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We are currently looking for a postdoctoral fellow interested in identifying the roles of non-coding variants using whole genome sequencing of patients with rare Mendelian phenotypes. This position is in collaboration with Merck Research Labs. Interested candidates should contact Shamil with a CV and statement of research interests and background.

We have an opportunity for a postdoctoral fellow interested in a computational project on the functional effects of coding variants. Generally, postdoctoral candidates with a strong background in computational biology, population genetics, protein structure or molecular evolution and interested in applications to human genetics are encouraged to contact Shamil.