Clinical Genomics cloud Platforms for Genetic Laboratories, Hospitals, Pharmaceutical Companies, and genome research Institution's.
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.
Clinical Decision Support System (CDSS)
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.
- Empowered with a variety of molecular diagnostic and genetic risk tests in multiple verticals, with its actionable mutation data for disease and therapeutics, as well as its unique predictive capabilities.
- Innovative, cost-effective, and readily accessible Clinical Decision Support System at your point of care, that manages all patient data and reports in your EHR.
Genome Explorer is included with platforms such as:
- Genomic Clinical Reporting (GCR)
- Cohort Genomics
- Family Genomics
These platforms can also be licensed individually
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Clinical Genome Analysis and Reporting Platform
A 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.
- Simplified and detailed genomic reports.
- Adheres to industry-standard clinical guidelines and produces accurate and precise reports.
- Customized for genomic laboratories and hospitals.
- Facilitates personalized medicine by identifying tailored treatment options.
Population Genomics Platform
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.
- Allows researchers to analyze and interpret large datasets of genomic data from multiple individuals as a cohort.
- Hosts a variety of features for data preprocessing, analysis, and visualization.
- Powerful tools for analyzing and interpreting large genomic datasets.
- Can be used to identify and interpret genetic variants associated with disease or other traits.
Family Analysis Platform
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.
- The platform is designed to make it easy for geneticists and clinicians to analyze genetic data from members of a family.
- Can be used to identify both inherited and de novo mutations.
- Provides informed treatment decisions.
- Helps a genetic counselor clearly explain the facts to the family.