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- Developmental Genotype-Tissue Expression (dGTEx)1
- Ethical, Legal and Social Implications (ELSI) Research Program2
- Genetic Architecture of Complex Traits1
- Genome Technology Program1
- 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
Join us on Wednesday, May 25, as scholars and scientists answer audience questions and address the complexities surrounding historical and present-day eugenics and scientific racism in the context of existing and developing genetic and genomic screening technologies.
… are many cost-effective, minimal-risk options for prenatal genetic screening and diagnosis for various conditions … Panel discussion: A Historical Discussion on Eugenics and Genetic Testing/Screening Panelists: Rebecca Mueller … relevant to their lived experiences? How do we discuss genetic and genomic variation and its connections to health …
Event
On January 25, 2023, the National Human Genome Research Institute will hold a roundtable on social and behavioral genomics.
… GWAS of educational attainment” by the Social Science Genetic Association Consortium Problems with Using … Lucas J. Matthews Social by Nature by Catherine Bliss Genetic ancestry testing among white nationalists: From identity …
Event
On Tuesday, February 6, 2024, the National Human Genome Research Institute hosted an eConsult webinar to provide an overview of three notice of funding opportunities (RFA-HG-24-001, PAR-24-106 and PAR-24-107). Questions were answered during the webinar.
… is not selected for funding. Can consultants order genetic tests for the patient? No. In an eConsult, the … own patient. If the consultant is needed to order the genetic test, this would be a referral. Can some eConsults … to, address. Can the service use non-physicians, such as genetic counselors, PharmDs, nurses, or PhDs to respond to …
FAQ
On October 10, 2024, NHGRI hosted a pre-application webinar for the Population Genomic Screening in Primary Care NOFOs: RFA-HG-24-021, RFA-HG-24-022, and RFA-HG-24-023. These FAQs contain questions answered during that webinar.
… expected to do data cleaning that links clinical data with genetic data? Yes, in collaboration with the CGs and SeqC. … assigned to the CGs for the clinical data and SeqC for the genetic data. The CC will be responsible for linking the clinical data with the genetic data. Will statistical resources be available …
FAQ
Questions and answers to help applicants responding to the ML/AI Tools to Advance Genomic Translational Research (MAGen) notice of funding opportunities (NOFOs): RFA-HG-24-004 and RFA-HG-24-005.
… enhance the prediction of how individuals with pathogenic genetic variants manifest disease—the goal of this NOFO—but …