Simplify your cancer risk assessment for breast and ovarian cancer, multiple genes, and non-cancer conditions to one click, launched within pedigrees.
Never enter the same information twice, compare GAIL, IBIS, PREMM5, and BOADICEA models with one click within pedigrees. Read about the specific cancers, mutations, and additional risk calculations available.
Save 45 minutes per patient—7.5 hours a week—in administrative paperwork. Harness that reclaimed time for patient care instead.
Seeing members of the same family together has never been easier. Manage a family’s genetic information all in one place.
Our Cancer Risk Assessment tool calculates risk probability for multiple genes, Breast and Ovarian cancer, as well as non-cancer conditions, while integrating seamlessly into your existing workflow, simplifying and unifying cancer genetics.
For breast cancer, GAIL, IBIS, and BOADICEA calculate lifetime risk, IBIS and BOADICEA calculate 10 year risk, and GAIL and BOADICEA calculate 5 year risk. For ovarian cancer, BOADICEA provides 5 year, 10 year, and lifetime risk calculations.
The PREMM5 model for Lynch Syndrome calculates the probability of mutation for MLH1, MSH2, MSH5, MSH6, PMS2, and EPCAM genes, while BOADICEA provides the probability of mutation for CHEK2, ATM, BRCA1, BRCA2, and PALB2 genes.
PhenoTips includes additional risk calculations such as an aortic root calculator for Marfan Syndrome, and will be updating the Cancer Risk Assessment tool to include risk calculations for Familial Hypercholesterolemia.
Eliminate all redundant data re-entry by integrating your complete solution for medical genetics with your EMR
Learn MoreWhen combined with Pre-Visit Patient Questionnaires, flag high-risk patients before their first appointment.
Save a timestamped PDF to your device complete with all calculations and model responses.
Discover your cancer genetics workflow, simplified to one click within pedigrees.
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