About us
Learn how GA4GH helps expand responsible genomic data use to benefit human health.
Learn how GA4GH helps expand responsible genomic data use to benefit human health.
Our Strategic Road Map defines strategies, standards, and policy frameworks to support responsible global use of genomic and related health data.
Discover how a meeting of 50 leaders in genomics and medicine led to an alliance uniting more than 5,000 individuals and organisations to benefit human health.
GA4GH Inc. is a not-for-profit organisation that supports the global GA4GH community.
The GA4GH Council, consisting of the Executive Committee, Strategic Leadership Committee, and Product Steering Committee, guides our collaborative, globe-spanning alliance.
The Funders Forum brings together organisations that offer both financial support and strategic guidance.
The EDI Advisory Group responds to issues raised in the GA4GH community, finding equitable, inclusive ways to build products that benefit diverse groups.
Distributed across a number of Host Institutions, our staff team supports the mission and operations of GA4GH.
Curious who we are? Meet the people and organisations across six continents who make up GA4GH.
More than 500 organisations connected to genomics — in healthcare, research, patient advocacy, industry, and beyond — have signed onto the mission and vision of GA4GH as Organisational Members.
These core Organisational Members are genomic data initiatives that have committed resources to guide GA4GH work and pilot our products.
This subset of Organisational Members whose networks or infrastructure align with GA4GH priorities has made a long-term commitment to engaging with our community.
Local and national organisations assign experts to spend at least 30% of their time building GA4GH products.
Anyone working in genomics and related fields is invited to participate in our inclusive community by creating and using new products.
Wondering what GA4GH does? Learn how we find and overcome challenges to expanding responsible genomic data use for the benefit of human health.
Study Groups define needs. Participants survey the landscape of the genomics and health community and determine whether GA4GH can help.
Work Streams create products. Community members join together to develop technical standards, policy frameworks, and policy tools that overcome hurdles to international genomic data use.
GIF solves problems. Organisations in the forum pilot GA4GH products in real-world situations. Along the way, they troubleshoot products, suggest updates, and flag additional needs.
NIF finds challenges and opportunities in genomics at a global scale. National programmes meet to share best practices, avoid incompatabilities, and help translate genomics into benefits for human health.
Communities of Interest find challenges and opportunities in areas such as rare disease, cancer, and infectious disease. Participants pinpoint real-world problems that would benefit from broad data use.
The Technical Alignment Subcommittee (TASC) supports harmonisation, interoperability, and technical alignment across GA4GH products.
Find out what’s happening with up to the minute meeting schedules for the GA4GH community.
See all our products — always free and open-source. Do you work on cloud genomics, data discovery, user access, data security or regulatory policy and ethics? Need to represent genomic, phenotypic, or clinical data? We’ve got a solution for you.
All GA4GH standards, frameworks, and tools follow the Product Development and Approval Process before being officially adopted.
Learn how other organisations have implemented GA4GH products to solve real-world problems.
Help us transform the future of genomic data use! See how GA4GH can benefit you — whether you’re using our products, writing our standards, subscribing to a newsletter, or more.
Help create new global standards and frameworks for responsible genomic data use.
Align your organisation with the GA4GH mission and vision.
Want to advance both your career and responsible genomic data sharing at the same time? See our open leadership opportunities.
Join our international team and help us advance genomic data use for the benefit of human health.
Share your thoughts on all GA4GH products currently open for public comment.
Solve real problems by aligning your organisation with the world’s genomics standards. We offer software dvelopers both customisable and out-of-the-box solutions to help you get started.
Learn more about upcoming GA4GH events. See reports and recordings from our past events.
Speak directly to the global genomics and health community while supporting GA4GH strategy.
Be the first to hear about the latest GA4GH products, upcoming meetings, new initiatives, and more.
Questions? We would love to hear from you.
Read news, stories, and insights from the forefront of genomic and clinical data use.
Attend an upcoming GA4GH event, or view meeting reports from past events.
See new projects, updates, and calls for support from the Work Streams.
Read academic papers coauthored by GA4GH contributors.
Listen to our podcast OmicsXchange, featuring discussions from leaders in the world of genomics, health, and data sharing.
Check out our videos, then subscribe to our YouTube channel for more content.
View the latest GA4GH updates, Genomics and Health News, Implementation Notes, GDPR Briefs, and more.
Discover all things GA4GH: explore our news, events, videos, podcasts, announcements, publications, and newsletters.
Genomic data initiatives around the world develop and pilot GA4GH products.
A Driver Project is an initiative that shapes GA4GH products and applies them to real genomic data. Driver Projects range from national health services to rare disease networks to cancer data centres. All are committed Organisational Members that give voice to the broader genomics community and ensure GA4GH products serve real needs. Driver Projects implement and promote GA4GH products in their local networks. All proposed products must secure interest from two Driver Projects before development starts.
Leads historic effort to gather data from one million or more people in the U.S.
See moreLinks organisations to integrate genomic medicine into Australian healthcare
See moreBuilds the first federated, global network for sharing autism data
See moreMakes international patient data available for research via federation
See moreBuilds central resources defining the clinical relevance of genes and variants
See moreDevelops a GA4GH-compliant federated cloud computing network in Europe
See moreSets the foundations for making cancer research data usable across Europe
See moreProvides a secure service for storing and sharing human genetic, phenotypic, clinical, and other “omics” data for research projects
See moreFederating genomic and health data access across Europe
See moreLinks rare disease care, research, and medical innovation in 35 countries
See moreProvides data access and tools to help everyone benefit from genomic healthcare
See moreCreates comprehensive maps of all human cells for researchers around the globe
See moreBuilds a pan-continental network to study environmental and genetic health factors
See moreGives access to genomes that represent the diversity of the human population
See moreShares knowledge from cancer patient genomes and health-related data on a cloud-based system
See moreImproves impact of cancer immunotherapies via a collaborative research network
See moreImproves child health and rare disease outcomes through collaborative genomics
See moreMatches individuals with rare disease by candidate gene and phenotypes to find gene-disease relationships
See moreProvides a platform for connecting phenotypes to genotypes across species
See moreProvides cloud infrastructure to share, analyse, and visualise cancer data
See moreOffers data, tools, apps, and workflows to share, store, and compute on datasets
See moreEnables interoperability and end-user analyses of NIH cloud controlled access datasets
See moreUnlocking the potential of genomic data for Canada’s future
See moreUnites pregnancy sequencing projects focused on maternal-foetal and neonatal health
See moreStandardises cancer variant knowledge to enable precision oncology
See more