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What is genetic testing?

Genes are located on chromosomes in the form of small threadlike structures. In normal cases, there are 46 chromosomes in each cell. 23 of these chromosomes come from the mother 23 of them. In some special cases, a mutation may occur that prevents it from functioning correctly during gene copying. Mutation can be the cause of a genetic disorder. A blood or tissue test for identification of changes to chromosomes or gingiva is defined as a genetic test.

What is Informed Consent?

Genes are located on chromosomes in the form of small threadlike structures. In normal cases, there are 46 chromosomes in each cell. 23 of these chromosomes come from the mother 23 of them. In some special cases, a mutation may occur that prevents it from functioning correctly during gene copying. Mutation can be the cause of a genetic disorder. A blood or tissue test for identification of changes to chromosomes or gingiva is defined as a genetic test.

What are genetic testing types?

Genes are located on chromosomes in the form of small threadlike structures. In normal cases, there are 46 chromosomes in each cell. 23 of these chromosomes come from the mother 23 of them. In some special cases, a mutation may occur that prevents it from functioning correctly during gene copying. Mutation can be the cause of a genetic disorder. A blood or tissue test for identification of changes to chromosomes or gingiva is defined as a genetic test.

Welcome to Next Genetic Center

Having a new name is just the beginning.

Nowadays, as the developments in Genetic Science are proceeding at a dizzying pace, our center has been designed and constructed in the light of these innovations brought about by our century. In our center, by examining our samples with the latest technologies in the field of genetics, we give the patient and the physician the most accurate result in the fastest time Our center communicates with the academic staff not only through the sample, but also with the patient himself and the physician who sends the sample, providing solutions supporting diagnose and treatment. At this point, our medical genetic physicians serving in our center, Assoc. Emre TEPELİ and Assoc. Ahmet ULUDAĞ is evaluated by our patients center and detailed individual genetic counseling service is offered free of charge. Who Is Scared of Genetics Both patients and clinicians often suffer from the complexity of their genetics. Rapidly expanding genetic testing, the place of genetics in the changing clinical diagnosis algorithms, and individual genetic diagnosis can be the cause of this complexity. For this reason our center offers clinic-specific genetic solutions. With the common algorithms to be determined, the patient is most likely to be diagnosed correctly. Our specialist team is ready to communicate with you 24/7. There Is No Disease But Patient This motto is one of the most emphasized points in lessons in medicine faculty. Developing individual-specific diagnosis and treatment is accepted today as a countervailing measure. In our genetic codes, this shows the correctness. For this reason, the results of the tests performed at our center are not in the form of reports compiled from the device outputs, but consist of epicrisis assessed by the patients’ clinic.

About Us

NGC Popular Tests

Genetic Counseling

Genetic counseling is a type of service that provides information to individuals and relatives who carry or are at risk of having a hereditary disease, about the illness, treatment methods, recurrence risks, and preventive treatments.

DNA Testing in Maternal Blood

DNA testing during pregnancy was not possible; scientists have succeeded in reaching this information by identifying them from the blood of pregnant women. The diagnostic test used to give information about the general condition of the baby gives the impression that "amniocentesis" has features that frighten the ladies. But Dna carries no risk of smelling in this comparison.

Mikrobiyota

Bağırsak florasının yani mikrobiyotanın ayrıntılı analiziyle oldukça değerli sonuçlar elde edilmektedir. Bu elde edilen bulgular ile obezite, bağırsak hastalıkları, kolon kanseri, artrit, otizm, alzheimer gibi ciddi hastalıkların tanısı ve tedavisinde önemli bir role sahiptir.

Sports Genetics

Gen yapısının analiz edilmesi bireyin kas yapısı ve kardiyovasküler kapasitesi ile ilgili ciddi ipuçlarını elde edilmesini sağlar. Bu sayede kişi kalıtsal genetik yapısı doğrultusunda kendisine en uygun spor dalını seçerek başarı olasılığını en üst seviyeye çıkartmış olur.

Gene Test

The process of examining chromosomes, genes on chromosomes, gene segments or gene products, which contain all the information necessary for the function of the body to be visible, is called "gene testing".

