Proiecte Speciale
A pioneering family of tests providing greater confidence
About
Proiecte Speciale
Proiecte Speciale
PGT-Complete elevates aneuploidy testing standards.
PGT-A
Enhances IVF success by choosing the optimal embryo for transfer
Genetic PN check
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
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
Proiecte Speciale
Proiecte Speciale
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
Proiecte Speciale
Proiecte Speciale
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
Proiecte Speciale
Proiecte Speciale
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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
Proiecte Speciale
Proiecte Speciale
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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