Our proprietary integrated solution helps maximize response to therapy by evaluating both germline variants and somatic mutations to inform therapy decisions across the patient journey.
Next-generation sequencing (NGS) evaluates the tumor’s DNA via a biopsy sample, analyzing somatic mutations for key characteristics.
Pharmacogenomics testing (PGx), via a buccal swab, establishes a clear understanding of the patient’s potential drug/gene and drug/drug interaction by analyzing germline variants.
*NGS and PGx are also available separately.