Search Results
Facet (Page)
Refine Your Search
Audiences
Content Formats
Events
Sections
Divisions
Programs
- Developmental Genotype-Tissue Expression (dGTEx)1
- Multi-Omics for Health and Disease (Multi-Omics)1
- Genomics-Enabled Learning Health Systems (gLHS)2
- Genome Technology Program2
- Enhancing Opportunities in Computational Genomics and Data Science1
- Impact of Genomic Variation on Function (IGVF) Consortium1
- Clinical Genome (ClinGen) Resource1
- Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium1
- NHGRI Genomic Data Science Analysis, Visualization and Informatics Lab-space (AnVIL)1
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium1
News Release
Genomic variants that increase risk of kidney disease are found in nearly one-third of West Africans
A study from researchers at National Institutes of Health (NIH) and their collaborators revealed a significant genetic risk factor for kidney disease in people of West African ancestry.
… on Genomics and Global Health at NIH’s National Human Genome Research Institute (NHGRI). “By comparing this study to previous studies involving the African American population, we can … seen most often in people of West African ancestry, other studies have found these variants in people from Europe, …
The Genomics Landscape
In the October 2024 issue of The Genomics Landscape, NHGRI Director Eric Green welcomes James Thomas as the new director for NIH Intramural Sequencing Center (NISC).
… website . Applications close in January.  All the best, … Genome-wide detection of somatic mosaicism at short tandem repeats … intramural research community, enabling powerful genomics studies across institutes and centers.  “For more than 25 …
Event
On November 5-9, 2024, the National Human Genome Research Institute (NHGRI) will participate in the ASHG Annual Meeting - the world's largest human genetics and genomics meeting and exposition.  The annual meeting provides a forum for the presentation and discussion of cutting-edge science in all areas of human genetics.Â
… Wednesday, November 6, 2:30 – 4:30 p.m. Anas Awan Phenome-wide association study of MTHFR variant in UK Biobank and All of … Methylation and Transcriptomic Analyses with Whole Genome Sequencing YieldsNovel Insights into SARS-CoV-2 in …
File
… improve genomic discovery and clinical implementations? • Genome -wide genotyping • GWAS • Clinical implementation Pilots • … across an entire collaborative Network • Phenome -wide association studies ( PheWAS) • 3144 SNPS present in NHGRI …
File
… Report'From'A'Planning'Workshop' ' for'the'National'Human'Genome'Research'Institute ' “ … :# ¥ Using#genomics#assays#for#genome+wide#identification#of#functional#elements# ¥ … genome annotation for Eric Boerwinkle genotype-phenotype association studies 16 8:25 a.m. – 8:50 a.m. Hirschsprung …
File
… National Advisory Council for Human Genome Research May 19, 2014 Concept Clearance for RFA s … demonstrated the robustness of EMR phenotyping for genome -wide studies , defined approaches for enhancing privacy of … phenotypes and has continued GWAS and phenome -wide association studies ( PheWAS, which it helped to originate ) …
File
… NHGRI Planning Workshop Recap- From Genome Function To Biomedical Insight: ENCODE And Beyond … • Make resource freely available to community for use in studies of: – genetic basis of disease – gene regulation 4 … a few weeks 13 Workshop Recommendations • Continue genome-wide identification of functional elements • Add functional …
File
… Concept Clearance National Advisory Council for Human Genome Research September 8, 2014 1) Should NIH fund a … Inherited Disease Research • SNP Genotyping - Human Genome Wide Association Studies - Custom Genotyping - Focused Content …
File
… Di Francesco, Ajay Pillai, Adam Felsenfeld Division of Genome Sciences, NHGRI, NIH May 18, 2020 NACHGR Council … tech advances to the level where SMPS can be used for genome-wide surveys; • Improve speed, sensitivity, quantitation and …
File
… Mendelian diseases in two main ways. The first is to use genome-wide sequencing (mostly whole exome sequencing) to discover … These variants are displayed in custom tracks on UCSC Genome Browser. x All CMGs deposit to dbGaP the data …