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.
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.
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Read news, stories, and insights from the forefront of genomic and clinical data use.
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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.
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View the latest GA4GH updates, Genomics and Health News, Implementation Notes, GDPR Briefs, and more.
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24 Jan 2019
A new transcontinental project will pilot nearly all of GA4GH’s genomic data standards to enable a virtual cohort of more than 1.4 million individuals from Europe, Canada, and Africa.
A new transcontinental project led by EMBL’s European Bioinformatics Institute (EMBL-EBI) will pilot nearly all of GA4GH’s genomic data standards to enable a virtual cohort of more than 1.4 million individuals from Europe, Canada, and Africa.
In particular, the Common Infrastructure for National Cohorts in Europe, Canada and Africa (CINECA) project will utilise GA4GH Data Use and Researcher Identity standards to allow registered researchers to analyse population-scale genomic and biomolecular data through a federated cloud-based network in a way that meets all ethical and security requirements for the international sharing of health data.
“The goal of this implementation is to accelerate the process of accessing datasets in a safe and secure way,” said Thomas Keane, team lead of the European Genome-Phenome Archive (EGA) at EMBL-EBI and co-lead of the GA4GH Large Scale Genomics Work Stream. “All the control of the datasets remains with the local cohorts, as we’re not trying to create a centralised resource, but a federated one.”
Rapid access to clinical research data allows scientists to share their findings and reduce the need to duplicate costly studies. This accelerates research and helps advance benefits to patients through the responsible sharing of genetic, phenotypic, and life-style data on an unprecedented scale.
“By enabling access to genetic data from diverse human populations, CINECA will support the development of treatments tailored to each individual patient’s genetic profile, the ultimate goal of personalised medicine,” Keane said. “Clinicians need to be able to compare a patient’s genome to a large set of healthy people and sick people, in order to understand the underlying genetics of the patient. And by ‘large,’ we mean hundreds of thousands or even millions of other people,” Keane said.
Several of the 18 CINECA partner organisations are active GA4GH contributors, including long-time GA4GH collaborators ELIXIR and H3Africa and GA4GH Driver Projects CanDIG and ENA/EVA/EGA. Spanning three continents, CINECA will use GA4GH standards to bring together data from 11 diverse cohorts in rare disease, common disease, and population health studies.
“The technical goals we have set for ourselves are ambitious,” said Mike Brudno, PI of the CanDIG project, Senior Scientist at The Hospital for Sick Children (SickKids) in Toronto, and a GA4GH Steering Committee member. “But CanDIG has extensive experience working with CINECA partner projects EGA and ELIXIR through their participation as peer Driver Projects within GA4GH. Building on what our projects have already done alone and together, we’re confident that we can not only meet those goals, but build open-source standards-based solutions for the entire community.”
Nicola Mulder, Head of Computational Biology at University of Cape Town and Principle Investigator of H3ABioNet, a Pan-African bioinformatics network for H3Africa, said the project “provides an avenue for us to align with international best practices, and contribute to these from an African and resource-limited perspective. At the same time as contributing our own expertise in working with diverse African genetic data, we hope to gain experience in new technologies for data sharing and clinical implementations.”
The CINECA project is funded by the EU through the Horizon 2020 Research and Innovation Programme and the Canadian Government through the Canadian Institutes for Health Research.