Sunshine provides efficient genetic screening in the form of PGS (Preimplantation Genetic Screening) and NGS (Next-Generation Sequencing) programs. These tests help clients to make sure their family complement will be successful and without any possible genetic pathologies. Generally speaking, proper NGS analysis and PGS testing provided by qualified specialists will undermine all risks when you are going to have a baby with the help of reproductive medicine, in particular, with in vitro fertilization and will increase the pregnancy success rate.
Well, the thing is that if any errors occur during germ cells formation or merging, the born individual may have serious deviations or problems during the one’s further reproduction. Fortunately, contemporary medical technologies can help to prevent all these issues and so to minimize risks of disabled children birth. Genetic screening in a form of NGS analysis and PGS comes as a number-one method for detecting possible abnormalities at the genetic level. Sunshine fertility experts will gladly provide you with high-quality assistance and support during the whole testing process.
Basically, the PGS is a medical procedure used to assess the state of an embryo’s chromosomes. The results of this test help doctors decide whether the embryo is suitable for conception. Based on PGS results, the healthiest and potentially most productive embryo can be selected based on an analysis of chromosomal deficiencies. The most prominent deficiency detected by preimplantation genetic screening is called aneuploidy.
Aneuploidy describes embryos which have one too little or one too many chromosomes. Aneuploid embryos also can be selected for the transfer to the uterus because they look the same as the ones without any pathology. After the transfer of this kind of embryos, there still might be no pregnancy or a miscarriage may occur on an early stage. Moreover, aneuploidy may cause the birth of a child with disease marked by mental or physical retardation. With the PGS testing results, specialists can detect aneuploidy and prevent the transfer of the aneuploid embryo to the uterus and so to minimize the risk of birth of a child with deviations.
If you want to make sure the embryo has no genetic abnormalities, you definitely have to go through the test to get PGS results. However, there are some vital reasons to apply for this method, and they include:
When it comes to the genetic screening, it is crucial to pick a method that perfectly fits your situation. Sunshine offers a full NGS analysis which is the most innovative method of preimplantation genetic diagnosis. Thanks to its effectiveness and high accuracy, next-generation sequencing allows medical staff to avoid misleading results and has recently been replacing other possible methods worldwide. Additionally, NGS program is safe for the embryo as it allows to handle the biopsy starting from the fifth day of embryo development when the one already contains a required number of cells.
Being the advanced and the most up-to-date method of genetic screening, NGS is based on the determination of DNA sequencing. This is what makes NGS analysis stand out among other techniques. Well, NGS is a sensitive way of screening that allows experts to detect such an essential thing as mosaicism. Basically, mosaicism means the presence of cells with diverse sets of chromosomes. If the particular embryo has this issue, it may cause a pregnancy miscarriage or the birth of a child with a dangerous pathology that may affect the one’s life. NGS helps to detect the mosaicism on the pre-implantation stage. Moreover, it allows specialists to choose only genetically-healthy embryos for a further transfer and increases the level of successful gestation in general.
We at Sunshine serve you with the latest methods and solutions and try to do our best to help you enjoy the birth of a healthy baby.
NGS analysis is helpful if you want to prevent any possible issues with the health of your future baby. We highly recommend you to apply for this genetic screening method in case:
Sunshine egg donation agency aims at providing the best services for our intended parents, so we are always keeping up with the most recent advances in medical science and technology.
If there is still something unknown for you concerning the most effective genetic screening methods that Sunshine provides, please, take a look at the section of frequently asked questions.
PGS is a reliable way to maximize the chances of a successful conception. It allows fertility experts to detect the most promising embryos to use for the transfer. We use the most advanced techniques – PGS and embryo biopsy – to improve our patients’ chances of getting pregnant by over 25%. Do not confuse PGS with Preimplantation Genetic Diagnosis (also referred to as PGD), as PGS won’t be able to detect certain inherited genetic defects in the examined embryos. Instead of that, PGS is aimed at finding anomalies in the number of chromosomes (aneuploidy). On the other hand, PGD can detect the following genetic defects:
● cystic fibrosis
● sickle cell anemia
These defects have a significant impact on the embryo’s genetic potential, so it is crucial to detect them early on and prevent the embryo from being further used.
We recommend women over 35 years old to go through the preimplantation genetic screening to successfully detect possible defects in chromosomes. This is a good idea because patients in advanced maternal age are more likely to have low-quality eggs due to biological and hormonal changes. We also highly recommend PGS for every woman who is going to use IVF. The main benefit of PGS is that it allows experts to learn more about all embryos that are going to be used for pregnancy attempts. That way, the best embryos can be chosen and the optimal fertility treatment plans can be worked out. However, PGS is a rather expensive procedure, and its results may be erratic (1.5% chance).
PGS allows to obtain a single cell from any given embryo and analyze it to detect specimens of sub-par quality. Rest assured that the cell biopsy procedure is not harmful to the embryo in any way. PGS helps minimize the chances of using poor quality embryos which are responsible for lowering the patient’s chances of getting pregnant, increasing the chances of miscarriage, and generally cause various birth defects.
We are proud to offer our female patients access to the newest fertility technology available: NGS (Next-Generation Sequencing). NGS allows testing embryos which were obtained through IVF to a comprehensive analysis of their chromosomes. It is now on its way to completely replacing PGS as a more advanced procedure because it is more affordable and less prone to errors. Using NGS, fertility experts are able to gain insight into the defining characteristics of an embryo by analyzing its chromosomes on a more detailed and precise level than all other genetic tests can provide.
NGS is capable of detecting a lot more translocations than PGS, so its results are more detailed and reliable. It also requires less time for its completion, allowing for faster and more accurate results. Experts advise combining NGS with PGD to obtain the most comprehensive understanding of an embryo’s chromosomes and genetic potential. NGS analyzes the chromosomes on such a deep level that it is also capable of detecting different chromosomal traits in a single cell – a condition known as mosaicism.
Well, using NGS analysis, you can minimize the chances of a miscarriage, maximize the success rate of an IVF cycle, keep multiple pregnancies under control by transferring single embryos, maximize the overall chance of a successful pregnancy, and increase the chances of a live and healthy child being born. Women who are older than 35 are considered to be of advanced maternal age, and their embryos are more likely do display chromosomal abnormalities.
This is where NGS is particularly useful: it helps detect embryos that have a regular number of chromosomes (euploid), thus minimizing the chances of genetic abnormalities. Combining NGS with PGS allows doctors to obtain the clearest understanding of an embryo’s genetic potential based on multiple analysis tools and methods. This way, the probability of a seemingly healthy embryo turning out to be abnormal is minimized.
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