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| Title: | What Can We Do With A Multitude Of Genome Sequences? |
| Authors: | Tompa, Martin University of Washington |
| Subjects : | DNA sequences Functional portions of the human genome Phylogenetic footprinting Sequence alignment |
| Issue Date: | 6-Feb-2008 |
| Publisher: | Georgia Institute of Technology |
| Abstract: | There are currently 575 bacterial species and 28 vertebrate species, ranging from primates to fishes, for which we know (nearly) their entire DNA sequences. These number will continue to increase rapidly over the next few years. Comparing these genome sequences has emerged as one of the most important areas of computational biology. For example, one way to predict functional portions of the human genome is to search among related genomes for sequences that appear to be remarkably similar due to selective pressure. I will discuss and demonstrate some of the methods and tools for such an approach, as well as some of the challenges and unsolved problems. This talk will be self-contained: no knowledge of biology beyond what you have heard in the news will be assumed. |
| Description: | Professor Martin Tompa of the University of Washington presented a lecture at 12 noon on February 6, 2008 in the Klaus building room 1116E on the Georgia Tech campus |
| URI: | http://hdl.handle.net/1853/20067 |
| Appears in Collections: | Computational Science and Engineering Distinguished Lecture Series
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