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LifeCode Laboratory

Ukraine, Kyiv

LifeCode has been developing in the field of medicine, pharmacology and cosmetology since 2009. Since 2016, the company has focused on its core specialization – genetic research using Next Generation Sequencing (NGS).

Starting with research in the field of reproductive medicine, since 2020 LifeCode has focused on NGS testing in the field of oncology, becoming the first laboratory to introduce this research method in Ukraine.

Next-generation sequencing is an integral part of the future of personalized medicine. Genetic testing of tumors allows doctors to prescribe more effective treatment and predict its outcome.

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    Procedures and their cost

    Recently, in the LifeCode laboratory, the BRCA Plus (4 genes) and OncoRisk (37 genes) studies were replaced with new panels with a specially selected optimal set of genes for each cancer. Now each patient will be able to receive the most relevant information regarding the hereditary predisposition / nature of a certain type of cancer.

    from $685 OncoRisk Complete – extended panel for hereditary cancers (88 genes) from $327 OncoRisk BRCA Plus – Hereditary Breast and Ovarian Cancer Panel (14 genes)
    from $385 OncoRisk Prostate - Hereditary Prostate Cancer Panel (15 genes) from $327 OncoRisk Pancreas - Hereditary Pancreatic Cancer Panel (20 genes)
    from $412 OncoRisk Colorectal - Hereditary Colorectal Cancer Panel (19 genes) from $244 OncoRisk Lynch - Diagnosis of Lynch syndrome (5 genes)
    from $412 OncoRisk GIST - Hereditary Gastric Cancer and GIST Panel (18 genes) from $327 OncoRisk Melanoma - Panel of hereditary forms of melanoma (9 genes)
    from $412 OncoRisk Renis - Hereditary Kidney Cancer Panel (25 genes) from $412 OncoRisk Sarcoma - Hereditary Sarcoma Panel (27 genes)
    from $327 OncoRisk Thyroid - Hereditary Thyroid Cancer Panel (8 genes) from $412 OncoRisk Pediatric - Pediatric Solid Tumor Panel (51 genes)
    from $244 OncoRisk Neuroblastoma - Diagnosis of familial neuroblastoma from $327 OncoRisk MEN1 - Diagnosis of multiple neuroendocrine neoplasia type 1 (1 gene)
    from $327 OncoRisk RET - Diagnosis of multiple neuroendocrine neoplasia type 2 (1 gene) from $412 OncoRisk Blood - Hereditary MDS and Leukemia Panel (15 genes)

    LifeCode Laboratory is a leader in NGS research in Ukraine

    In 2022, LifeCode significantly expanded the range of its services and, thanks to additional equipment of the laboratory and successful cooperation with trusted partners, received the status of a full-cycle laboratory for oncology. Currently, LifeCode employees work with NGS, immunohistochemistry and PCR methods, covering a wide range of necessary studies for all types of cancer. They carry out both single-gene PCR tests and small NGS panels, as well as full molecular profiling for 500+ genes.

    LifeCode’s team of employees are professionals with many years of experience in areas such as biotechnology, oncogenetics, molecular pathology and clinical oncology. They are united by a common goal – to improve the quality of diagnosis and treatment of cancer patients in Ukraine with the help of modern technologies and developments in the field of genetics.

    LifeCode Laboratory equipment

    The main apparatus, the heart of the LifeCode laboratory, is the new generation sequencer Ion Proton System, manufactured by ThermoFisher Scientific (USA). This is a platform for performing NGS research that provides efficient sequencing of DNA and RNA molecules. Thanks to innovative simultaneous multiple reading technology, studies are carried out quickly and with a high level of accuracy.

    Laboratory staff use only high-quality and proven reagents produced by companies from the USA, Australia and Great Britain, which are used by leading genetic laboratories around the world. In addition, the laboratory is equipped with ultra-modern equipment, thanks to which most processes are performed automatically. This significantly reduces the risk of human error and ensures consistently high-quality research results. LifeCode collaborates with leading oncology specialists, establishing itself as a trusted laboratory.

    LifeCode секвенирование нового поколения

    What is next generation sequencing and what is this research for?

