Preimplantation Genetic Diagnosis (PGD) has revolutionized the field of assisted reproductive technology (ART) by allowing embryologists to identify genetic abnormalities in embryos before implantation. This groundbreaking technique has empowered couples at risk of passing on genetic disorders to make informed decisions about their reproductive future. In recent years, significant advancements in PGD technologies and methodologies have further enhanced its accuracy, scope, and accessibility.
Next-generation sequencing (NGS) has emerged as a powerful tool in PGD, enabling comprehensive analysis of an embryo's entire genome. Unlike traditional methods like fluorescence in situ hybridization (FISH), which only examined a limited number of chromosomes, NGS can detect a wide range of genetic abnormalities, including aneuploidy (abnormal chromosome number), single-gene disorders, and structural rearrangements. This comprehensive analysis allows for more accurate and informed embryo selection, increasing the chances of a successful pregnancy and the birth of a healthy child.
Traditional PGD involves removing a few cells from the embryo for genetic testing, a process known as embryo biopsy. While generally safe, there is a small risk of damage to the embryo. Non-invasive PGD (niPGD) is a promising alternative that analyzes DNA fragments released by the embryo into the culture medium, eliminating the need for biopsy. This minimally invasive approach reduces the risk of embryo damage and may offer a more accurate assessment of the embryo's genetic makeup.
Artificial intelligence (AI) is making inroads into various aspects of healthcare, and PGD is no exception. AI algorithms can analyze vast amounts of data from embryo images and genetic tests to identify patterns and predict the likelihood of successful implantation. This data-driven approach can assist embryologists in making more informed decisions about embryo selection, potentially improving IVF success rates.
Traditionally, PGD focused on single-gene disorders and chromosomal abnormalities. However, with the advent of PGT-P, we can now assess embryos for their risk of developing complex, multifactorial conditions like heart disease, diabetes, and certain cancers. This opens up a new frontier in personalized medicine, allowing couples to make informed decisions based on their family history and genetic predispositions.
As a leading provider of precision instruments for assisted reproduction, Monash Biotech is proud to offer a range of micropipettes that are essential tools in PGD procedures. Our micropipettes are designed to facilitate precise and accurate embryo biopsy, ensuring the integrity of genetic material for analysis.
Our commitment to quality, reliability, and innovation makes Monash Biotech a trusted partner for fertility clinics and laboratories worldwide. We are dedicated to supporting advancements in PGD and other ART techniques to help more couples achieve their dream of having a healthy family.
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