
HDPCR™ Non-Invasive Prenatal Testing Panel*
For research use only. Not for use in diagnostic procedures.

Rapid turnaround
Go from sample run to report in under 2 days

Cost effective
Implement on dPCR platforms without investing in complex and costly NGS workflows

Accessible
Upload assay data into ChromaCode Cloud for seamless adoption and interpretation of results
Trisomies Covered
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex Chromosome Abnormalities
Monosomy X (Turner syndrome), XO, XXX, XXY, XYY
Product benefits
Decrease time to identification with the utilization of dPCR and a standard workflow
Reduce costs while achieving the power of NGS on a dPCR platform
Gain accessibility with less complexity using HDPCR multiplexing

ChromaCode
reagents
Secure supply and common chemistry
dPCR instrument platforms
Wide range of platforms and simple data upload
Automated analysis with the ChromaCode Cloud
Advanced visualization and reporting with secure and scalable data management
Integration into lab reports
Generate comprehensive run summary and sample reports