Turnaround Time (TAT): 15 business days | Genes: 118
Purpose:
The most comprehensive cancer genetic panel, covering a broad range of cancer-associated genes. The panel is carefully curated based on their proven risk involvement in the development of multiple cancers, including breast, ovarian, colorectal, gastric, thyroid, endometrial, pancreatic, melanoma, renal, and prostate cancers, among others.
Method:
Next-Generation Sequencing (NGS) including CNV analysis | Coverage: ≥99% at ≥20×
Sample Required:
EDTA blood sample – 5 ml
Key Benefits:
• Provides the most comprehensive hereditary cancer risk assessment
• Maximizes diagnostic yield and clinical utility
Who Is This Test For?
• Patients starting or adjusting cancer treatment
• Individuals receiving systemic cancer therapies
• Patients in remission requiring longitudinal follow-up
• Patients for whom tissue biopsy is not feasible
• Metastatic cancer patients requiring regular monitoring
• Identifies inherited genetic variants that may increase the risk of developing certain cancers
• Provides valuable insights for both patients and their families
• Supports earlier detection and proactive health monitoring
• Enables personalised screening, prevention, and follow-up strategies
• Uses advanced Next-Generation Sequencing (NGS) technology to analyse multiple cancer-related genes simultaneously
• Helps patients and clinicians make clearer, more informed healthcare decisions
• Identifies inherited genetic variants associated with Parkinson’s disease and different forms of dementia
• Supports earlier diagnosis and improved risk assessment
• Helps guide personalised treatment, follow-up, and long-term care strategies
• Valuable for patients with symptoms or a family history of neurological disorders
• Based on advanced Next-Generation Sequencing (NGS) technology
Cancer is a ticking time bomb globally. Every year about 18 million women and men are diagnosed with various cancers including carcinomas, sarcomas, neuroendocrine tumors, melanomas. These cancers are also associated with about 9 million deaths. This translates into roughly 34 cancer cases being detected and 18 cancer related deaths every minute. Annually, these cancers contribute to:
CANCER CHECK IS A BLOOD TEST THAT CAN ENABLE EARLY DETECTION OF MULTIPLE CANCERS IN ASYMPTOMATIC INDIVIDUALS.

It detects ‘existence of cancer’
Cancer Check is not intended to be and should not be considered as a replacement for any Stan- dard of Care screening tests.
Within the limits of error, a ‘negative’ result is a reasonable indication of undetectable cancer of the type covered by the test. For other cancers not covered by the test, no inference should be drawn from a ‘negative’ result.
A ‘negative’ results means that at the time of the test there were no detectable cancer cells circulating in the blood.
As Cancer Check is a non-invasive blood test, there is no disadvantage in frequent testing. However, we advise that Cancer Check should be performed every 12 months in case of every negative result.
The test indicates the location for the select types of cancers with high accuracy, and in others the Tissue of Origin can be identified with reasonable accuracy. In all cases of ‘positive’ results, the Report should be interpreted by your physician who can guide you on further course of action.
No, such individuals should seek expert medical advice without delay.