the Department of Organismic & Evolutionary Biology, Harvard, 2000-present; Academic Advisor, Institute of Zoology, Academia Sinica, Taiwan, 1997 -present; Academic Advisor, Institute of Botany, Academia Sinica, Taiwan, 1997 -present; Academic Advisor, Research Center for Biodiversity, Academia Sinica, Taiwan, 2003 -present; Academic Advisor, Laboratory of Cellular and Molecular Evolution, Kunming Institute of Zoology, The Chinese Academy of Sciences, 1997 -2002; Editorial Board, Mathematical Biosciences, 1990 - 2003; Associate Editor, Theoretical Population Biology, 1981 -1986; Associate Editor, Genetics, 1986 - 1997; Editorial Board, Journal of Molecular Evolution, 1984 - 1997; Editorial Board, Molecular Biology and Evolution, 1983 - 1993; Editor, Gene, 1997 - 2001. His research interests include: Evolutionary Genomics, Molecular Evolution, Bioinformatics and Computational Biology, Population Genetics, Human Genetics. He has published more than 200 papers. His books include: Li, W.-H. Ed. (1977) Stochastic Models in Population Genetics. Dowden, Hutchinson Ross, Stroudsburg, Pa; Li, W.-H. and D. Graur (1991) Fundamentals of Molecular Evolution, Sinauer Associates, Sunderland, Massachusetts; Li, W.-H. (1997) Molecular Evolution, Sinauer Associates, Sunderland, Massachusetts; Graur, D. And W.-H. Li (1999) Fundamentals of Molecular Evolution, 2nd Edition, Sinauer Associates, Sunderland, Massachusetts.

Speaker: Philip E. Bourne

University of California, San Diego, San Diego Supercomputer Center, Burnham Institute, Keck Graduate Institute, and Protein Data Bank

Title: Protein Folds as a Tool in Studying Evolution

Abstract

It is truly remarkable that all of Nature is comprised of a very limited set of parts in the form of protein domain folds - taken here to mean independent and stable folding units. While the exact number remains a point of some conjecture, no one disputes that it is a small number in the 1000s. Some folds are promiscuous, taking part in a variety of functions and some are selective, perhaps having a sole function. At this time we can assign, with reasonable reliability, the number and distribution of domain folds to all fully sequenced genomes (over 150 from the three major kingdoms), achieving 30-60% coverage depending on the complexity of the genome. This presentation will argue that, based on these assignments, we are at a very interesting time in the study of structural bioinformatics, which classifies domain folds, since a useful contribution can be made to the field of molecular evolution. This statement is based on two underlying principles: 1. structure can provide information on distant evolutionary relationships not seem by current methods of sequence analysis; 2. since Nature is comprised of a very limited parts list of protein domain folds, for a species to loose or gain a fold is a major distinguishing event. Using these two principles we will describe our recent efforts in structure-based phylogenetic analysis, including one interpretation of the tree of life.

Biography of Philip E. Bourne

Professor Philip Bourne received his Ph.D. in chemistry from the Flinders University of South Australia in 1980 where he studied the structural and electrophilic effects of substitution on fully saturated caged hydrocarbon molecules. While a post-doctoral fellow at Sheffield University UK he contributed to the understanding of the structural role of the protein ferritin in iron storage. Later as a Senior Research Scientist at Columbia University in New York he proposed mechanisms for the role of caracurines and snake toxins that operate postsynaptically. During the 80's as first the Director of the Cancer Center Computer Facility and later Director of the Medical School Computer Facility at Columbia University he helped establish a tumor registry and various applications and databases in support of patient care. In the early 90's as a Senior Associate of the Howard Hughes Medical Institute he worked on developing high performance hardware and software for computational structural biology. He moved to UCSD in 1995, while bioinformatics was still a bad word, to work on structural bioinformatics. He is currently the Senior Advisor to the Life Sciences at the San Diego Supercomputer Center (SDSC), a Professor in the Department of Pharmacology at UCSD, an Adjunct Professor at the Burnham Institute and the Keck Graduate Institute, Co-Director of the Protein Data Bank (PDB), an elected Fellow of the American Medical Informatics Association and the immediate past President of the International Society for Computational Biology. His current interests are in structural genomics, proteomics, apoptosis, cell signaling, data modeling and scientific visualization. He is the author of over 140 scientific papers and 4 books, one of which sold over 120,000 copies. He has received two UCSD Connect Awards for new inventions in the areas of comparative protein structure analysis and shared visualization. Most recently he was the recipient of the 2002 Sun Microsystems Convergence Award and the 2004 Convocation Medal for career achievement from his graduate university. He has founded two companies, both of which will be successful soon.

