genetics

NIPT – non-invasive prenatal testing

NIPT – non-invasive prenatal test is used to assess the risk of chromosomal aberrations that are the most commonly observed in a fetus. It allows for […]

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Karyotype of a miscarried foetus

Early pregnancy loss is often an effect of embryo genetic abnormalities. These abnormalities may come from parents’ reproductive cells or from mutations occurring during divisions of […]

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Whole gene NGS sequencing

    Test BRCA1 i BRCA2™ The BRCA1 and BRCA2 test is a genetic screening test performed using the Next Generation Diagnosis (NGS) technique. It aims […]

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International Quality Control in Preimplantation Genetic Diagnosis

Since 2013, a new tool in molecular biology – Next Generation Sequencing (NGS) – has been used for preimplantation genetic diagnosis. This technology is used to […]

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PGD TRS™ Pre-implantation diagnosis for translocations

PGD TRS™ preimplantation diagnosis allows examining the cells collected from embryos for the presence of abnormalities resulting from balanced reciprocal translocations in parents. This testing technique […]

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Research and Training Symposium of the Polish Society for Reproductive Medicine 7-8th October, Warsaw

On 7-8 October 2016, INVICTA Research Team will participate in the Research and Training Symposium of the Polish Society for Reproductive Medicine and Embryology and the […]

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NGS technology – the best solution for preimplantation diagnosis of reciprocal translocations

PGD TRS is dedicated to all patients diagnosed with reciprocal translocations i.e., exchanges of genetic material between different  chromosomes. Such mutations are detected by karyotype testing. […]

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5th Polish Genetics Congree

Polish Genetics Congress, organized by the Polish Genetics and Polish Human Genetics Societies ends today. Our research team was among the scientists presenting abstracts during a […]

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PGD testing for reciprocal translocations – now with NGS

PGD TRS is dedicated to all patients who were diagnosed with translocation of fragments of the genetic material between individual chromosomes, namely reciprocal translocations. Such mutations […]

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FertiGenes Test™ – Genetic diagnosis for infertility and recurrent miscarriages

Female Infertility FertiGenes Test™ Female Infertility is a genetic test for women planning a pregnancy. It has been designed for couples seeking to become parents. The […]

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PGD: genetic pre-implantation diagnostics – facts and myths

Thanks to advances in medical science we have now diagnostic tests that can be used at the very beginning of human development. It is now possible […]

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PGD ONE FM™ – Preimplantation Diagnosis for Monogenic Diseases – most Frequent Mutations

PGD ONE FM™ is a test that detects the genetic defects (most frequent mutations) inherited by a child from their parents. DNA material from embryos is […]

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Sex-linked diseases

Inheritance of some genetic diseases is linked to a sex chromosome. These disorders are also called sex-linked diseases. Approximately 800 various genes were identified on the […]

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Polish Leader in Genetic Diagnosis for Reproductive Medicine at ESHRE 2016

32nd Annual Meeting of the European Society of Human Reproduction and Embryology (ESHRE) is over! During the event held between July 3 and 6 in Helsinki, […]

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