New in MutationForecaster®: Improved, more comprehensive Workflows!
MutationForecaster now generates comprehensive genome interpretation on-the-fly. The results from all of our gene variant interpretation modules (Shannon Splicing Mutation Pipeline, ASSEDA, VEP, and Veridical) can now be automatically processed by CytoVA to find mutated genes in the genome related to a particular phenotypes based on published literature. Results are also be immediately processed to find dysfunctional biochemical pathways common to multiple mutated genes. All of the results are directly imported to your own CUVD repository, where all the results for each variant are grouped together.
The process is completely unattended. Start the Workflow for an variant set from an exome or genome sequence; several hours later all of the analyses are finished for you to review in your own CUVD database.
