Entering edit mode
10.7 years ago
Devonj
▴
90
We are currently using 1000 genomes phase 1 and NHLBI Exome Sequencing Project data ( http://evs.gs.washington.edu/EVS/ ) data to determine variant allele frequency. Both of these are getting relatively old (in genomics terms)
I'm wondering if there are any larger datasets out there yet?
Thanks for the links but these are relatively unsatisfying. Was hoping for NGS based exome or whole genome data - perhaps I should have specified.
Then you can easily compute such values directly from currently available NGS data, e.g. COSMIC, TCGA, etc.