National Institutes of Health Grant: Advancing Understanding of Human Non-Coding Genomic Regions

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The National Institutes of Health is offering a grant to develop innovative computational approaches for interpreting sequence variants in human non-protein-coding genomic regions. This grant aims to integrate various data sets to identify potential variants affecting organismal function and disease risk. Applicants are expected to validate the accuracy of their computational methods using experimental data. Closing date for submissions is May 21, 2015.

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Opportunity ID: 243945

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General Information

Document Type:: Grants Notice
Funding Opportunity Number:: RFA-HG-13-013
Funding Opportunity Title:: Interpreting Variation in Human Non-Coding Genomic Regions Using Computational Approaches and Experimental Assessment (R01)
Opportunity Category:: Discretionary
Opportunity Category Explanation::
Funding Instrument Type::
Category of Funding Activity:: Education
Category Explanation::
Expected Number of Awards::
Assistance Listings Number(s):: 93.172 — Human Genome Research
Cost Sharing or Matching Requirement:: No
Version:: Synopsis 2
Posted Date:: Sep 30, 2013
Last Updated Date:: Jan 07, 2015
Original Closing Date for Applications:: Jan 21, 2015
Current Closing Date for Applications:: May 21, 2015
Archive Date:: Jun 21, 2015
Estimated Total Program Funding::
Award Ceiling:: $500,000
Award Floor:: $

Eligibility

Eligible Applicants:: Special district governments
Additional Information on Eligibility:: Other Eligible Applicants include the following:
Alaska Native and Native Hawaiian Serving Institutions; Asian American Native American Pacific Islander Serving Institutions (AANAPISISs); Eligible Agencies of the Federal Government; Faith-based or Community-based Organizations; Hispanic-serving Institutions; Historically Black Colleges and Universities (HBCUs); Indian/Native American Tribal Governments (Other than Federally Recognized); Non-domestic (non-U.S.) Entities (Foreign Organizations); Regional Organizations; Tribally Controlled Colleges and Universities (TCCUs) ; U.S. Territory or Possession; Non-domestic (non-U.S.) Entities (Foreign Institutions) are eligible to apply.
Non-domestic (non-U.S.) components of U.S. Organizations are eligible to apply.

Foreign components, as defined in the NIH Grants Policy Statement, are allowed.

Additional Information

Agency Name:: National Institutes of Health
Description:: This Funding Opportunity Announcement (FOA) solicits applications to develop highly innovative computational approaches for interpreting sequence variants in the non-protein-coding regions of the human genome. The goal is to develop methods that analyze whole-genome sequence data by integrating data sets, such as ones on genome function, phenotypes, patterns of variation, and other features, to identify or substantially narrow the set of variants that are candidates for affecting organismal function leading to disease risk or other traits. The accuracy of the computational approaches developed should be assessed using experimental data.
Link to Additional Information::
Grantor Contact Information:: If you have difficulty accessing the full announcement electronically, please contact:

Version History

Version Modification Description Updated Date
Synopsis 2 Modified to update the close date field, in accordance with the NIH Guide NOT-HG-15-013. Jan 07, 2015
Synopsis 1

Package Status

Below are CLOSED Opportunity Package(s) no longer available for this Funding Opportunity:

Package No: 1

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Packages

Assistance Listings Competition ID Competition Title Opportunity Package ID Opening Date Closing Date Actions Who Can Apply:
FORMS-C Forms-C PKG00186390 Dec 21, 2013 May 21, 2015 View eRA Commons Help Desk Organization Applicants

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