Proprietary Program Classifies Broader Range of Cancer Risk Genes
A history-weighting algorithm has been shown to upgrade and downgrade variants of uncertain significance to more definitive clinical classifications, with high accuracy.
Read MoreSearch Results for: genetic testing
Variant Scoring and Classification Module Supports Clinical NGS Report Consistency
The functionality provides an intuitive interface and workflow for labs to systematically assess the disease-causing potential of genetic variants using clinical guidelines.
Read More
The Value of Diagnostics
The conclusion to our three-part series exploring the value of diagnostics.
Read MorePartners Connect to Examine Asian-Specific Genetic Mutations in Cancer
Singapore General Hospital and Thermo Fisher Scientific are collaborating to study the mutational profiles of cancer patients with Asian ancestry.
Read MoreStudy Yields Positive Results for Noninvasive Prenatal Test
In a clinical validation study, Sequenom’s laboratory-developed noninvasive prenatal test was shown to exhibit high resolution, sensitivity, and specificity.
Read More