NGS (Next Generation Sequencing Technique) Against Genetic Failures

NGS technology, which provides a detailed and rapid examination of the embryo, enables the identification of embryos with no chromosomal abnormalities and the highest pregnancy-forming capacity. NGS, which allows all chromosomes to be examined, aims to ensure that the embryo is attached to the uterus.

NGS technology is especially recommended for male infertility, infertility of unknown cause, recurrent miscarriages, repeated failed IVF attempts and advanced age patients.

NGS is a genetic analysis technology that enables comprehensive chromosome screening of embryos. With NGS, embryos are screened quickly and effectively and genetic problems at the chromosome level can be detected before pregnancy. Chromosomal abnormalities in embryos are one of the most important reasons for the failure to achieve a healthy pregnancy despite the successful transfer of embryos to the uterus in IVF treatments. Detailed chromosomal screening using the NGS method plays an active role in detecting chromosomal abnormalities in embryos. Especially in patients with recurrent miscarriages and candidates who want to have a baby over the age of 40, treatments are carried out by transferring the embryo, which is determined to be chromosomally healthy by the NGS method, to the uterus.