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Figuring Out Life:
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Organizer |
Speakers |
Overview |
This symposium aims to explore the twilight zone between mathematics and biology. The true complexity of biological organisms is only beginning to unfold; in living systems, a collection of properties emerges at each level of organization and in order to cope with the diversity at every scale of spatial and temporal organization, fundamental conceptual advances and interdisciplinary collaborations are inevitable. A thousand or so complete genome sequences are available and we are left with incredible puzzles to solve. Domain expertise is essential, but a powerful approach is to combine reductionist approaches with a holistic understanding. This is where mathematics and computational biology are an integral part of biological research.
Throughout the history mathematics has brought powerful insight in understanding the workings of biological systems. Perhaps the most well known example is the Hardy-Weinberg equilibrium in population genetics, which Hardy and Weinberg devised back in 1908. A more recent example is Kimura’s diffusion equation for gene frequencies in 1994. Mathematics has left many more deep footprints in biological research than is generally realized. For example, Markov models (Markov, 1906) are ubiquitously used in the post-genomics era of today and the list can be made long: age structure of stable populations (Euler, 1760), analysis of variance (Fisher, 1950), dynamics of interacting species (Lotka, 1925; Volterra, 1931), traveling waves in genetics (Fisher, 1937; Kolmogorov et al. 1937), distribution of bacterial mutation rates (Luria and Delbruck, 1943), morphogenesis (Turing, 1952), graph theory and genetic structure (Benzer, 1959), formula for haplotype frequencies (Ewens, 1972) and population coalescence (Kingman, 1982). The list is a mere example and can be made much longer. This interdisciplinary workshop represents a unique opportunity to further explore the twilight zone between mathematics and biology in the post-genomics era. Let’s keep the list growing even longer!
Venue |
Schedule |
Day 1 - Monday, 28 Nov 2005 | |
09:00am - 09:50am |
Registration |
09:50am - 10:00am |
Welcome and Opening Remarks |
10:00am - 10:45am |
Enhancing the recognition
of gene function transfer from model organisms by
considering different levels of conservation of
co-regulation |
10:45am - 11:15am |
--- Coffee Break --- |
11:15am - 12:00nn |
Understanding function using
in silico and experimental structural information |
12:00nn - 12:45pm |
Eukaryotic gene expression: the function of actin and
actin-associated proteins in transcription |
12:45pm - 02:45pm |
--- Lunch break --- |
02:45pm - 03:30pm |
Protein function
prediction from protein interactions |
03:30pm - 04:15pm |
Bioinformatics workflow integration for biomanufacturing
and biosurveillance |
04:15pm - 04:45pm |
--- Coffee Break --- |
04:45pm - 05:30pm |
Cryo-electron tomography
of individual protein molecules |
End of Day 1 |
Day 2 - Tuesday, 29 Nov 2005 | |
09:00am - 09:45am |
Are
complex methods helpful in mapping complex traits (Keynote lecture) |
09:45am - 10:30am |
Size-dependent Pareto-like distributions in genomics,
proteomics and molecular evolution |
10:30am - 11:00am |
--- Coffee Break --- |
11:00am - 11:45am |
Comparative
genomics of two cyprinid species |
11:45am - 12:30pm |
Solvation in proteins:
insights from atomistic simulations |
12:30pm - 02:30pm |
--- Lunch break --- |
02:30pm - 03:15pm |
Inhibition of bacterial
genes using expressed RNA and cell-permeable antisense
agents |
03:15pm - 04:00pm |
Filling
in the GAPs for cell dynamics control |
04:00pm - 04:30pm |
--- Coffee Break --- |
04:30pm - 05:15pm |
Transcriptional targets of STAST5b in liver |
05:15pm - 05:30pm |
Closing Remarks |
End of Symposium |
Registration |
Contacts |