PGD-SEQ* kits offer over 500 gene panels to research embryo status of common and rare monogenic/single-gene diseases for IVF
With the power of Ion Torrent NGS technology, a single sample can be used for both PGT-A and PGT-M IVF investigations within a simplified and integrated workflow.
Each PGD-SEQ kit contains library preparation reagents necessary to enable preimplantation genetic testing for monogenetic/single-gene disorders (PGT-M). Benefits of using targeted NGS for PGT-M include:
- Verified for use with the Ion GeneStudio S5 System or Ion PGM System
- Complete kit reagents and targeted PGT-M library to analyze 15 samples
- Comprehensive familial carrier status using proprietary linkage analysis software
- Compatible with the Ion ReproSeq PGS Kit for combined PGT-M and PGT-A analysis from a single research sample
Featured PGD-SEQ solutions
SMN1 Panel and Reagent Kit for spinal muscular atrophy (SMA)
CFTR Panel and Reagent Kit for cystic fibrosis
COL1A1 Panel and Reagent Kit for osteogenesis imperfecta
FMR1 Panel and Reagent Kit for fragile X
HBA1/HBA2 Panel and Reagent Kit for alpha thalassemia
HBB Panel and Reagent Kit for beta thalassemia
Learn about PGT from key opinion leaders in the field
Simultaneously research PGT-A and PGT-M in the same NGS workflow from a single sample
Combine the PGD-SEQ kit with Ion ReproSeq PGS kit using the Ion GeneStudio S5 System for a simple, scalable and automated sample-to-answer workflow solution that includes PGT-M and PGT-A results from single research sample.
PGT-M ordering information
Consult an expert about how to bring simple, scalable and automated NGS to your lab, or inquire about the latest genes available for PGT-M.
* PGD-SEQ is a trademark of Bioarray, S.L.
For Research Use Only. Not for use in diagnostic procedures.