Table 1 Features of three web-based personal genomic data sharing projects
Name of the project | Type of data they collect | Goals |
|---|---|---|
Consent to research (Portable Legal Consent) | exome, whole-genome sequence, electronic health records or family history | To create large datasets of user-contributed health and genomic data that are easier to re-use, to promote collaborations and innovation around health and genomic research |
Free the data | Mutation reports for BRCA1/2, a variety of health information | To invite clinicians and individuals to donate their mutations and associated clinical data in order to be deposited in ClinVar and other open-access databases |
Genomes unzipped (GNZ) | Genotypes obtained from various genetic test providers, release of more data up to and including whole-genome sequencing is envisioned | To use the data provided by participants and other GNZ community members both to perform scientific analyses and as a basis for communicating about genetics to a broader audience |