Genome Sequencing Center for the Gabriella Miller Kids First Pediatric Research Program (U24)
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.
General information about this opportunity
Last Known Status
Active
Program Number
RFA-RM-16-001 Federal Agency/Office
Agency: Department of Health and Human ServicesOffice: National Institutes of Health
Type(s) of Assistance Offered
Cooperative Agreement Who is eligible to apply/benefit from this assistance?
Applicant Eligibility
See full announcement for complete details. What is the process for applying and being award this assistance?
Deadlines
03/31/2016 Other Assistance Considerations
Formula and Matching Requirements
This program does not have cost sharing or matching requirements. Who do I contact about this opportunity?
Headquarters Office
eRA Service DeskMonday to Friday 7 am to 8 pm ET
http://grants.nih.gov/support/
Phone 1-866-504-9552
Website Address
http://grants.nih.gov/grants/guide/rfa-files/RFA-RM-16-001.html
E-mail Address
GrantsInfo@nih.gov
Financial Information
Obligations
$12,600,000.00 Range and Average of Financial Assistance
Awards up to $12,600,000.00
