PGD-seq

PGD+PGS KITS

We present a genetic test specially designed to reduce the risk of having a child with an inherited condition.

WHAT IT IS?

PGD-Seq is a Kit and Software package to implement in your laboratory a PGD – PGD+PGS solution by NGS.

PGD-Seq represents a reproductive opportunity for couples who are exposed to an increased risk of having a child with a specific monogenic disorder e.g. cystic fibrosis, spinal muscular atrophy, beta thalassemia, polycytics kindey disease, marfan syndrome, fragile X syndrome, Huntington´s disease, etc.

PGD-SEQ WILL ALLOW YOU TO

Perform In-House and self-sufficient PGD analysis
Obtain quick results for fresh transfers
Simplify the PGD laboratory routine
Access more than 50 validated diseases
Order custom design of new monogenic diseases with no setup cost

HOW IT WORKS?

Nowadays, next generation sequencing (NGS) is the most effective technique available for the study of the genome. For this reason, it has become an important instrument for preimplantation genetic diagnosis.

It offers comprehensive information concerning aneuploidies, genetic mutations and unbalanced translocations in embryos.

PGD-Seq allows simultaneous detection of different point mutations and different SNPs surrounding them, thus eliminating the misdiagnosis risk by allele dropout (ADO). Ultimately it diagnoses each embryo as affected, carrier or unaffected.

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