Genetic Test

It is a test for identification of a change in a particular gene or chromosome, if any. In this way mutated gene or chromosome can be detected and observed, and prevention and treatment can be done.

Nutrition Genetics

Belirli bir gen ya da kromozomda meydana gelmiş bir değişim varsa bunun tanımlanması için yapılan testtir. Bu sayede mutasyonlu gen veya kromozom tespit edilerek gözlem altına alınabilir, önlem ve tedavide yol kat edilebilir. Beslenme genetiği testi ile besinlerden maksimum yarar ve minimum zarar adına bir yol haritası çıkartılabilir.

Cancer Test

Cancer diagnostic tests show differences according to the region to be detected. The primary goal in these tests is early recognition before the disease develops. This is to ensure that the quality of life is maintained at the maximum level by passing the cancerous cells that start to occur on this count

News

New Generation Approach to Cancer

One of the most important health problems of our age is cancer. The most important thing to know about cancer is that cancer is a genetic disease. Here, genetics and inheritance should be separated. A disease may be genetic, but it may not be transmitted to other generations. This is the case in cancer. Not all cancers are inherited, but all cancers result from genetic changes. For this reason genetic analysis is of great importance in the identification of diagnosis and treatment. For this reason, cancer genetics is one of the most important issues. With the new generation of genetic technologies and methods it is now possible to arrest cancer early. There are 2 important points in cancer genetics. The primary is to screen for large-scale cancer-related genes by evaluating existing risks (such as age, sex, family history, habits) while not in any clinical setting. These scans can be done at our headquarters using new generation technologies. The risk of cancer can be better predicted by genetic testing. This allows you to make decisions about targeted prevention programs, make informed medical and lifestyle decisions, and also provide useful information about individual risks to other family members. Another point is the molecular diagnosis of cancer after cancer diagnosis. This point is very important. In the definition of cancer treatment for today, these molecular changes are indispensable for effective treatment. One of the most important diagnostic methods of the last period is liquid biopsy. Liquid biopsy is a simple, non-invasive alternative to surgical biopsies that allows physicians to discover a range of information about a tumor through a simple blood sample. Here, the molecular changes of the present cancer seen in the person are made not from invasive tumor tissue or biopsy material, but from the patient blood sample. The advantage of this method is that the cancer can be detected at an early stage and the cancer can be made to follow the recurrence. However, the ability to detect cancer-specific markers even in lesions that are too small to be recognized by other available methods due to liquid biopsy suggests that this method will be one of the important techniques in early detection of cancer.

Patient Acceptance Begins

Today, as the developments in Genetic Science are proceeding at a dizzying pace, these innovations brought about by our century have been designed and constructed in the light. In our center, by examining our samples with the latest technologies in the field of genetics, we give the patient and the medicine the most accurate result in the fastest time. Our center communicates with the academic staff not only through the sample, but also with the patient himself and the physician who sends the sample, providing diagnostic and therapeutic support solutions. At this point, our medical genetic physician who works in our center, Assoc. Dr. Emre TEPELİ and Assoc. Dr. Ahmet ULUDAĞ is presented with detailed individual genetic counseling services in patients' clinics. Kim Korkar Genetikten; Patients, clinicians, often suffer from the complexity of their genetics. Rapidly expanding genetic testing, the place of genetics in the changing clinical diagnostic algorithms, and the genetic diagnosis specific to the individual can be the cause of this complexity. For this reason our center offers clinic-specific genetic solutions. With the common algorithms to be determined, the patient is most likely to be diagnosed correctly. Our specialist team is ready to communicate with you 24/7.

Ekzom Sekanslama

DNA Sequencing (sequencing) is the name given to the method by which the building blocks, called the nucleotides that make up the DNA code of the individual, are examined. Our genes are made up of these nucleotides and all the genetic code we have is called the genome. The DNA sequences that allow the formation of proteins in the genome are called exosomes. The exom (protein coding region of the human genome) represents more than 2% of the genome, but known variants of the disease