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.
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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.
17 Mar 2022
Please join us in welcoming our four new work streams and FASP co-leads to the GA4GH community!
The Global Alliance for Genomics and Health (GA4GH) welcomes four new members to its Steering Committee.
Dr Ian Fore of the NIH National Cancer Institute will be joining the Federated Analysis Systems Project (FASP) with current co-leads Max Barkley and Dr Brian O’Connor. Dr Dianne Nicol of the University of Tasmania will be joining the Regulatory & Ethics Work Stream (REWS) with co-lead Dr Yann Joly. Dr Mélanie Courtot of the Ontario Institute of Cancer Research (OICR) will be joining the Clinical & Phenotypic Data Capture (Clin/Pheno) with co-lead Dr David Hansen. Dr Lucila Ohno-Machado of the University of California San Diego will be joining the Data Security Work Stream (DSWS) with co-lead David Bernick.
Dr Fore is a senior biomedical informatics program manager at the NIH National Cancer Institute Center for Biomedical Informatics & Information Technology (CBIIT), specialising in integrating data from both basic and clinical science. His current contributions focus on the core components of the Cancer Research Data Commons (CRDC), which enable data integration, topics such as subject and specimen data, identifiers and data aggregation. Beyond the technology, interoperability is also about how humans work together, and Dr Fore leads CBIIT’s One Team One Mission program to enhance collaboration within and between projects. Dr Fore previously led CBIIT’s programs in biorepository and pathology informatics. He contributed to the NIH Big Data to Knowledge initiative and the NIH Data Commons Pilot Phase Consortium.
Dr Nicol stood down from her roles as Distinguished Professor of Law and Director of the Centre for Law and Genetics at the University of Tasmania at the end of 2021 but continues as Adjunct Professor. Dr Nicol is also the chair of the Australian National Health and Medical Research Council Embryo Research Licensing Committee. She was admitted as a barrister and solicitor to the Supreme Court of Tasmania and the High Court of Australia in 1998 and spent some time in legal practice. Her research background includes law and science, as she holds a PhD in cell and developmental biology. Dr Nicol’s teaching and research interests focus primarily on the interface between technology and the law, particularly the regulatory and ethical issues associated with genomics, stem cell and related health technologies and intellectual property law.
Dr Courtot is the director of Genome Informatics and incoming Principal Investigator at the Ontario Institute for Cancer Research (OICR). Her team develops new software, databases and other necessary components to store, organise and compute over the large and complex datasets being generated by OICR’s cancer research programs. Previously, she was the metadata standards coordinator for the archival and infrastructure team at the European Bioinformatics Institute (EMBL-EBI). Her background is in structural biochemistry, computer science and bioinformatics, with a focus on knowledge representation and semantic engineering. At EMBL-EBI, she designed tools to streamline multi-omics submissions and developed integrated metadata strategies across the institute’s archival resources and other projects such as FAIRPlus, focusing on data quality, semantic enrichment and standardisation for pharmaceutical and cohort data respectively. Dr Courtot is passionate about translational informatics — building intelligent systems to gain new insights and impact human health. She co-leads the Data Use and Cohort Representation subgroups for GA4GH, as well as cohort harmonisation efforts for Common Infrastructure for National Cohorts in Europe, Canada, and Africa (CINECA), the International HundredK+ Cohorts Consortium (IHCC) and the Davos Alzheimer’s Collaborative.
Dr Ohno-Machado received her medical degree from the University of São Paulo and her doctoral degree in medical information sciences and computer science from Stanford University. She is associate dean for informatics and technology, and the founding chair of the University of California San Diego (UCSD) Health Department of Biomedical Informatics, where she leads a group of faculty with diverse backgrounds in medicine, nursing, informatics and computer science. Before her current position, she was on faculty at Brigham and Women’s Hospital, Harvard Medical School and at the Harvard-MIT Division of Health Sciences and Technology. Dr Ohno-Machado is an elected fellow of the American College of Medical Informatics, the American Institute for Medical and Biological Engineering and the American Society for Clinical Investigation. She served as editor-in-chief for the Journal of the American Medical Informatics Association from 2011 to 2018. She directed the patient-centered Scalable National Network for Effectiveness Research, a clinical data research network with over 24 million patients and 14 health systems, as well as the NIH/BD2K-funded Data Discovery Index Consortium. She was one of the founders of UC-Research eXchange, a clinical data research network that connected the data warehouses of the five University of California medical centres. She now leads the California Precision Medicine Consortium for the All of Us Research Program, the RADx-rad Data Coordinating Center and research projects in the areas of privacy technology and data sharing.
Please join us in welcoming Drs Fore, Nicol, Courtot, and Ohno-Machado! The GA4GH Secretariat wishes all Work Streams and cross-Work-Stream projects successful endeavours for the rest of the year.
We would also like to take the time to thank our co-leads who are stepping down. Melissa Haendel, Jean-Pierre Hubaux, Ted Dove and Craig Voisin, thank you for the time and effort you have given to our community.