Genome Sequencing Center for the Gabriella Miller Kids First Pediatric Research Program (U24)
ArchivedNational Institutes of Health
Description
The purpose of this Funding Opportunity Announcement (FOA) is to establish one or two centers that can rapidly generate high quality whole genome sequence and variant data from a large number of human specimens representing two types of pediatric conditions - structural birth defects and childhood cancers. The generated data will become a part of a data resource under The Gabriella Miller Kids First Pediatric Research Program, which will allow researchers to investigate the genetic etiology of structural birth defects, and to further elucidate the genetic contribution to childhood cancers.
Who can apply
- State governments
- County governments
- City or township governments
- Special district governments
- Public and State controlled institutions of higher education
- Native American tribal governments (Federally recognized)
- Native American tribal organizations (other than Federally recognized)
- Nonprofits with 501(c)(3) status (other than higher education)
- Nonprofits without 501(c)(3) status (other than higher education)
- Private institutions of higher education
- For-profit organizations other than small businesses
Contact
eRA Service Desk <br/>Monday to Friday 7 am to 8 pm ET <br/>http://grants.nih.gov/support/ <br/>Phone 1-866-504-9552
GrantsInfo@nih.gov
- PostedJan 13, 2016
- ClosesMar 31, 2016
- Award ceiling$12,600,000
- Program funding$12,600,000
- CFDA93.310
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