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

 





June 03, 2016

 

 

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**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](http://www.cell.com/action/showFullText?pii=S0092-8674(16)30421-4&journalCode=CELL). [Read More](http://medicalxpress.com/news/2016-06-high-throughput-sensitive-approach-reveal-real.html).



 

 

 



 

 See also:- [ Faculty News ](/news-type/faculty-news)
- [ 2016 ](/news-year/2016)