Genetic Testing

One of the leading IVF centres in India, Seeds of Innocence has a dedicated genetic testing department that carries out research and testing on the embryos. Equipped with the latest technology and maintained by a well-trained staff, the genetic testing in India helps us immensely in delivering healthy babies and creating happy families. Where the main aim is to fulfil the dream of parenthood for couples, SOI takes pride in having helped more 12,000 couples in the country so far, across 12 centres in 7 states. Genetic testing for infertility plays a huge role in this regard.

Preimplantation Genetic Testing usually involves tests that are performed at various stages, including during IVF, during pregnancy, and other tests to identify and prevent hereditary diseases at any given stage of the treatment. Book an appointment at Seeds of Innocence to know more about what is genetic testing in IVF, healthy sperm diet, prenatal genetic screening, and more.

Genetic Testing During IVF

The sperms and the Egg of a female contain their own genetic material and information that helps in determining the future of the resulting offspring. That is why after egg retrieval and ICSI, a few cells are taken from the embryo so they can be tested by the genetics laboratory. The transfer of the embryo only takes after the results of the genetic test are available. It must be noted that this test does not alter the timeline of the overall treatment.

Here is a nod to all the genetic testing services that we at SOI provide to our patients:

  • PGT-A
    PGT stands for Preimplantation Genetic Testing, while the A in PGT-A stands for “aneuploidies”. In this test, the embryo is tested for all 46 chromosomes for a missing or an extra chromosome, a condition that is called aneuploidy. PGT-A is very useful in testing the most likely embryo for complications that may later develop into conditions like the Down Syndrome.
  • PGT-M
    PGT-M is the condition in which the testing is performed for monogenic or single gene disorders. This testing reduces the risk of the child contracting an inherited diseases caused by the mutation of a single gene, like cystic fibrosis or Huntington’s disease.
  • HLA Matching
    HLA matching is a way to cure a family member of a hereditary disease using the stem cell from a preserved sample of cord blood. HLA or Human Leukocyte Antigen is an important part of our DNA, and thus plays a large role in acceptance of a donor material later in our life. That is why during the IVF cycle, the embryo is tested for an HLA match with the affected family member, and the cord blood sample will then be stored after the birth of the baby.

Genetic Testing During Pregnancy

Seeds of Innocence provides 3 types of genetic testing during pregnancy. The first test is a non-invasive method of identifying any complications with the developing fetus, the second is a tool for identifying the cause of recurring miscariages in women, while the third to understand the effect of recurrent abortions on the health of the woman.

  • Non-Invasive Pre-Natal Testing
    The test screens for the small amount of DNA of the baby that can be found in the mother’s blood. This is an important test to predict and prepare for genetic disorders like Down syndrome.
  • Product of Conception Analysis
    Recurrent abortions can also have their own impact on the current pregnancy. That is why screening is performed to keep a regular check on the development of the baby.
  • Recurrent Abortion
    Recurrent abortions can also have their own impact on the current pregnancy. That is why screening is performed to keep a regular check on the development of the baby.

Identify and Prevent Hereditary Disease

There are a few other tests that are strictly used for only the identification of the hereditary diseases; the conditions that have been passed on from the parent directly to the offspring. These tests are primarily aimed at preventing the same hereditary diseases from coming into the offspring.

  • Mutation Screening
    It is the testing that is done when the genetic disease has previously been identified or has a history in the family. It can identify diseases caused by a fewer number of mutations or nutations in smaller genes.
  • Exome Screening
    This testing is primarily used for unidentified hereditary diseases or for polygenic diseases, conditions that require the interaction of 2 or more genes. Instead of screening and concentrating at a gene or a related small group of genes, this testing analyzes tens of thousands of impotant genes at the same time.
  • Premarital or Preconception Screening
    A screening that helps the couple ensure that their children will not be at the risk of any hereditary or genetic disease before marriage or conception. It can be used as a tool to determine the possibility of a disease in the future child especially if there is a history of the disease. In some cases, the screening is also a precautionary step.


It is of the best ways to not only identify future health of a child, but is also important in understanding the reasons behind infertility, miscarriages, and the overall incidences of congenital diseases.

Chromosome testing is performed to analyse the possibility of a child developing a genetic disorder before conception.

The best time to check for chromosomal abnormalities is during the IVF cycle. In case there is a possibility of a child developing a genetic disorder, it will show up in the reports well before implantation of the embryo.

Yes. Premarital and preconception analysis can act as a great tool to understand how the health of a child will progress as it takes into consideration the history and genes of both, the mother and the father. For more information on this, you and your partner can visit us for a consultation. Book an appointment today.

Heredity or family history is not that big of a factor in a person’s infertility. So to think that infertility is a genetic disorder is wrong as there are several other major factors that may contribute to infertility.