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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
On March 5-6, 2019, the Genomic Medicine Working Group hosted the Genomics in Health and Wellness Meeting in Bethesda, Maryland.
… Lunch 12:30 - 12:55 p.m. Non-healthcare employer offering genetic testing Jane Gilbert (Teachers' Retirement System of … opportunities and potential projects to deploy genetic tests and a genetics-based testing program within …
Research Funding
Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium will work together to develop and implement approaches to integrating extant genotype and phenotype data for the purpose of conducting and disseminating Consortium-wide PRS analyses.
… and phenotype data (source and harmonized) and summary statistics from the studies and consortia proposed by the …
Research Funding
A list of current and previous Centers of Excellence in Genomic Science (CEGS) grant awards.
… perturbations. However, genome sequencing and clinical genetic testing have far outpaced our ability to understand … an array of technologies to map the effects of genetic variants on molecular and cellular phenotypes, and … and Technology, Health Disparities, Phenotyping, and Statistics. PUBLIC HEALTH RELEVANCE: It is imperative to …
News Release
Stomach cancers fall into four distinct molecular subtypes researchers with The Cancer Genome Atlas Network have found.
Research Funding
The E​MERGE Network develops, disseminates and applies approaches to research that combine biorepositories with electronic medical record systems.​
… researchers with a wide range of expertise in genomics, statistics, ethics, informatics, and clinical medicine from … address this challenge, research that combines patients’ genetic and genomic information with complete longitudinal … contain such longitudinal records, but they typically lack genetic information and store data that is sometimes …
Research Funding
​CSER is rapidly advancing the knowledge necessary to develop best practices for implementating genomic sequence data into clinical care. ​
… Clinical sequencing across communities in the Deep South Genetic disorders in newborns Kaiser Foundation Research … indications for colorectal cancer/polyposis (CRCP) genetic testing University of Washington, Seattle Gail Jarvik … University Wendy K. Chung Impact of return of incidental genetic test results to research participants in the genomic …
Research Funding
The Genotype-Tissue Expression (GTEx) Project will create a resource that researchers can use to study how inherited changes in genes lead to common diseases
… on behalf of GTEx. Until now, no project has analyzed genetic variation and expression in as many tissues in such a …
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.
… of Alabama at Birmingham Heersink School of Medicine  Our Genetic Testing Service is in the design phase, and we hope … UAB physician can use to ask for assistance in ordering genetic testing. The initial contact will be a Genetic Counseling Assistant (GCA). If the request is more …
Genomics and Medicine
The categories for the notable accomplishments of research are defined as research that uses genomics to generate or study.
… a disease or condition. Pharmacogenomics How a person’s genetic variation affects how they respond to medications. … vitro technologies or model organisms. Sequencing Use of genetic sequencing for patients’ medical care. Variant Classification How a genetic alteration influences an individual's susceptibility …
Event
On June 26, 2024, NHGRI hosted an application webinar for the ML/AI Tools to Advance Genomic Translational Research (MAGen) notice of funding opportunities (NOFOs) (to be published).
… precision of predicting how individuals with pathogenic genetic variants manifest disease. The objective is to … disease development in individuals carrying pathogenic genetic variants within a research consortium, ML/AI Tools to …