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- Developmental Genotype-Tissue Expression (dGTEx)1
- Multi-Omics for Health and Disease (Multi-Omics)1
- Ethical, Legal and Social Implications (ELSI) Research Program6
- Genomics-Enabled Learning Health Systems (gLHS)2
- Genetic Architecture of Complex Traits1
- Genome Technology Program5
- Enhancing Opportunities in Computational Genomics and Data Science1
- Human Genome Reference Program (HGRP)2
- Impact of Genomic Variation on Function (IGVF) Consortium3
- Advancing Genomic Medicine Research (AGMR)1
- Encyclopedia of DNA Elements (ENCODE) Project1
- Molecular Phenotypes of Null Alleles in Cells (MorPhiC)1
- Clinical Genome (ClinGen) Resource1
- Genomic Innovator Awards2
- Polygenic RIsk MEthods in Diverse populations (PRIMED) Consortium1
- NHGRI Genomic Data Science Analysis, Visualization and Informatics Lab-space (AnVIL)2
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium2
Healthcare Provider Education Resources
An online repository of peer-reviewed collections of genomics educational materials for genetic counselors, nurses, pharmacists, physician assistants, and physicians.
AnVIL
The Data Use Oversight System (DUOS) is a semi-automated study registration and DAR management service informed by the GA4GH DUO standard, which enables the secondary use of human genomics and other controlled-access data in compliance with the informed consent of a study’s participants.
… Algorithms to Improve Decision-Making Workflows for Genomic Data Access and Management .” Biopreservation and … et al. “ Achieving Procedural Parity in Managing Access to Genomic and Related Health Data: A Global Survey of Data … Health Science Policy Analyst, NHGRI NHGRI Policy Panel: Genomic Data Sharing Policies: Challenges and Innovative …
Research Funding
The GREGoR (formerly the Mendelian Genomics Research Consortium) is aimed at significantly increasing the proportion of Mendelian disorders with an identified genetic cause through enhanced data sharing, collaboration and an increased focus on the application of new technologies, sequencing strategies and analytical approaches.
… Luria-O’Donnell Broad Institute Broad Institute Mendelian Genomic Research Center U01HG011755 Jennifer Posey Baylor …
Research Funding
Building upon a foundation of quantitative genetics laid over a century ago, applying modern genomic approaches to resolve how genetic and non-genetic factors shape variation in human diseases and traits.
… the growing availability of large-scale human genetic, genomic, and phenotypic data affords opportunities to revisit … genetics laid over a century ago, applying modern genomic approaches to resolve how genetic and non-genetic … genetics laid over a century ago, applying modern genomic approaches to resolve how genetic and non-genetic …
Research Funding
The developmental Genotype-Tissue Expression initiative's goal is to catalog and analyze transcriptional profiles from a wide variety of tissues from the pediatric period, including neonates through adolescents, in a post-mortem setting.
… of human tissues throughout development, filling a gap in genomic databases across developmental stages. The Non-Human …
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
Research Funding
The Multi-Omics for Health and Disease Consortium aims to advance the application of multi-omic technologies to study health and disease in ancestrally diverse populations.
… will utilize high-throughput molecular assays to produce: genomic, epigenomic, transcriptomic, proteomic, and … Advisory Council Meeting : Concept Document Slides … NIH awards $50.3 million for “multi-omics” research on human …
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.
… Optimize the integration of large-scale, harmonized genomic and phenotype data. Starting June 2021, the seven … integration and analysis will occur largely on NHGRI's Genomic Data Science Analysis, Visualization, and Informatics … (U01 Clinical Trial Not Allowed) … Press Release: NIH awards $38 million to improve utility of polygenic risk …
Research Funding
The Non-Coding Variants Program explores which variants in a region associated with a disease or trait cause the higher risk for the disease or trait
… make predictions about a person's risk of disease. The six awards funded in the first round of this RFA use a range of …
Research Funding
MorPhiC aims to develop a consistent catalog of molecular and cellular phenotypes for null alleles for every human gene by using in-vitro multicellular systems.
… in pathways and networks, which is one of the compelling genomic research projects outlined in the NHGRI Strategic …