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SUMMARY:Describing drug toxicity using functional data analysis and the mo
 del-driven clustering of gene-expression  bio-markers - Dr. Quin Wills Sim
 uGen
DTSTART:20060911T130000Z
DTEND:20060911T140000Z
UID:TALK5292@talks.cam.ac.uk
CONTACT:Danielle Stretch
DESCRIPTION:To predict the toxicity of a newly developed drug cheaply\, qu
 ickly and\naccurately is one of the top concerns for the drug discovery an
 d development\nindustry. It is believed that even minor improvements will 
 save over US$200\nmillion per new drug. The FDA believes that a new prod
 uct development\ntoolkit containing  computer-based predictive models is
  urgently needed.\n\nToxicogenomics tries to understand and predict drug
  toxicity by studying\ngene expression. However\, the state of the art suf
 fers from two very\nimportant setbacks (i) it is not model-driven (ii) it 
 doesn't explicitly\nhelp industry decide if a drug should canned or taken 
 further.\n\nUsing a human liver cell culture model\, SimuGen has demonstra
 ted that with\nthe correct choice of biomarkers\, empiric functional data 
 analysis models\,\nand higher level exploratory analysis such as clusterin
 g (based on the\nmodels)\, it is possible to predict and describe liver to
 xicity with greater\nsensitivity than animal tests. We will work through s
 ome of the interesting\nproblems that needed to be addressed to get this r
 ight.\n\nSimuGen is a company inspired by the MPhil CompBio course -  many
  of the\nanswers come directly from methods students will become familiar 
 with.\n\n 
LOCATION:MR5\, DAMTP
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