Study content IS available for download

A list of studies in HGVbaseG2P is now available for download. The data available includes non-sensitive data such as PubMed identifier, DOI, links to the study in HGVbaseG2P, phenotypes, the number of markers imported and links to the original resources where the association data was downloaded.

To view the Study list please click here.

Association content is NOT available for download at the present time

The current problem is the field's uncertainty as to when, where and how one can infer the presence of a research subject in summary level association data. This follows a paper on this subject Homer et al., PLoS Genet. 4, e1000167 (2008) which led to the shutting down of all data sharing.

We are now working on many levels to define the real 'risks' and convince the field leaders to permit more open data sharing again (of summary level statistics). Until some real progress is made on those fronts then we feel unable to draw any arbitrary line in allowing some bulk downloads and not others.

We also include links to all the sources from which we have gathered the data in our system, so that others can obtain the content from its origin as well.

Marker content is NOT available for download at the present time

We hope to make our marker content (dbSNP) available for bulk download and via our BioMart soon.

Other Information

In the future we do hope to make all the content freely downloadable again.

If you have any questions please contact us at help@hgvbaseg2p.org

The HGVbaseG2P Team