Uses a simple blood draw instead of invasive tissue biopsies.
Detects low levels of circulating tumor DNA with high accuracy.
Profiles hundreds of cancer-related genes for actionable insights.
Delivers results within approximately 7-14 days from sample receipt.
Employs machine learning algorithms to improve data interpretation.
Designed specifically for oncology practice with evidence-based applications.
Available through healthcare providers in multiple countries.
Screen individuals at high risk for cancers like lung or colorectal to detect disease at an early stage.
Identify genomic alterations to choose targeted therapies such as EGFR inhibitors for lung cancer.
Track changes in circulating tumor DNA levels to assess the effectiveness of ongoing therapies.
Monitor patients after treatment to catch recurrence early through regular blood tests.
Match patients to clinical trials based on their genomic profile for innovative treatments.
Use in children for non-invasive cancer diagnosis and monitoring due to minimal sample requirements.
Guide therapy in advanced cancer cases by identifying resistant mutations and new targets.
Serve as a test required for prescribing specific targeted cancer drugs.
Support academic and pharmaceutical research by providing genomic data from patient samples.
Integrate into health check-ups for proactive cancer screening in asymptomatic individuals.
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