About us
Learn how GA4GH helps expand responsible genomic data use to benefit human health.
Sitemap
Explore the sitemap of all pages below, including information about Work Streams, products, implementations, and Driver Projects.
Pages
- Home
- About us
- Our community
- What we do
- Our products
- Get involved
- All news and events
- Code of Conduct
- Constitution
- Copyright Policy
- Framework for responsible sharing of genomic and health-related data
- Privacy Policy
- Resource library
- Search
- Sitemap
- Terms and conditions of use of site
- Join a Work Stream
- Join as an Organisational Member
- Join our leadership
- Join our staff
Driver Projects
- ELIXIR
- ELIXIR Cloud and AAI
- Swiss Personalized Health Network (SPHN)
- EpiShare
- Human Heredity and Health in Africa (H3Africa)
- Autism Sharing Initiative
- European Joint Programme on Rare Disease (EJP RD)
- GEnome Medical alliance Japan (GEM Japan)
- EUCANCan
- Variant Interpretation for Cancer Consortium (VICC)
- Trans-Omics for Precision Medicine (TOPMed)
- National Cancer Institute Cancer Research Data Commons (NCI CRDC)
- National Cancer Institute Genomic Data Commons (NCI GDC)
- Monarch Initiative
- Matchmaker Exchange
- ICGC ARGO
- Human Cell Atlas
- Genomics England
- ENA / EVA / EGA
- ELIXIR Beacon
- Clinical Genome Resource (ClinGen)
- Canadian Distributed Infrastructure for Genomics (CanDIG)
- BRCA Challenge
- Australian Genomics
- All of Us Research Program
Products
- Variant Benchmarking Tools
- Family History Toolkit
- Pharmacogenomics Data Standardisation
- WGS Quality Control Standards
- Bad Actors in Research Environments (BARE)
- Consent Toolkit
- SAM/BAM
- Genetic Discrimination Toolkit
- Cohort Representation
- Your DNA, Your Say (Participant Values Survey)
- Workflow Execution Service (WES)
- Variation Representation (VRS)
- Variant Annotation (VA)
- Tool Registry Service (TRS)
- Task Execution Service (TES)
- Service Registry
- Service Info
- Sequence Annotation (SA)
- RNAget
- Risk Assessment Methodology for Software Stacks
- Responsible Data Sharing to Respond to the COVID-19 Pandemic: Ethical and Legal Considerations
- refget
- Public Attitudes for Genomic Policy — Blog Posts
- Policy on Clinically Actionable Genomic Research Results
- Phenopackets
- Pedigree
- Machine Readable Consent Guidance (MRCG)
- htsget
- Genetic Variation Formats (VCF)
- Genetic Data Encryption (Crypt4GH)
- GDPR & International Health Data Sharing Forum
- Passports
- Framework for responsible sharing of genomic and health-related data
- Framework for Involving and Engaging Participants, Patients, and Publics in Genomics Research and Health Implementation
- Ethics Review Recognition Policy
- Ethical Provenance Toolkit
- Diversity in Datasets
- Data Use Ontology (DUO)
- Data Security Infrastructure Policy (DSIP)
- Data Repository Service (DRS)
- Data Privacy and Security Policy
- Data Connect
- Data Access Committee Review Standards (DACReS) Toolkit
- Consent Policy
- CRAM
- Cloud Security and Privacy
- Clinical Data Sharing and Consent
- Browser Extensible Data (BED)
- Beacon
- Authorisation and Authentication Infrastructure (AAI)