Increase your chances of implantation

Preimplantation Genetic Testing (PGT)

PacGenomics is a global leader in reproductive genetic testing with products designed to help you build and grow a healthy family. We have designed our platform to provide the highest sensitivity in detection of genetic abnormalities allowing us to provide the most accurate and reliable results.

PGT is a genetic test used to analyze DNA from embryos produced through assisted reproductive techniques. PacGenomics’ PGT services include:

  • Preimplantation Genetic Testing for aneuploidies
  • Preimplantation Genetic Testing for chromosomal structural rearrangements
  • Preimplantation Genetic Testing to distinguish between normal and balanced carrier embryos in translocation cases
  • Preimplantation Genetic Testing for monogenic or single gene defects

The PGT Workflow



PGT starts with an embryo biopsy procedure in order to obtain sample cells for embryonic DNA analysis.


Samples are Sent
to PacGenomics

Your clinic then sends the samples to PacGenomics’ certified clinical genetics laboratory where PGT is performed.

PGT is

PacGenomics’ laboratory performs DNA sequencing and data analysis on the sample(s) received.


PGT Report

After testing data is analyzed, PacGenomics’ laboratory provides a PGT report for the referring REI physician.


Embryos chosen
for implantation

Based on the PGT report and a consultation with the physician, the patient can then make an informed selection as to which embryo(s) they’d like to have implanted.

Your Embryos Stay Safely in the IVF Clinic


Preimplantation Genetic Testing for Aneuploidies

Preimplantation Genetic Testing for Aneuploidy (PGT-A), formerly known as Preimplantation Genetic Screening (PGS), is a genetic test used to evaluate embryos produced through IVF for extra or missing chromosomes. Using genetic information gathered through PGT-A, your care team can select embryos that are best suited for transfer and increase your chances of successful pregnancy.

What are the benefits of PGT-A?

  • Higher pregnancy rates per transfer
  • Reduced risk of miscarriage
  • Reducing the number of IVF cycles needed to achieve pregnancy
  • Fewer implantation failures

Should I use PGT-A?

PGT-A is recommended for many people undergoing IVF treatment. All women have a chance of producing genetically abnormal embryos and this chance increases significantly as a woman ages. You may also consider PGT-A if you have experienced any of the following:

  • Repeated IVF treatment failure
  • Recurrent pregnancy loss
  • Previous child or pregnancy with a chromosomal abnormality


Preimplantation Genetic Testing for Chromosomal Structural Rearrangements

PGT-SR, or preimplantation genetic testing for chromosomal structural rearrangements is used to screen for embryos with detectable structural chromosomal abnormalities, including unbalanced translocations and inversions.

Testing is performed on embryos produced through assisted reproductive techniques (ART) and embryos with no detectable abnormality are chosen for transfer. By screening for abnormalities, you can increase your chances of achieving a successful pregnancy.



Preimplantation genetic testing to distinguish between normal and balanced carrier embryos in translocation cases

  • PGT-SR-Plus® can differentiate balanced translocation carrier embryos from normal embryos.
  • PGT-SR-Plus® does not require patient-specific probes to be built for testing.* Therefore, the turnaround time is not affected by the unique additional information offered with this platform.
  • PGT-SR-Plus® is seamlessly tailored to PacGenomics’ PGT-SR screening protocol, which has a successful record of identifying translocation carriers among patients who are not initially suspected to be at significant risk.

*Further, for most translocation screening cases at PacGenomics, an affected individual as a reference sample is not needed. Rare situations may arise (depending on the number of available embryos for testing) that prevent our team from conducting PGT-SR-Plus® testing on PGT-SR screened embryos.


Preimplantation Genetic Testing for Monogenic or Single Gene Defects

PacGenomics PGT-M is coming soon.

PGT-M is a genetic test designed for those who know they are at an increased risk of passing down a genetic disorder. PGT-M, or preimplantation genetic testing for monogenic/single gene defects was previously known as PGD, preimplantation genetic diagnosis. PGT-M is performed prior to pregnancy on embryos created through assisted reproductive techniques (ART). Only embryos without detectable monogenic disorders are then selected for transfer, greatly reducing the risk of having an affected child.