
Onco screen
Cancer is a leading cause of death worldwide, accounting for nearly 10 million deaths in 2020. Each year, approximately 400 000 children develop cancer1
DNA OncoScreen is a comprehensive cancer screening test that helps identify the risk for developing certain types of cancers. It combines genetic risk assessment (<700000 markers across the genome) and biochemical testing to provide an accurate risk assessment for different cancers and known risk factors
Why DNA OncoScreen?
Cancers are most curable in early stages of manifestation. Unfortunately, less than 20% of the cancer patients in India are diagnosed and treated in the early stages. Most cancers in the country are detected at a later stage due to the lack of awareness and screening strategies. Cancer screening can help in early detection, management and potentially, curing cancer.
Conditions covered
Cancers | Traits | BIOCHEMICAL TESTS |
---|---|---|
Colorectal Cancer | Obesity | |
Prostate Cancer (♂) | Prostate Specific Antigen(♂) | CBC - Hb, RBC, Total WBC, MCH, MCV, PCV, MCHC, Differential count |
Lung Cancer | Nicotine Dependence | ESR |
Breast Cancer (♀) | Alcohol Flush Reaction | Beta-HCG |
Bladder Cancer | Antioxidants | CUE |
Melanoma | Alcoholism | AFP |
Hodgkins Lymphoma | CEA | |
Non Hodgkins Lymphoma | Fecal occult blood testing | |
Chronic Lymphocytic Leukemia | CA-125 (♀) | |
Renal Cell Carcinoma | CA - 19.9 | |
Ovarian Cancer(♀) | PSA (♂) | |
Thyroid Cancer | CA-15.3 (♀) | |
Pancreatic Cancer | LDH (♂) | |
Basal Cell Carcinoma | ||
Testicular Cancer (♂) |
You will get to know about
Genomic analysis
BIOCHEMICAL TESTS
Clinical utility
- Comprehensive screening for prevention & early detection of cancers with a combined biochemical & genetic analysis.
- Wide array of blood tumour markers screened.
- DNA mapping across 100+ genes using gold standard technology.
- Genetic counselling and action plan, personalised to YOU.
Test specifications
Technique | Coverage | Variant types | TAT | Sample requirements |
---|---|---|---|---|
NGS | 700 - 800X | SNV | 3 - 4 weeks | 1µg - 2µg of DNA Sample, EDTA Blood (2-3ml), 4-5ml in Sodium Citrate tube, 4-5ml in ACD tube, Urine Sample, Stool sample |