Two trends are driving innovation and discovery in biological sciences: technologies that allow holistic surveys of genes, proteins, and metabolites, and the growing realization that analysis and interpretation of the results requires
an understanding of the complex factors that mediate the link between genotype and phenotype. The growing body of biological and biomedical information, driven by an exponential drop in the cost of generating genomic data, provides an outstanding opportunity
for leveraging what we already “know” in a systematic way to understand the problems we are studying. Here, I will provide an overview of some of the methods we are using to investigate the complexities of human phenotypes and to explore how we can use biological
data to uncover the cellular networks and pathways that underlie human disease, building predictive models of those networks that may help to direct therapies.
Speaker bio: