Modeling and testing in high-throughput cancer drug screenings

Feb 13

Thursday, February 13, 2020 - 12:00pm to 1:00pm

Gross Hall, Ahmadieh Family Grand Hall, Room 330

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Presenter

Wesley Tansey, postdoctoral research scientist at Columbia University Medical Center

High-throughput drug screens enable biologists to test hundreds of candidate drugs against thousands of cancer cell lines. The sensitivity of a cell line to a drug is driven by the molecular features of the tumor (e.g. gene mutations and expression). In this talk, I will consider two scientific goals at the forefront of cancer biology: (i) predicting drug response from molecular features, and (ii) discovering gene-drug associations that represent candidates for future drug development. I will present an end-to-end model of cancer drug response that combines hierarchical Bayesian modeling with deep neural networks to learn a flexible function from molecular features to drug response. The model achieves the first goal of state-of-the-art predictive performance, but the black box nature of deep learning makes the model difficult to interpret, presenting a barrier to the second goal of uncovering gene-drug associations. I will use this challenge as motivation for the development of a new method, the holdout randomization test (HRT), for conditional independence testing with black box predictive models. Applying the HRT to the deep probabilistic model of cancer drug response yields more biologically-plausible gene-drug associations than the current analysis technique in biology.

Contact

Currin, Ellen
660-5252
ecurrin@ee.duke.edu