Added
- Profiling feature added. Each sample gets a profile based on the genotypes for
a set of high maf variants.
- High maf variants used in profiling is loaded into DB via CLI
- Reject loading a case if a similar profile already exists for any of the samples
- Statistics of the profiles in DB can be generated through CLI
- use bulk operations when deleting variants
- Compatible with GRCh38
- Option to include case count when querying for a variant
Fixed
- Use correct fields in index