Principles & Policies

Clinical & Phenotypic Data Capture (Clin/Pheno) Work Stream Cloud Work Stream Data Security Work Stream Data Use & Researcher Identity (DURI) Work Stream Discovery Work Stream Genomic Knowledge Standards (GKS) Work Stream Large-Scale Genomics (LSG) Work Stream Regulatory & Ethics Work Stream (REWS)

Authorisation and Authentication Infrastructure (AAI) Passports Beacon Browser Extensible Data (BED) Categorical Variation Representation Specification (Cat-VRS) Clinical Data Sharing and Consent 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 Pathogen Genomic Data Sharing: Bridging the Sovereignty and Access Divide Ethical Provenance Toolkit Ethics Review Recognition Policy Experiments Metadata Checklist (Expmeta) 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 Genetic Data Encryption (Crypt4GH) Genetic Discrimination Toolkit Genetic Variation Formats (VCF) htsget Machine Readable Consent Guidance (MRCG) Pedigree Phenopackets Policy on Clinically Actionable Genomic Research Results refget Sequences Responsible Data Sharing to Respond to the COVID-19 Pandemic: Ethical and Legal Considerations 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 Specification (VRS) Whole Genome Sequencing (WGS) Quality Control (QC) Standards Workflow Execution Service (WES) Your DNA, Your Say (Participant Values Survey)

Code of Ethics and Community Conduct (CECC)