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Friday, September 15, 1:30-3:30 p.m.: Computational Biology
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Computational Biology Overview Talk (1:30-2:00)
Dannie Durand
After a whirlwind review of high school biology, we will discuss the origins of
computational biology and how innovation in biotechnology drives research in
this field. Current research areas in computational biology will be
surveyed with a focus on challenging computer science problems in theory,
systems and AI that arise in computational biology research.
Towards a Systematics for Protein Subcellular Location:
Computer Vision and Automated Learning (2:00-2:30)
Bob Murphy
Determination of the functions of all expressed proteins represents one of
the major upcoming challenges in computational molecular biology. Since
subcellular location plays a crucial role in protein function, the
availability of systems that can predict location from sequence or
high-throughput systems that determine location experimentally will be
essential to the full characterization of expressed proteins. The
development of prediction systems is currently hindered by an absence of
training data that adequately captures the complexity of protein
localization patterns. What is needed is a systematics for the subcellular
locations of proteins. Our group is working on the quantitative
description of protein localization patterns using numerical features and
the use of these features to develop classifiers that can recognize all
major subcellular structures in fluorescence microscope images. Such
classifiers provide a valuable tool for experiments aimed at determining
the subcellular distributions of all expressed proteins. A key conclusion
is that, at least in certain cases, these automated approaches are better
able to distinguish similar protein localization patterns than human
observers. We are also working on systems for inferring protein location
from on-line sources (such as full-text journals) that may disagree or be
subject to error.
Computational Analysis of Vertebrate Genome Evolution (2:30-3:00)
Dannie Durand
Yeast, a simple, single celled organism, has roughly 6000 genes while humans
have 50,000 - 100,000 genes. Yeast can make bread rise. Human beings have
invented the atom bomb and painted the Mona Lisa. How did this
order-of-magnitude increase in gene number arise and how did it lead to the
functional complexity we see in modern vertebrates? Massive gene duplication,
ranging from chromosomal segments to the entire genome, is believed to have
played a crucial role in early vertebrate evolution. In the past, these
processes have been poorly understood, but it is now possible to study these
questions due to the recent availability of huge genomic data sets. In this
talk, I will describe a computational approach to studying vertebrate genome
evolution by exploiting the growing availability of diverse biological data via
the World Wide Web, with an emphasis on the computer science research questions
that arise in this work.
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