Our customizable knowledgebases act as a collection of annotated associations between genomic aberrations and related phenotypes. Our machine learning leverages growing data.
Each entry in the knowledgebase is a documented genomic aberration association, which is relevant to understanding genomic drivers of disease and treatment response.
Doctors and qualified personnel are allowed to curate this knowledgebase and to continue to enter observations.
The goal is to provide consistent and transparent clinical interpretation of patient genomic data for:
1. Improved diagnosis and treatment options
2. Targeted therapy development: research and discovery of variant associations for new therapeutic innovations