Using the most advanced equipment, it is possible to isolate a human chain of DNA and RNA, determine the sequence of its constituent links - nucleotides - and the mutations that occur in it.

Genetic material extracted directly from cancer cells is tested for the presence of different types of mutations, which is important for cancer patients planning to start treatment.

Taking individual mutations into account enables targeted medication selection, making the treatment process more effective and more personalised. 

The types of mutations that can be tested are as follows:

Colorectal Cancer Mutation Panel

• KRAS
• NRAS
• BRAF
• PIK3CA
• AKT 1

Lung Cancer Mutation Panel:

• ALK
• ROS
• RET
• MET                                                                                                                                       
• EGFR

BRAF gene mutation

IDH ½ (isocitrate dehydrogenase ½)

DPYD 2A polymorphism to determine sensitivity to chemotherapy

Instability of MSI microsatellites 

Hereditary predisposition to various diseases is well known, and the same is true for oncological processes. Oncogenetic studies make possible the determination of the genetic genesis of diseases such as colorectal cancer, prostate cancer, breast cancer, ovarian cancer, endometrial cancer and pancreatic cancer.

Testing for mutations in the BRCA1/2 genes is essential.

Testing is recommended for individuals with a strong family history (two or more cases of cancer in first- or second-degree relatives) and for patients with a strong personal history (cancer diagnosed before the age of 50, ovarian and breast cancer at the same time, cancer with metastatic lesions).

The 8 major mutations in the BRCA1/2 genes account for 98% of all mutations in these genes. The test is performed both in the blood to detect an inherited tumor and in tumour cells to determine the course of treatment. 

Lifestyle adjustments and regular screening can therefore not only diagnose various types of cancer at an early stage, prevent neglected cases and associated complications, and provide effective treatment, but also in some cases prevent the diseases themselves.

The laboratory also studies the presence of a tendency to thrombosis, which is important for patients with cardiovascular diseases. Due to the severity of its consequences, thrombophilia plays an important role in obstetric and reproductive practice

Of the many known genetic factors that cause thrombophilia, the following genetic disorders have been confirmed and recommended for testing

• FV Leiden mutation
• FII Prothrombine mutation
• PAI-1 4G/5G mutation
• MTHFR C677T mutation
• MTHFR A1298C mutation

The Molecular Diagnostics Department can also detect sexually transmitted infections with 12 different genotypes using the polymerase chain reaction method, including:

• Mycoplasma Genitalium
• Mycoplasma Hominis
• Ureaplasma Urealyticum
• Ureaplasma Parvum
• Neiseria Gonorrheae
• Gardnerella Vaginalis
• Treponema Pallidum
• Trichomonas Vaginalis
• Chlamydia Trachomatis
• Herpes Simplex Virus type-1
• Herpes Simplex Virus type-2
• Trichomonas Vaginalis

In addition, high oncogenic risk papillomavirus genotypes are also determined.