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- Multi-Omics for Health and Disease (Multi-Omics)1
- Ethical, Legal and Social Implications (ELSI) Research Program5
- Genomics-Enabled Learning Health Systems (gLHS)2
- Genome Technology Program5
- Impact of Genomic Variation on Function (IGVF) Consortium1
- Clinical Genome (ClinGen) Resource1
- Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium1
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium2
Event
NSIGHT explores the implications, challenges and opportunities associated with the possible use of genomic sequence information during the newborn period.
… associated with the possible use of genomic sequence information during the newborn period. The NSIGHT program … associated with the possible use of genomic sequence information during the newborn period. … NSIGHT explores the … associated with the possible use of genomic sequence information during the newborn period. … Event …
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.
… into this model, health systems can capture genomic information from every patient encounter, generating evidence … to identify and advance approaches for integrating genomic information into existing learning health systems. … The … to identify and advance approaches for integrating genomic information into existing learning health systems. … Research …
News Release
NIH is awarding $5.4 million in first-year funding to establish a new program that supports the integration of genomics into learning health systems. As genomic testing becomes increasingly common, more and more genomic data are available in clinical settings, and learning health systems present an opportunity to translate this evidence quickly and directly into improvements in medical care.
… Network will analyze and improve how genomic information is integrated into patient care. … The National … to identify and advance approaches for integrating genomic information into existing learning health systems. As genomic … testing for hereditary diseases or using genomic information to select which medications a patient is given. …
Event
On February 16, 2023, the National Human Genome Research Institute (NHGRI) held a follow-up working group consultation after the 14th Genomic Medicine meeting, Genomic Medicine XIV: Genomic Learning Healthcare Systems.
… the All of Us Research Program) MD and GC will provide information about local resources available for clinical … MCED in the clinic as an emerging precision medicine technology. We did trial an e consult service in EPIC but … “learning community of practice” listserv to provide information and updates, potentially supplemented with a …
Event
On January 25, 2023, the National Human Genome Research Institute will hold a roundtable on social and behavioral genomics.
… Moderator: Ashley Smart, Massachusetts Institute of Technology Daniel Benjamin, University of California, Los … the public. Follow #NHGRIevents on social media for more information. Agenda Biographies Additional Resources …
Event
NHGRI and NICHD program staff will hold a pre-application interactive Q&A webinar for the Developmental Genotype-Tissue Expression Project funding opportunities and answer questions from prospective applicants.
… have a set of questions that should be asked? The more information that is collected, the better. In the Research … you further clarify what is required? All the information from the BPC regarding tissue samples will be … will be broadly shared without any identifying subject information with the biomedical community.” To recap, tissue …
Event
A 10-part seminar series in 2021 that focuses on the “Bold Predictions for Human Genomics by 2030” that are described in NHGRI’s “Strategic Vision for Improving Human Health at the Forefront of Genomics.”
… analyses of genome sequences and associated phenotypic information for millions of human participants will be … 4:30 p.m. Bold Prediction #6: The regular use of genomic information will have transitioned from boutique to …