Hours Hands-On Time
Hours on Amplification
Days faster than competing NIPTs*†
Lower failure rate‡
It's time to change the way you think about prenatal screening using NIPT. The VeriSeq NIPT Solution is a simple, noninvasive prenatal testing (NIPT) IVD solution for your lab that is now available in certain European Union countries. With only 2 hours of hands-on time and no PCR or amplification step, screening with NIPT has never been simpler.
The automated and validated workflow includes CE-marked sample prep and assay software. One lab technician can load a sequencer and get accurate results the following day. Are you ready to revolutionize your workflow?‡
*Assumes 1 workshift per day
† Data on file. Illumina, Inc. 2016.
‡ Data on file. Illumina, Inc. 2018.
The VeriSeq NIPT Solution is an in vitro diagnostic test intended for use as a sequencing-based screening test for the detection of fetal aneuploidies from maternal peripheral whole blood samples in pregnant women of at least 10 weeks gestation. VeriSeq NIPT provides information regarding aneuploidy status for chromosomes: 21, 18, 13, X, and Y. This product must not be used as the sole basis for diagnosis or other pregnancy management decisions.
Noninvasive prenatal testing (NIPT) based on cell-free DNA analysis from maternal blood is a screening test; it is not diagnostic. False positive and false negative results do occur. Test results must not be used as the sole basis for diagnosis. Further confirmatory testing is necessary prior to making any irreversible pregnancy decision. A negative result does not eliminate the possibility that the pregnancy has a chromosomal or sub chromosomal abnormality. This test does not screen for polyploidy (eg, triploidy), birth defects such as open neural tube defects, single gene disorders, or other conditions, such as autism. There is a small possibility that the test results might not reflect the chromosomal status of the fetus, but may instead reflect chromosomal changes in the placenta (confined placental mosaicism, CPM) or the mother that may or may not have clinical significance.