The National Human Genome Research Institute's 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.
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 for the GSPACs - awarded May 2016:
The currently funded centers are:
More information on the GSPACs, including publications, can be found on the Coordinating Center's website: http://gspac.rutgers.edu/.
Adam Felsenfeld, Ph.D.
Division of Genome Sciences
Posted: September 26, 2018