NGS – WHAT IS NEXT GENERATION SECUENS?

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    Kapsamlı Kromozom Taraması

    Ngs is the genetic analysis technology used in comprehensive chromosome screening. Also called next-generation sequencing. With the in vitro fertilization ngs method, the embryo is scanned quickly and comprehensively before transfer. During the screening, it is checked whether there is a genetic problem or damage at the chromosome level. If there is a genetic problem, the embryo is detected before transfer. Because if there is a chromosomal disorder in the embryos, the treatment will not result in a healthy pregnancy. Healthy embryos are selected because all 24 chromosomes are extensively screened with Ngs genetic screening. Those who have IVF with Ngs have an increased chance of healthy pregnancy.

    Who is NGS Applied to?

    • In recurrent miscarriages,
    • In expectant mothers over the age of 38,
    • In severe male infertility,
    • In cases of unknown infertility,
    • It is applied in recurrent treatment failures.

    What are the Features of NGS Technique?

    With the ngs method in IVF, numerical and structural problems of chromosomes in cells are determined comprehensively and accurately.

    Embryos containing two or more cell aggregates with different chromosomal structures are called “mosaic embryos”. Mosaic embryos are more easily identified with the NGS technique.

    With Ngs, gene disorders and chromosomal errors are detected at a sensitive level. For this reason, it allows comprehensive chromosomal screening simultaneously with HLA typing.

    What is the NGS Test Price?

    NGS test price is 350$ per embryos

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