Have the minimum features implemented and reliable.

• Users should be able to point to their files and have the application render M/F/P & Alt Caller on Circos
• Users should also be able to inspect variants, their overlapped genes, and associations (phenotype/disease). They should also be able to inspect these associations with respect to the samples phenotypes.
• Users should be able to curate variants (delete them if they aren't interested in them)