Speaker: Susan Baxter

National Center for Genomics Research

Title: Integrated Information Resources for Plant Biology Research Communities

Abstract

Data and information sharing amongst biological research communities promises translation of large scale, collaborative research into improved human health and nutrition. The National Center for Genome Resources (NCGR) has a proven track record in this area and has designed, developed and implemented shared resources for plant biologists, including The Arabidopsis Information Resource (TAIR), The Legume Information System (LIS) and Phytophthora Functional Genomics Database PFGD. Increasingly researchers depend on these resources for comparative and functional genomics projects, requiring databases that allow complex queries. In addition, tools such as the Comparative Map Trait Viewer (CMTV), allow researchers in the field to compare results from their own projects with information available at centralized databases. NCGR is working actively on the design of semantic web services (BioMOBY) and user interfaces to allow researchers to federate information from a variety of information sources.

Biography:

Dr. Susan Baxter, Chief Operating Officer at The National Center for Genome Resources (NCGR), leads and directs software engineering, bioinformatics tool development and information technology for NCGR's discovery platforms, based on data obtained from high-throughput biotechnologies. Prior to joining NCGR, Dr. Baxter was Vice President of Research and Genome Analysis at GeneFormatics, later Cengent Therapeutics, a drug discovery company in San Diego. Her responsibilities included managing programs in both target and lead discovery, along with development of automated protein annotation and analysis pipelines. Previously she was a tenured researcher at the New York State Department of Health's Wadsworth Center, where she used nuclear magnetic resonance spectroscopy to characterize DNA-binding proteins and their complexes. Dr. Baxter received her M.S. and Ph.D. degrees in Chemistry from Northwestern University in Evanston, Illinois. She holds a B.A. degree in Chemistry from the University of Virginia in Charlottesville, Virginia. Following doctoral work, Baxter was an NIH Postdoctoral Fellow at the Institute of Molecular Biology at University of Oregon.

Speaker: Ambuj K. Singh

University of California at Santa Barbara

Title: Current challenges in biological database design

Abstract

Recent spurt in high-throughput techniques has led to phenomenal growth in the quantity and diversity of biological data. There is an immediate need to utilize this data to speed up the progress of biomedical research. Supporting access to such data requires fundamental advances in databases: scalable querying of new data types, use of probabilistic and interpreted data, encoding of complex domain knowledge, and integration of information from multiple data sources. I will broadly discuss the above points and then focus on a couple of applications from bio-image databases and protein interaction networks. These applications illustrate how the individual research thrusts combine to support biological discovery.

Biography of Ambuj K. Singh

Ambuj K. Singh is a professor in the department of computer science at the University of California at Santa Barbara. He received his B.S. from Indian Institute of Technology Kharagpur in 1982, his MS from Iowa State University in 1984, and his PhD from the University of Texas at Austin in 1989. He has been on the faculty at UC Santa Barbara since then. His research interests have been in formal methods, parallel and distributed systems, and databases. More recently, he has been drawn to biological databases, on account of the inherent complexity and novelty, and the reliance on cross-disciplinary knowledge.

Speaker: Weixiong Zhang

Washington University in St. Louis

Title:A steganographic approach to motif finding that combines word counting and statistical modeling

Abstract

It has been a challenge to discover transcription factor (TF) binding motifs (TFBMs), which are short cis-regulatory DNA sequences playing essential roles in transcriptional regulation. We approach the problems of modeling genomic regulatory sequences and discovering TFBMs from a steganographic perspective. In this talk, I will describe an efficient, genome-wide motif finding algorithm, called WordSpy, based on the new perspective. I will discuss the design of WordSpy and its superb performance, comparing many existing algorithms, on recovering the first ten chapters of novel Moby Dick from a stegoscript and discovering all known cell-cycle related TFBM of S. cerevisiae. This is a joint work with Guandong Wang.

Biography of Weixiong Zhang

Dr. Weixiong Zhang is Associate Professor in computer science and genetics at Washington University in Saint Louis. He received his B.S. and M.S. in computer engineering from Tsinghua University, Beijing, China, and his Ph.D. in computer science from UCLA in 1994. From 1994 to 2000, he was Senior Scientist at Information Sciences Institute of USC and research assistant professor at USC. Dr. Zhang's research interests include computational biology (e.g., multiple sequence alignment, RNA folding, targeted gene finding, and gene regulatory networks), artificial intelligence (heuristic search, distributed multiagent systems) and combinatorial optimization (TSP and Boolean satisfiability).

