Kaitlin Samocha, Ph.D.


Assistant Investigator
Center for Genomic Medicine, Mass General Research Institute
Member of the Faculty of Medicine
Harvard Medical School
A.B. University of Chicago
Ph.D. Harvard University
disease genetics; genomics; rare genetic diseases; selection genetic Our group studies patterns of rare genetic variation in large collections of human genomic data, both from patients and reference population individuals, and designs tools and methods to help interpret that variation. We are focused on moving from studying single variants at a time to understanding how they impact disease in their genomic context.
Publications
Center for Genomic Medicine
Simches Building
185 Cambridge Street
Boston, MA 02114-2790