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Cancer Genetics

ONCOSEQ DNALAB CANCER TYPE-SPECIFIC THERAPEUTIC PANELS

ONCOSEQ DNALAB CANCER TYPE-SPECIFIC THERAPEUTIC PANELS

As DNA Laboratuvarları Genetic Diseases Evaluation Center, the cancer-specific panels we offer are continuously updated to provide our patients with the most appropriate and effective treatment options for each type of cancer. These panels have been carefully developed to ensure that our patients receive targeted treatment according to their individual needs.

  • Report Duration:
    21 Days
  • Sample Type:
    FFPE(Tissue) and Blood (with Edta)

Lung Cancer Panel

Sample Material; FFPE (Tissue) and Blood (with Edta)

Lung cancer occurs when cells in the lungs grow and spread uncontrollably. These abnormal cells become a tumor over time and can damage surrounding tissues.

TYPES:

1.Small Cell Lung Cancer (SCLC): This type is a type of cancer that grows rapidly and tends to spread. It is usually seen in smokers.

2.Non-Small Cell Lung Cancer (NSCLC): It is the most common type and has subtypes such as adenocarcinoma, squamous cell carcinoma and large cell carcinoma. This species generally grows slower.

DNA Image
DNA Image

Genetic factors may influence the risk of lung cancer, but this risk is often compounded by environmental factors (e.g. smoking). Family history and genetic mutations play important roles in assessing personal risk and creating treatment plans. Hereditary or somatic mutations, personalized treatment approaches target these mutations and offer more effective treatment options.

  • EGFR
  • PIK3CA
  • KRAS
  • NRAS
  • BRAF
  • ALK
  • MET
  • ROS1
  • NTRK1
  • NTRK2
  • NTRK3
  • HER2
  • RET
  • PD-L1 (IHC)
  • MSI (STR)

Colorectal Cancer Panel

Sample Material: FFPE (Tissue) and Blood (with EDTA)

Colorectal cancer (CRC) is cancer of the large intestine (colon) and rectum. Genetic factors play an important role in the development of colorectal cancer, and both genetic predisposition and somatic mutations can affect the risk of this disease.

Genetic Predisposition: More frequent and earlier screening is recommended for individuals with family history or genetic risk.
Screening Methods: Early diagnosis can be made using methods such as colonoscopy, sigmoidoscopy and DNA tests.

DNA Image
DNA Image

The genetic underpinnings of colorectal cancer play an important role in determining the risk of this disease and developing personalized treatment approaches. Genetic testing and counseling are valuable tools for understanding risks and taking appropriate precautions.

  • BRAF
  • PIK3CA
  • KRAS
  • NRAS
  • MET
  • HER2
  • PD-L1 (IHC)
  • MSI (STR)

Melanoma Cancer Panel

Sample Material: FFPE (Tissue) and Blood (with EDTA)

Melanoma is a type of cancer that originates from melanocyte cells in the skin. Melanocytes produce melanin, the pigment that gives our skin its color. Melanoma usually begins when moles or congenital pigmented lesions on the skin become malignant.
Genetic testing and counseling helps identify personal risks and take appropriate precautions. Sun protection, regular skin checks and early diagnosis are key elements in effectively managing melanoma.

  • BRAF
  • NRAS
  • cKIT
  • MYC (8q24)
  • MSI (STR)
DNA Image

Stomach Cancer Panel

Sample Material: FFPE (Tissue) and Blood (with EDTA)

Stomach cancer is abnormal and uncontrolled cell growth that occurs in the stomach tissue. Stomach cancer usually begins in the cells on the lining of the stomach and can spread throughout the stomach over time.

Adenocarcinoma:
Most stomach cancers are of this type and consist of glandular cells in the mucosal layer of the stomach.

Other Types:
Rarer types include sarcoma, lymphoma, and cancers that have metastasized to the stomach.

  • BRAF
  • NTRK1
  • NTRK2
  • NTRK3
  • RET
  • HER-2
  • PD-L1 (IHC)
  • MSI (STR)
DNA Image

Discover Your Genetic Heritage

You can contact us to get information about our genetic tests, consultancy services and more.

Contact us

ONCOSEQ DNALAB (Cancer Genetics)

PRIMIS Non-Invasive Prenatal Test

Preimplantation Genetic Diagnosis (PGD)

Whole Exome Sequencing

Clinical Exome Sequencing

Rare Diseases

Carrier Panels - SMARİS