DNA regulatory elements in the human genome harbor thousands of genetic risk variants for common diseases and could reveal targets for therapeutics that aim to precisely tune cellular functions — if only we could map the complex regulatory wiring that connects 2 million regulatory elements with 21,000 genes in thousands of cell types in the human body. We combine experimental and computational genomics, biochemistry, molecular biology, and human genetics to assemble regulatory maps of the human genome and uncover biological mechanisms of disease.

We are hiring for positions at Stanford University and at the Broad Institute.

We gratefully acknowledge support from:
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