Pardis Sabeti Joins Research Teams to Build Tool to Help Untangle Genetic Variants

June 3, 2016
Pardis Sabeti

Pardis Sabeti is part of a multi-institutional research team that has demonstrated a tool to help untangle which genetic variants actually create risks for a host of diseases. The team, comprised of scientists from Broad Institute, Harvard University, and Dana-Farber/Boston Children's Cancer and Blood Disorders Center, published their findings in the June 2 issue of Cell.  Read More.

See also: Faculty News, 2016