Login to HeartsMart to use the interactive query builder to:
- Identify cohorts of subjects.
- Locate raw and analyzed molecular data sets.
- Export phenotype data for further investigation.
- Download data files matching your criteria.
Don't have access? Click here to request access
June 13, 2022
Clinical Data Refresh (Updated as of May 31, 2022):
April 21, 2022
Clinical Data Refresh (Updated as of March 31, 2022):
March 11, 2022
Clinical Data Refresh (Updated as of February 28, 2022):
Last data update
Genotyping, Candidate Gene Evaluation, and Whole Exome cores can submit data by following these procedures.
Clinical Phenotypes for existing samples can be provided to the core by using our REDCap database.
Confirmation Core CNV and variant call confirmations can also be provided to the core by using our REDCap database.
Molecular data including whole whole exome, target sequencing, and SNP genotyping results are available via our secure, high-speed Aspera server.
Check out our Aspera getting started guide.
Have a question or need some help? Leave the PCGC Support Team a message using our support form.