That’s why we launched ADVANCE®, a clinical decision support platform that is transforming genetic and clinical data into new insights for the diagnosis and management of complex health conditions. ADVANCE simplifies diagnosis and informs more accurate management strategies at the earliest signs of pancreatic diseases.
ADVANCE integrates an individual’s genetics, environment, and family and medical history to provide clinicians with more actionable insights into complex diseases, including evidence-based knowledge for management and treatment options. Our AI powered technology combines deep genetic sequencing with advanced analytics and evidence-based knowledge to provide genetic testing and a report that is actionable and easy to use.
Ariel goes beyond genetics to help doctors better identify and treat patients with pancreatitis.
Most patients with a complex, chronic disorder, such as pancreatitis, don’t have a single cause for their disease. Each patient has a unique combination of genetic and environmental risk factors.
Our AI powered technology combines deep genetic sequencing with advanced analytics and evidence-based knowledge to provide genetic testing and a report that is actionable and easy to use.
Ariel analyzes a patient’s genetic data and integrates the patient’s medical history and current symptoms to provide a comprehensive view of the factors that may be contributing to current symptoms.
Ariel’s genetic reporting provides genetic, biological markers along with evidence-based guidelines that are individualized to each patient.
Next-generation sequencing beyond traditional Mendelian variants to detect complex genetic variants for comprehensive risk assessment.
Reports tailored to each patient, integrating genetics, symptoms, hereditary, medical history and environmental factors.
Curated clinical considerations based on up-to-date literature and guidelines for easier, more actionable treatment planning.
Our laboratory is CLIA-certified and offers read depths that far exceed clinical decision thresholds.
Integrates a patient’s symptoms and genetics with medical information and curated evidence-based clinical considerations.
Pre- and/or post-test genetic counseling if you need extra help with genetic testing.
Analyzes multiple risk factors that are disease causing rather than just assessing single gene risk factors.
Order and review test results, add medical team and request patient consent using our portal.
Gain a better understanding of unknown risk factors and whether you have a genetic cause for your condition, or an increased genetic susceptibility to it.
Comprehensive genetic testing and pre- and/or post-test genetic counseling.
Timely diagnosis can prevent costly and invasive diagnostic procedures, and allow for intervention prior to reaching end-stage disease.
Easy-to-use & non-invasive saliva based DNA collection is done at home and then sent to our lab for analysis.
You don’t have to be an expert in genetics.
We help you translate complex genetics data into a more personalized care plan. So, you can focus on optimal care instead of sifting through complicated genetics information.