Our Technology


Applying the possibilities and innovation that genetics brings in medicine requires high technology.

We, at Nesiller Genetik, give higher importance to technology and innovation, we follow the most recent technological developments, use and invest in them in accordance with our target to raise our service quality consistently.

In addition, by using high-tech devices and materials in our laboratories, we carry out R&D activities and examinations in accordance with our principle to prioritise technology and innovation.

We use state of the art technology in our center using devices such as Miseq and PGM new generation sequencing devices and Wafergen automated liquid handling instrument dedicated to the preparation of sample libraries for Next-Generation Sequencing.

Technology Leadership

Thanks to our high-technology laboratory, we are able to open new doors for detecting, preventing and treating diseases.

Nesiller Genetik R&D department always works actively for new and innovative diagnostic tools that help health service providers with early diagnosis and disease management. Our cutting-edge technology combined with highly trained staff ensures meeting the experience requirement of most medical branches.

To transform our solutions into products is also a target for us. In this direction, we carried out 3 different projects with the support of the Scientific and Technological Research Council of Turkey (TÜBİTAK)

  • Beta Thalassemia (Mediterranean Anemia) Diagnosis Test in Preimplantation Genetic Diagnosis

We developed this test kit with the Scientific and Technological Research Council of Turkey. The kit aims to scan genetic disorders causing this condition which is frequently seen in our region.

  • Fetal Rh Factor Detection with NIPD

Nowadays, there is no need to apply invasive methods to understand the chromosomal structure of the foetus. We developed a kit aiming to detect the Rh factor which causes blood incompatibility in the 6th week of pregnancy. Our purpose is to give MDs the opportunity to solve the problems that may occur during pregnancy by providing the information at early stages.

  • CML diagnosis and treatment follow-up, BCR/ABL fusion protein

We developed this kit focusing on genetic scanning devoted to Chronic Myeloid Leukemia (CML) diagnosis and treatment follow-up.

In addition, all our operations are integrated into a modern IT system because it is very important to us to analyse, assess and report well all operations and processes holding value element in the foreground in order to keep sustainable growth and competitiveness.

Thanks to these qualities, our laboratory has become one of the most developed and high-quality laboratories for many international labs and MDs.

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