Our platforms assist in analyzing clinical genomics data, enhancing the early detection, diagnosis, and prognosis for patient care, with a specific emphasis on cancer and inherited disorders.
Genome Explorer® is a Clinical Decision Support System (CDSS) dedicated to the comprehensive analysis of a patient’s whole genome to discover the ultimate genetic cause of disease, and to improve treatment using the most effective drugs. The platform acts as a point of care that satisfies all of the expectations of clinicians and molecular diagnostic specialists.
Genome Explorer is included with platforms such as:
These platforms can also be licensed individually
Learn MoreA user-friendly interface simplifies bottlenecks in clinical reporting. The platform can quickly generate detailed genomic reports that help doctors to decide the precise treatment for their patients. It's designed for genetic testing labs, clinicians and hospitals to reduce their turnaround time for genomic reporting. The platform is designed to provide faster clinical decisions in just a few clicks.
The exploration of population genomics can provide valuable insights into human heritage, migration patterns, and overall health through the examination of genetic profiles. This breakthrough enables us to enhance the accuracy and personalization of disease prediction, diagnosis, and treatment. Furthermore, it plays a critical role in characterizing and prioritizing drug target locations, ultimately leading to the development of novel pharmaceuticals.
Family analysis platform serves as a valuable tool for geneticists, clinicians, and researchers, facilitating the examination of genetic data from multiple family members. It is instrumental in pinpointing the genetic origins of a child's disorder. Additionally, this approach is widely employed to discern hereditary patterns related to both medical and psychological factors that traverse through family lineages.