Speaker:Nick Tsinoremas

Informatics Department, The Scripps Research Institute, Jupiter, Florida

Title:Bioinformatics and Lead Discovery Infromatics at Scripps Florida

abstract

The Informatics department at Scripps Florida plays an inherently dual role. On the one hand, it provides support and service to the main research areas of the organization and, on the other, it engages in cutting edge research that leads to a deeper understanding of disease pathways a key component to initiate novel drug discoveries. The research interests of the faculty and research personnel will focus on five main areas: scientific computing, scientific software development, computational biology, drug discovery informatics and chemoinformatics, and data mining and statistical sciences. Since the beginning of the high throughput revolution, research has changed the way in which new biologically active molecules are discovered. Through the widespread adoption of high throughput sequencing, synthesis, and screening, research has become an industrialized process. Automated parallel procedures conducted on a large scale mean that the focus of scientific research has shifted away from the performing of hands-on tasks by scientists to their conceptualizing important correlations for the discovery. Informatics, along with computer sciences and statistics, plays a critical role in the transformation of large-scale discovery research. A number of informatics projects in genomics, proteomics and high through put screening areas will be discussed. Emphasis will be given to Lead Discovery Informatics Infrastructure.

Biography:

NicK Tsinoremas is currently a Senior Director of Informatics at Scripps Florida . His department is responsible for providing informatics and scientific computing support related to Scripps Florida's biomedical research, drug discovery, and technology development programs. Tsinoremas will oversee the development of scientific applications, databases, and data analysis systems that are essential in the drug discovery process, ranging from statistical genetics and data mining to chemo-informatics and sequence-based analysis. Tsinoremas received his B.A. in Chemistry from the University of Athens, Greece and his Ph.D. in Molecular Biology from the University of Leeds, UK. His subsequent postdoctoral work at Texas A & M University focused on light-regulated gene expression and circadian rhythms. Before joining Scripps Florida, he served as director of Computational Genomics and Genomic Discovery at Rosetta/Merck. There he directed the project that combined informatics and computational approaches with gene expression profiling to discover, prioritize, and define drug target genes. Prior to working for Merck/Rosetta, Tsinoremas was the Vice-President of Genomics at DoubleTwist Inc., where he determined the scientific direction of DoubleTwist's bioinformatics applications and databases and was responsible for the creation of Prophecy, the first commercial database annotating all human genes. He also held bioinformatics positions at Incyte Genomics and Progenitor Inc. Tsinoremas' research at Scripps will focus on pattern recognition in sequences, structures and processes, the studying of systems ranging from single protein molecules through complex molecular interactions, and the data analysis, interpretation, and reverse-engineering of complex disease-genomic/genetic interactions in order to enhance our understanding of complex diseases.

Speaker: Louiqa Raschid

Smith School of Business and Institute for Advanced Computer Studies and Center for Bioinformatics and Computational Biology and Department of Computer Science, University of Maryland

Title:Enhancing the Semantics of Links and Paths in Life Science Sources

Abstract

Web-accessible bio-molecular data sources contain data about scientific entities such as genes, sequences, proteins and citations. The sources are diverse in content and richly interconnected to each other. Data integration queries that are critical to scientific exploration explore multiple sources and must traverse both the links and the paths (informally concatenations of links) through these sources. Such navigational queries pose significant challenges because the links are poor with respect to both representation (structure) and meaning. These limitations make it difficult for links to be explored meaningfully when answering queries. In this research, we propose a methodology and tools to assist scientists in exploring and exploiting the knowledge captured in these sources and their interconnections. In order to do so we must accomplish the following: 1. We develop a data model that can represent sources, data objects and the enhanced e-links between data objects. The data model will be augmented with a semantics to compose e-links into meaningful paths, e-paths. 2. We develop a query language and query evaluation engine for scientists to meaningfully explore e-links and e-paths. 3. We develop a methodology to (semi) automatically generate and label links.

Biography:

Louiqa Raschid is Professor of Smith School of Business and Institute for Advanced Computer Studies and Center for Bioinformatics and Computational Biology and Department of Computer Science,University of Maryland. She received her PhD from the University of Florida. At the Robert H. Smith School of Business, she serves also as Leaders for the Digital Economy.


Last Updated: May 30, 2004