"Empowering families with comprehensive PGT."

  Genoseq offers PGT-A/SR, advanced genetic testing to help select the healthy embryos for transfer
"Collaborating with physicians for informed embryo transfer decisions with PGT-A/SR"


"Comprehensive Genetic Screening for Improved Pregnancy Success"

Our thorough genetic screening improves pregnancy success rates by detecting chromosomal abnormalities and structural rearrangements in embryos

Personalized Care

"Personalized Care for Every Family's Unique Journey"

We provide personalized care tailored to the specific needs of each family, collaborating closely with physicians and patients.


"Understanding the Origin of Aneuploidy"

Through our advanced genetic screening, we strive to deepen our understanding of aneuploidy's origins, contributing to more accurate diagnostics.

PGT-A/SR: Peace

"PGT-A/SR: Peace of Mind for Patients and Clinical Teams"

PGT-A/SR offers peace of mind by identifying potential genetic issues before transfer, reducing the risk of implantation failure and miscarriage.

PGT-A/SR Detects

  • Whole chromosomal aneuploides
  • Partial segmental aneuploidies
  • Unbalanced translocations

Why perform PGT Aneuploidy (PGT-A/SR)

Aneuploidy in blastocyst embryos common
even in young women, with only a small percentage of
aneuploid embryos surviving to birth. The majority of then
results in failed implantation or miscarriage.

Process of PGT/SR

Process of PGT/SR

Test Results

Test Results Test Results Test Results

Test Results




Chances of implantation
and pregnancy


Very Low


Recommendations for transfer


Not Recommended


Contact Us

We'd love to work with you. Please fill out this form and our team will be in touch.


Who is PGT-M for?

PGT-M is indeed used to reduce the risk of passing on inherited genetic disorders to children, specifically for high-risk couples. It involves a clinical team providing personalized counseling and offering testing options to guide the process.

How it works

  • PGT-M (Preimplantation Genetic Testing for Monogenic disorders) identifies embryos with familial mutations causing inherited genetic disorders.
  • Couples can screen embryos for specific mutations to select those without the genetic mutation.
  • PGT-M reduces the risk of passing on the inherited disorder to future generations

Contact Us

We'd love to work with you. Please fill out this form and our team will be in touch.