    Over the past 10 years, DNA sequencing has transformed from a niche field pursued by a small group of scientists to a rapidly evolving technology. New generation sequencers have become noticeably cheaper and much more efficient than their predecessors. The development of sequencing has revolutionized bioinformatics and biology, and is already rapidly moving forward, significantly changing medicine.

    NGS for selection of effective anticancer therapy

    New methods and diagnostic capabilities in the field of cancer genetics have made it possible to establish that each tumor has its own unique characteristics. No two cancers are the same. Even neoplasms located in the same place are heterogeneous in their composition and origin, and therefore respond differently to treatment.

    These differences have become the basis for the development of pharmacological drugs that act directly on the molecular target in the tumor cell, without affecting other organs and tissues of the patient.

    The peculiarity of such targeted therapy is that each drug is effective only for tumors that have certain molecular characteristics. Therefore, the use of most targeted drugs requires mandatory identification of genetic disorders.

    Thus, the results of DNA sequencing of patients make it possible to identify mutations in tumor genes that are targets for targeted drugs. This helps the doctor select highly effective personalized therapy.

    NGS as a method of cancer prevention

    Next-generation sequencing makes it possible to identify certain mutations that increase the risk of developing cancer. Patients who carry these mutations should undergo regular screening for early detection of cancerous tumors. Timely detection of mutations makes it possible to predict the development of cancer, select a personalized therapeutic strategy, prevent recurrent disease and, finally, prevent serious consequences for the patient.

    The MedTour platform cooperates with the best medical companies in the world that are engaged in the development and implementation of innovative technologies, such as the LifeCode laboratory. If you are interested in identifying gene mutations that increase the risk of developing cancer, or you need to create a “genetic portrait” of a tumor in order to select the most effective treatment, call or write to us. The MedTour coordinator will provide all the necessary information and help organize the diagnostic process.

    Services provided by the clinic LifeCode Laboratory

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    Location LifeCode Laboratory
    Ukraine, 03680, Kyiv, Antonovycha st., 68

    Frequently Asked Questions

    1
    What is NGS tumor molecular profiling in simple words?

    Next-generation sequencing (NGS) is a special type of molecular profiling that can test a single tumor sample for hundreds of gene changes or defects at once.

    1
    What are the benefits of next generation sequencing (NGS)?

    Compared to traditional methods, NGS is a more accurate and faster study. Because this technology makes it possible to evaluate multiple genes in one test, a patient does not need to order multiple tests to determine the causative mutation. This multigene approach reduces wait times for results and does not require the provision of multiple tumor samples at once. In addition, NGS has very high sensitivity, allowing it to detect mutations present in as little as 5% of the DNA isolated from a tumor sample.

    1
    What information does the NGS examination provide?

    Next-generation sequencing (NGS) helps doctors pinpoint genetic mutations in a tumor and predict a patient’s response to various treatments. NGS compares tumor genes with genes in a normal or reference genome. Once genetic changes are detected, the doctor can select drugs that target these mutations directly and do not affect healthy cells in the body.

    1
    How does NGS research help in cancer?

    Understanding the biology of a tumor not only helps doctors determine the best therapy for a patient, but also helps determine how aggressive the treatment strategy should be. Information obtained using NGS makes it possible to determine the patient’s prognosis and helps in choosing an antitumor technique that may be less harmful than standard chemotherapy and radiation therapy. Treatments that target specific genetic mutations are believed to increase survival and improve patients’ quality of life.

    1
    How much does tumor genetic profiling cost?

    You can see the prices for genetic tests in the table on our website or check with the MedTour coordinating doctor by phone.

    1
    I was diagnosed with mutations in my genes. Does this mean I will get cancer?

    No. Inheriting a gene mutation means you have an increased risk of developing cancer, but does not necessarily mean you will get it in your lifetime. If the test result is positive, you will be advised to undergo preventive examinations more often. For example, if you have a change in the BRCA gene that increases your chance of developing breast cancer, your doctor will advise you to get mammograms starting at an earlier age or more often than patients who are not at high risk.

    Published:

    Updated:

    Olena Kursabaieva
    Medical author, Medical editor:
    Natalia Segen
    Medical author, Medical editor: