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Event
NHGRI workshop seeking scientific perspectives for relating genomic variation to human phenotype.
… strategy to advance our ability to find and characterize genomic variants, the genomic elements in which they reside or that they affect and … … MD … 1750 Rockville Pike … From Genome to Phenotype: Genomic Variation Identification, Association, and Function …
Event
For researchers interested in applying to the Genomic Innovator Award funding opportunity
… Genomic Innovator Award (R35 Clinical Trial Optional)   … 31, 2020 Notice of Pre-Application Webinars for the NHGRI Genomic Innovator Award NOT-HG-20-053 … Funding Opportunities … webinar for researchers interested in applying to the Genomic Innovator Award funding opportunity. Participation in …
News Release
CMG investigators have made significant inroads in discovering genes underlying Mendelian conditions and have uncovered 470 new, previously unknown conditions.
… it was charged with the ambitious task of identifying the genomic underpinnings of as many Mendelian conditions as … in a single gene. So far, researchers have identified the genomic causes for only about half. Individually, a rare … have also made more than 960 discoveries linking specific genomic changes with diseases. These include 375 previously …
Event
On August 15-16, the National Human Genome Research Institute (NHGRI), the National Science Foundation (NSF) and the United States Department of Agriculture (USDA) sponsored a meeting Perspectives in Comparative Genomics and Evolution at the Bethesda North Marriott Hotel & Conference Center in Rockville, Maryland.
… comparative genomics with a focus on commonalities across genomic investigations into humans, model organisms (both …
News Release
NHGRI-funded CSER investigators and colleagues point to need for greater evidence that DNA sequencing helps patients.
… genomics in medicine. CSER investigators have discovered genomic variants - differences in the DNA code - that could … Bethesda, Maryland, for a one-day conference, Integrating Genomic Sequencing into Clinical Care: CSER and Beyond . The … the next 5 to 10 years. To strengthen the case for using genomic sequencing in the clinic, for example, speakers …
Event
On March 1, 2018, over 65 basic research, clinical, and bioinformatic scientists in the genomics community convened for a four-hour web meeting on NHGRI-funded components of the Genome Reference Consortium (GRC).
News Release
The National Institutes of Health (NIH) Genomic Data Sharing Policy includes expectations for how researchers should obtain, share and access genomic data from human and non-human sources. As a leader in genomics, including relevant policy development and implementation, the National Human Genome Research Institute (NHGRI) encourages data sharing practices that go beyond the NIH expectations.
… Ganguly, Ph.D. … The National Institutes of Health (NIH) Genomic Data Sharing Policy includes expectations for how researchers should obtain, share and access genomic data from human and non-human sources. As a leader in … for future research use and broad data sharing of all genomic data derived from human sources, such as specimens …
News Release
NIH-backed African scientists are engaged in a global research endeavor to understand the genetic basis of disease in all populations.
Events
The National Human Genome Research Institute (NHGRI) hosted the Advanced Genomic Technology Development Meeting at Northeastern University in Boston, Massachusetts, on May 29 - 31, 2019.
… Genome Research Institute (NHGRI) hosted the Advanced Genomic Technology Development Meeting at Northeastern … and technical challenges to advancing a broad set of genomic technologies including those for nucleic acid sequencing.  The meeting brought together NHGRI Genomic Technology Program grantees and other scientists and …
News Release
NIH will support research that incorporates DNA sequence information into electronic medical records.
… and Genomics (eMERGE) network is to better understand the genomic basis of disease and to tailor medical care to individual patients based on their genomic differences. … Incorporating Genomics into EMRs The … by identifying the potential medical effects of rare genomic variants (inherited differences in the DNA code) in …