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Program Initiatives

 
REFERENCE EPIGENOME MAPPING CENTERS

This initiative, issued as a cooperative agreement (U01), supports reference epigenome production centers developing reference epigenomes of a variety of human cells. The cell types being mapped are selected by the network of awardees with advice from external scientific experts, and are likely to include human embryonic stem cells, induced pluripotent stem cells, differentiating cells, differentiated cell populations, and human primary cells that are relevant to complex human disease. These epigenomic maps will include information about DNA methylation, histone modifications, and associated non-coding RNAs. Functional correlates of these epigenetic marks, such as gene expression and chromatin accessibility (DNAseI hypersensitivity), will also be measured. The comprehensive data sets comprising this valuable community resource can be used to understand basic biological processes as well as disease mechanisms, provide insights into epigenetic and genetic disease susceptibility, and assist in the identification of potential therapeutic targets. Funding for the Reference Epigenome Mapping Centers began in Fall 2008. More information on this program can be found at http://www.roadmapepigenomics.org/Exit Disclaimer.
 

EPIGENOMICS DATA ANALYSIS AND COORDINATION CENTER (EDACC)

This cooperative agreement (U01) funds the Epigenomics Data Analysis and Coordination Center (EDACC), which provides data analysis and coordination for all of the Reference Epigenome Mapping Centers, as well as imports all other Roadmap Epigenomics Program data generated outside of the mapping centers. In addition, the EDACC is responsible for coordinating with the National Center for Biotechnology Information (NCBI) to develop and implement a data pipeline for transferring and tracking standardized data to NCBI for banking and public utility. The EDACC was originally funded in Fall 2008, and maintains the Human Epigenome Atlas, found at http://www.genboree.org/epigenomeatlas/index.rhtmlExit Disclaimer.

 

TECHNOLOGY DEVELOPMENT IN EPIGENOMICS

This initiative supports technology development in two important areas of epigenetics research. The first area is to develop technologies that will revolutionize epigenetic profiling and/or whole epigenome studies. The second area is to enable in vivo imaging of epigenetic changes in cells, tissues and eventually intact organisms. This initiative was initially launched under two separate RFAs - an R01 (research project) and an R21 (exploratory/developmental project) - both of these were funded in Fall 2008. A second RFA (R01) focused on in vivo imaging of epigenetic changes was funded in Fall 2010.
 

DISCOVERY OF NOVEL EPIGENETIC MARKS IN MAMMALIAN CELLS

The current catalog of known epigenetic marks (as well as proteins that create, remove, and "read"; these marks) is likely incomplete. This initiative supports research aimed at identifying novel epigenetic marks and establishing their function in mammalian cells. It is anticipated that the results of these studies would quickly be translated to global epigenome mapping in human cells (conducted by the Reference Epigenome Mapping Centers). This initiative was launched in Fall 2007 under two separate RFAs - an R01 (research project) and an R21 (exploratory/developmental project), and was funded in Fall 2008.
 

EPIGENOMICS OF HUMAN HEALTH AND DISEASE

This initiative supports research to identify fundamental epigenetic changes or epigenetic mechanisms underlying specific diseases; conditions of development or aging; or response to exposures (physical, chemical, behavioral, and social factors). This initiative was funded as a 50/50 cost share between the NIH Roadmap and specific NIH Institutes, Centers, and Offices. The Roadmap/IC co-funding mechanism fosters multiple IC involvement and ensures easy transition to individual ICs at the end of each funding period. A follow-up RFA (RFA-ES-10-002) was recently released as a multi-institute, Roadmap-affiliated initiative. These awards are expected to be made in Summer, 2011.
 

 

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