National Institutes of Health

Description

The NIH invites applications to use whole genome sequencing at an NHGRI-supported sequencing center to investigate the genetic etiology of structural birth defects, and to further elucidate the genetic contribution to childhood cancers and the genomic contributions to treatment failure for childhood sarcomas.These data will become part of a data resource for the pediatric research community. Information from this activity will be used to help design future activities of the Gabriella Miller Kids First (Kids First) Pediatric Research Program.

Who can apply

• State governments
• County governments
• City or township governments
• Special district governments
• Independent school districts
• Public and State controlled institutions of higher education
• Native American tribal governments (Federally recognized)
• Public housing authorities / Indian housing authorities
• 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
• Small businesses
• Others

Contact

NIH OER Webmaster<br/>FBOWebmaster@OD.NIH.GOV<br/>
FBOWebmaster@OD.NIH.GOV