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4:30 – 6:00 PM
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Welcome reception and introductions (light dinner provided)
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6:00 – 6:15 PM
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Welcome from Peder Jungck, Founder, CloudShield
Brief introduction to workshop, John R. Jungck, PI, BEDROCK
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6:15 – 7:15 PM
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Dr.
Aviv Bergman, Stanford University
Center
for Computational Genetics and Biological Modeling
"Gould's punctuation verses Waddington's
canalization:
A look at micro and macro evolutionary processes"
Despite abundant genetic variation and diverse
environmental conditions phenotypic variation is generally low within
a species. Waddington termed the buffering of developmental processes
against genetic and environmental variation canalization. Gould
emphasized rapid transitions in form and function as an important
factor in the evolutionary record. This talk will use these two
contexts to discuss micro and macro evolutionary mechanisms that
extend basic notions of Darwinian selection.
Dr. Bergman is the co-director of the Center for
Computational Genetics and Biological Modeling at Stanford University.
The research agenda for the center involves interdisciplinary research
into quantitative problems of biology that can be attacked using
a combination of computational and mathematical tools. Article
featuring Dr. Bergman in the Stanford Report.
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7:15 – 7:30 PM
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Break |
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7:15 – 9:00 PM
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Bioinformatics Problem Solving Session #1
Exploring HIV change within and between patients
Drawing biologically meaningful inferences from molecular data -
forensics cases
Sam Donovan, Director, BEDROCK
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9:00 – 9:45 AM
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Overview of The BioQUEST Curriculum Consortium and The BEDROCK
Project
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9:45 – 10:15 AM
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Introduction
to web projects & databases
Amanda Everse, Administrator, BioQUEST web site |
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10:15 – 10:30 AM
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Break
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10:30 – 11:30 AM
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Bioinformatics Problem Solving Session #2
Mapping Multiple Sequence Alignments onto Structures with Protein
Explorer
Tia Johnson, Director of Collaboratories, BEDROCK and Sam Donovan
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11:30 – 1:15 PM
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Lunch and group work
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1:15 – 2:30 PM
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Toward a Theoretical Basis for Bioinformatics: Genetic Codes as
Codes
John R. Jungck
Bioinformatics has largely been developed upon an empirical basis
of statistical patterns; I believe that coding and information theoretical
perspectives along with evolution and biophysics may help us develop
a more theoretically grounded bioinformatics. Mathematical properties
of genetic codes will be demonstrated with respect to their efficiencies,
rates of transmission, detectability and correctability and of errors,
symmetries, and origins by employing coding theory (Baudot codes,
Gray codes, Hamming codes, Huffman Codes (Fractals and Power Laws),
comma free codes, etc.), algorithmic complexity, abstract algebra,
graph theory, combinatorics, information theory, and phylogenetic
systematics of sequences. Genetic codes become much more understandable
and elegant to biologists when they are not considered as mere ciphers,
but are instead understood from three perspectives: codes per se,
physical chemical interactions, and evolutionary selective pressures.
In addition, I will illustrate some of the alternative distance
metrics based upon different mathematical representations of genetic
codes which have utility in genomic data base searching (comparative
sequence analyses) and considerations of different evolutionary
mechanisms.
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2:30 – 2:45 PM
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Break
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2:45 – 3:45 PM
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Bioinformatics Problem Solving Session #3
Studying One Cell with Three Genomes
Sam Donovan, John R. Jungck, Tia Johnson, and Stephen Everse
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3:45 – 4:30 PM
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Group work and
poster preparation |
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4:30 – 5:30 PM
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Social hour
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5:30 PM
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Supper on your own
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8:00 AM
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Facilities open |
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9:00 – 9:45 AM
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Group progress reports using mini-posters
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9:45 – 10:15 AM
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Collaboratories:
Models and Metaphors for Online Collaboration
Tia Johnson |
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10: 15 – 10:30 AM
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Break
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10:30 – 11:30 PM
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Bioinformatics Problem Solving Session #4
RNA
John R. Jungck and Tia Johnson
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11:30 – 1:15 PM
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Lunch and group work and discussions
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1:15 – 2:45 PM
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Dr.
Stephen J. Everse, Department of Biochemistry
College of Medicine, University of Vermont
"Transferrin: Not your average protein"
Transferrins (TF) are a large family of iron binding
proteins. There roles, however, appear to be quite diverse. Serum
TF is the main iron transporter found in the plasma, whereas the
function of lactoferrin (found in milk & other secretions) remains
a mystery. The biological role of ovotransferrin (found in egg whites)
appears to be one of protection. Our goal today will be to look
at the structural similarities and differences to explore their
functionally different roles.
Dr. Everse received his Ph.D. in Chemistry from
the University of California, San Diego in 1995. His postdoctoral
work at UCSD focused on obtaining a structural understanding of
the fibrinogen molecule. His work resulted in the X-ray crystallographic
structures of the fibrinogen fragment D and the fibrin fragment
double-D. He joined the Biochemistry department in the Fall of 1998
as part of the HHMI structural biology initiative at UVM.
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2:45 – 3:00 PM
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Break
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3:00 – 4:30 PM
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Bioinformatics
Problem Solving Session #5
Transferrins: A case study in working with protein families
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5:30 PM
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For those who are interested, we can have supper as a group.
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8:00 AM
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Facilities open |
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Short reports on group projects and next
steps |
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9:00 – 9:20 AM
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Group A |
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9:20 – 9:40 AM
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Group B |
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9:40 – 10:00 AM
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Group C |
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10:00 – 10:20 AM
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Group D |
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10:20 – 10:30 AM
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Break
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10:30 – 12 PM
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- Sharing information about personal projects and courses
- How to contribute and stay involved
- Distribute additional papers and CDs
- Feedback and wrap-up
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For more
information please contact Sam Donovan
or Sue Risseeuw (608/363-2012).
Sponsored
by a grant from the National Science Foundation (DUE/CCLI-ND), the BioQUEST
Curriculum Consortium, and assisted by CloudShield Technologies, Inc.
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