The Genome Sequencing Program Analysis Centers (GSPACs) were funded in 2016 to harmonize, access, and analyze the data produced by the sequencing centers. The GSPACs undertake novel, investigator-initiated computational analyses on GSP data and develop methods to discover variants underlying common, complex, and Mendelian diseases.

Participants

The currently funded centers are:

  1. Harvard University School of Public Health
  2. Vanderbilt University School of Medicine
  3. A cross-institutional center at Icahn School of Medicine at Mount SinaiStanford School of Medicine, and University of California at San Francisco School of Pharmacy

More information on the GSPACs, including publications, can be found on the Coordinating Center's website: http://gspac.rutgers.edu/.

The GSPACs work closely with NHLBI's Trans-omics for Precision Medicine Program to harmonize joint variant calls and analyses, functional annotations, and phenotypic information.

Funding Opportunities

  • RFA-HG-15-026 NHGRI Genome Sequencing Program Analysis Centers (U01) (Expired)
    Expiration Date: Aug 26, 2015

    • NOT-HG-15-030 Notice to Clarify the Number of Applications an Institution Can Submit to RFA-HG-15-026 "NHGRI Genome Sequencing Program Analysis Centers (U01)"

Program Staff

Adam Felsenfeld, Ph.D.
Adam Felsenfeld, Ph.D.
  • Program Director
  • Division of Genome Sciences

Last updated: September 26, 2018