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Proiecte Speciale

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

  • Increase the chance of implantation and pregnancy

  • Reduce the risk of miscarriage

  • Reduce the time it takes for you to become pregnant

  • 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
  • 1,000 pregnancy outcomes used to generate baseline

  • Over 10,000 samples run to generate robust statistical analysis

User-Independent answers
  • Optimized and validated algorithms and automated analysis provide user-independent results

  • Automated analysis and interpretation

Proiecte Speciale

Proiecte Speciale

  • Suitable for people at high risk of passing on a specific single gene disorder

  • PGT-M testing examines both an individual’s mutation and the surrounding chromosome region

  • The testing process: case review, PGT-M test preparation, IVF & embryo biopsy, PGT-M, results & transfer

Proiecte Speciale

Proiecte Speciale

  • Tests embryos from IVF and only transfers normal ones.

  • Was formerly known as PGD, preimplantation genetic diagnosis

  • Suitable for individuals with chromosome rearrangements at risk of producing embryos with incorrect chromosome numbers or structures

  • Recommended when the partner carries a chromosomal rearrangement: inversion, reciprocal translocation, or robertsonian translocation

  • AI analysis, based on real outcomes, uses CNV & SNP to identify chromosomal rearrangements for robust, accurate results

  • Can identify specific abnormalities with 2-3 times greater resolution than most available tests