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- Developmental Genotype-Tissue Expression (dGTEx)1
- Multi-Omics for Health and Disease (Multi-Omics)1
- Ethical, Legal and Social Implications (ELSI) Research Program6
- Genomics-Enabled Learning Health Systems (gLHS)2
- Genetic Architecture of Complex Traits1
- Genome Technology Program5
- Enhancing Opportunities in Computational Genomics and Data Science1
- Human Genome Reference Program (HGRP)2
- Impact of Genomic Variation on Function (IGVF) Consortium3
- Advancing Genomic Medicine Research (AGMR)1
- Encyclopedia of DNA Elements (ENCODE) Project1
- Molecular Phenotypes of Null Alleles in Cells (MorPhiC)1
- Clinical Genome (ClinGen) Resource1
- Genomic Innovator Awards2
- Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium1
- NHGRI Genomic Data Science Analysis, Visualization and Informatics Lab-space (AnVIL)2
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium2
Research Funding
IGNITE enhances genomic medicine by supporting the development of methods for incorporating genomic information into clinical care.
… to find applications in clinical care. The field of "genomic medicine" could potentially improve patient health … The IGNITE demonstration projects will incorporate genomic information into the electronic medical record (EMR) … will contribute to the growing knowledge base of using genomic information in patient care. For more information, …
Research Funding
The Human Genome Reference Program (HGRP) maintains and updates the human genome reference and provides it to the scientific community.
… Reference Diversity UM1HG010971 Active Tool Development Awards Erik Garrison University of Tennessee Health Science … reference U01HG013744 Active Reference Representation Awards Heng Li, Benedict Paten  Dana-Farber Cancer Institute … annotation U01HG010963 Expired Technology Development Awards Karen Miga University of California, Santa Cruz …
Research Funding
The Genomic Variation Program supports large-scale studies of human genetic variation.
… of DNA among individuals are called genetic variation. Genomic variation explains some of the differences among … variants to functional variation and phenotype. The Genomic Variation Program supports large-scale studies of … function and regulation and to clinical effects. … The Genomic Variation Program supports research aimed at: …
Research Funding
The $1,000 Genome Program was a coordinated effort to support the development of technologies to dramatically reduce the cost of DNA sequencing, a move aimed at broadening the applications of genomic information in medical research and health care.
… sequencing, a move aimed at broadening the applications of genomic information in biomedical research and health care. … Technology Development Programs (May 2003 Council) … NIH awards $14.5 million to research groups studying newest DNA … sequencing, a move aimed at broadening the applications of genomic information in medical research and health care. … …
Research Funding
The Genomics-enabled Learning Health System (gLHS) Network aims to identify and advance approaches for integrating genomic information into existing learning health systems.
… Care The VA Genomics Learning Health System: Implementing genomic medicine across diverse veteran communities … System Danville, PA Guthrie Clinic AtlantiCare Making Genomic Medicine Routine in a Rural Healthcare System … of genomics into learning health systems. … NIH awards $27M to establish new network of genomics-enabled …
Research Funding
Bioinformatics and computational biology are cross-cutting areas broadly relevant and fundamental across the entire spectrum of genomics.
… the NIH-funded biomedical data science ecosystem. Read the Genomic Data Science Fact Sheet . See the Draft 2023-2028 NIH … of disease; the implementation and effectiveness of genomic medicine, computational genomics and data science; … and ethical, legal, and social issues related to genomic advances." … The Computational Genomics and Data …
Research Funding
ClinGen will advance genomics in clinical care and improve our understanding of phenotypic and functional effects of genetic variants and their clinical value.
… to disease. As a result, information on only a few genomic variants is used in clinical practice. One factor … are developing standard approaches for sharing genomic and phenotypic data provided by clinicians, … standardize the clinical annotation and interpretation of genomic variants. Working groups are implementing …
Event
Webinar to discuss NHGRI's support of a new Human Genome Reference Program beginning in fiscal year 2020.
Health
GenomeEd is a free repository of high-quality genomics educational resources for group instruction or self-directed learning by healthcare professionals and educators.
Event
NHGRI meeting focused on research that rapidly advances best practices for the implementation of genomic sequence data into clinical care.
… to develop best practices for the implementation of genomic sequence data into clinical care, as well as research … biorepositories with electronic medical record systems for genomic discovery and genomic medicine implementation research. … Hyatt Bethesda …