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
Driver Projects
- All of Us Research Program
- Australian Genomics
- Autism Sharing Initiative
- Biomedical Research Hub (BRH)
- BRCA Challenge
- Canadian Distributed Infrastructure for Genomics (CanDIG)
- Clinical Genome Resource (ClinGen)
- ELIXIR Beacon
- ELIXIR Cloud and AAI
- ENA / EVA / EGA
- EpiShare
- EUCANCan
- European Joint Programme on Rare Disease (EJP RD)
- GEnome Medical alliance Japan (GEM Japan)
- Genomics England
- Human Cell Atlas
- Human Heredity and Health in Africa (H3Africa)
- Human Pangenome Project (HPP)
- ICGC ARGO
- Immunotherapy Centers of Research Excellence (imCORE®)
- International Precision Child Health Partnership (IPCHiP)
- Matchmaker Exchange
- Monarch Initiative
- National Cancer Institute Cancer Research Data Commons (NCI CRDC)
- National Cancer Institute Genomic Data Commons (NCI GDC)
- NHLBI BioData Catalyst® (BDC)
- NIH Cloud Platform Interoperability (NCPI) effort
- Repository of the International Fetal Genomics Consortium (RIFGC)
- Swiss Personalized Health Network (SPHN)
- Trans-Omics for Precision Medicine (TOPMed)
- Variant Interpretation for Cancer Consortium (VICC)
Implementations
- All of Us Researcher Workbench
- ARGO Data Platform
- Australian Genomics Data Management Systems
- BioBank Japan (BBJ)
- Biomedical Research Hub (BRH)
- BRCA Exchange
- CanDIG V2
- ClinGen Knowledge-base
- cwl-WES
- EJP-RD Beacon-in-a-Box
- EJP-RD Virtual Platform
- ELIXIR BioContainers
- ELIXIR Cloud & AAI
- ELIXIR European Genome-phenome Archive (EGA)
- ELIXIR-Beacon
- ENCODE RNAExpression report
- EpiShare Platform
- Federated EGA
- Funnel
- GA4GH TES on Azure
- Genomics England Research Environment
- GTEx RNAget
- H3ABionet
- Human Cell Atlas (HCA) Data Portal
- Life Science AAI
- Medical Genomics Japan Variant Database (MGeND)
- MSSNG Genetics Application System
- National Genomic Information System (NGIS)
- NCI Data Commons Framework
- NCPI Interoperability Projects and partners
- NHLBI BioData Catalyst® (BDC)
- NHLBI TOPMed BioData Catalyst
- Omics AI
- TESK
- The Exomiser
- TogoVar
- Tohoku Medical Megabank Project (ToMMo)
- Variant Interpretation for Cancer Consortium (VICC) Meta-Knowledgebase (v1)
Products
- Authorisation and Authentication Infrastructure (AAI)
- Bad Actors in Research Environments (BARE)
- Beacon
- Browser Extensible Data (BED)
- Categorical Variation (CatVar)
- Clinical Data Sharing and Consent
- Cloud Security and Privacy
- Cohort Representation
- Consent Policy
- Consent Toolkit
- CRAM
- Data Access Committee Review Standards (DACReS) Toolkit
- Data Connect
- Data Model and Schema Consensus (DaMaSC)
- Data Privacy and Security Policy
- Data Repository Service (DRS)
- Data Security Infrastructure Policy (DSIP)
- Data Use Ontology (DUO)
- Diversity in Datasets
- Ethical Preparedness for Pandemics and Epidemics (EPPE) Framework
- Ethical Provenance Toolkit
- Ethics Review Recognition Policy
- Experiments Metadata Standard
- Family History Toolkit
- Framework for Involving and Engaging Participants, Patients, and Publics in Genomics Research and Health Implementation
- Framework for responsible sharing of genomic and health-related data
- GDPR & International Health Data Sharing Forum
- Genetic Data Encryption (Crypt4GH)
- Genetic Discrimination Toolkit
- Genetic Variation Formats (VCF)
- htsget
- Machine Readable Consent Guidance (MRCG)
- Passports
- Pedigree
- Pharmacogenomics Data Standardisation
- Phenopackets
- Policy on Clinically Actionable Genomic Research Results
- Public Attitudes for Genomic Policy — Blog Posts
- refget
- Responsible Data Sharing to Respond to the COVID-19 Pandemic: Ethical and Legal Considerations
- Risk Assessment Methodology for Software Stacks
- RNAget
- SAM/BAM
- Sequence Annotation (SA)
- Service Info
- Service Registry
- Task Execution Service (TES)
- Tool Registry Service (TRS)
- Variant Annotation (VA)
- Variant Benchmarking Tools
- Variation Representation (VRS)
- WGS Quality Control Standards
- Workflow Execution Service (WES)
- Your DNA, Your Say (Participant Values Survey)