
Genetic Testing
A pioneering family of tests providing greater confidence
About
Test packages
PGT-CompleteSM – 4 in 1 genetic test
Test packages
PGT-Complete elevates aneuploidy testing standards.
PGT-A
Enhances IVF success by choosing the optimal embryo for transfer
Genetic PN check
Provide genetic information for correct embryo fertilisation
Gives the capability to identify and rescue true 2PN embryos from morphologically identified 0, 1, and 3PN embryos
Parental QC
Reassure patients that the intended egg and sperm were used
Confirms a match between embryo biopsy and parental samples
Alleviates anxiety for both clinicians and patients
Origin of Aneuploidy
Identifies abnormality origin, guiding future decisions
Directly assesses gametic contribution to embryo aneuploidy
- >10% of whole chromosome aneuploidy is of paternal origin
- 70% of segmental aneuploidy is of paternal origin
PGT-A
Preimplantation Genetic Testing for Aneuploidies (PGT-A)
Benefits
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Increase the chance of implantation and pregnancy
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Reduce the risk of miscarriage
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Reduce the time it takes for you to become pregnant
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Reduce the potential emotional, physical and financial impact of multiple IVF cycles

PGTaiSM
The most sophisticated PGT-A analysis algorithm
First PGT-A analysis software to deliver true statistical analysis of data
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1,000 pregnancy outcomes used to generate baseline
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Over 10,000 samples run to generate robust statistical analysis
User-Independent answers
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Optimized and validated algorithms and automated analysis provide user-independent results
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Automated analysis and interpretation
PGT-M
Designed to reduce the risk of inherited disorders in children
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Suitable for people at high risk of passing on a specific single gene disorder
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PGT-M testing examines both an individual’s mutation and the surrounding chromosome region
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The testing process: case review, PGT-M test preparation, IVF & embryo biopsy, PGT-M, results & transfer
PGT-SR
Detecting chromosomal rearrangement
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Tests embryos from IVF and only transfers normal ones.
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Was formerly known as PGD, preimplantation genetic diagnosis
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Suitable for individuals with chromosome rearrangements at risk of producing embryos with incorrect chromosome numbers or structures
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Recommended when the partner carries a chromosomal rearrangement: inversion, reciprocal translocation, or robertsonian translocation
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AI analysis, based on real outcomes, uses CNV & SNP to identify chromosomal rearrangements for robust, accurate results
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Can identify specific abnormalities with 2-3 times greater resolution than most available tests