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.
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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.
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This subset of Organisational Members whose networks or infrastructure align with GA4GH priorities has made a long-term commitment to engaging with our community.
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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.
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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.
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8 Jun 2018
The new Framework developed by GA4GH Member organization H3Africa aims to guide ethically responsible biomedical research in Africa and builds on the work of the GA4GH Regulatory and Ethics Work Stream.
In its first five years, the Human Heredity and Health in Africa (H3Africa) Initiative involved 75,000 participants across the African continent in a variety of genomics-based research projects. Its research network spanned more than 500 investigators in 27 countries and its members began to share data through the H3ABioNet — a federated bioinformatics network chaired by Nicola Mulder, a long time leader in the Global Alliance for Genomics and Health and Professor of Computational Biology Group at the University of Cape Town.
This approach brought with it the introduction of open sharing policies and the need for informed consent — entirely new challenges for many of the African investigators and institutions.
“About two years into H3Africa, we realized this really was about a sea change in how people perceive research and ethics and there was a lot of apprehension about this idea of sharing on the continent,” says Jantina de Vries, Associate Professor Bioethics at the University of Cape Town.
That realization led de Vries and her colleagues of the H3Africa Working Group on Ethics, which she chaired at the time, to meet with members of the ethics committees around Africa who were reviewing H3Africa research studies and start to understand their concerns and come up with a path forward. The result of these efforts — three years in the making — is the Ethics and Governance Framework for Best Practice in Genomic Research and Biobanking in Africa. The framework was recently discussed in an open letter to AAS Open Research, as well as a news article and an editorial piece in the journal Nature. The H3Africa Framework builds on the format used by the Framework for Responsible Sharing of Genomic and Health-related Data, developed by the GA4GH Regulatory and Ethics Work Stream, of which de Vries is a founding member.
“Over the course of those three years of engagement with ethics committees, we heard this repeated call for high level guidance to address some of those issues — the concept of data sharing, sample sharing, future use, broad consent, and the like,” says de Vries. “The framework example from the GA4GH led me to think of that as a good format for offering that high level guidance.”
Like the GA4GH Framework, the new document puts forth a series of core principles and elements to guide research and the sharing of samples and data. But these are specifically tailored for the African research context. The core principles state that research making use of African data should (i) be sensitive to and respectful of African values and culture, (ii) benefit African people, (iii) include genuine and active intellectual participation of African investigators, and (iv) promote respect, fairness, equity, and reciprocity.
“We tried to pick out what we think are the predominant ethical concerns in open science in the African research context,” says de Vries. “Where capacity, exploitation and unfairness in collaboration remain real problems, emphasis on something like intellectual African leadership is really important.”
“These countries have been exploited for so long in terms of sample collection, some are suspicious of international collaborations, and they’re less open to sharing and open science,” said Mulder, who is helping spearhead the next phase of the consortium. “So having this new resource will be invaluable in engaging ethics committees going forward.”
In its next phase, H3Africa aims to collect genomic data on 100,000 participants — including whole exome, whole genome, and genotype data. The consortium has grown to include 48 research projects across 34 African countries and is well on its way to fulfilling this goal. In particular, future research will make use of the H3Africa chip which has been customized for African populations, Mulder says. The data analysis work will be supported by H3ABioNet using a variety of standards developed by GA4GH.