*Schedule shown is an estimate. Timelines may vary from lab to lab
The VeriSeq NIPT Solution v2 provides everything needed for NIPT using NGS, including reagents for DNA extraction, library prep, and sequencing; instrumentation to automate library prep and sequencing with workflow manager software; an onsite server for secure data storage and analysis; and data analysis software capable of generating a report that provides qualitative results.
Results that you and your clinicians can trust.
a. Basic screen performance is reported for T21, T18, and T13 and excludes 16 samples with known mosaics and 49 samples affected with anomalies for the genome-wide screen only; genome-wide screen performance is reported for RAAs and CNVs.1
b. Seven twin pregnancies reported correctly as T21 are not shown in the table.1
c. RAA excludes chromosomes 21, 18, and 13.1
Interested in bringing the VeriSeq NIPT Solution v2 into your lab? Contact us today: