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Veriref® is a high-precision non-invasive prenatal test (NIPT) that detects the risk of aneuploidies on chromosomes 13, 18, 21, X and Y of the fetus, studying the fetal DNA in maternal blood. VeriRef® also reports fetal sex.
For those cases in which more information is required, we have developed VeriRef Premium®, which detects aneuplodia and CNVS in all chromosomes.
Suitable for any BMI, ethnic group, invitro fertilization and egg donation.
All equipment: platform, software and consumables endowed with the CE-IVD marking.
It quantifies in a detailed and very sensitive way the fetal fraction of each sample.
In high-risk results, an immediate warning is given and FREE CONFIRMATION BY QF-PCR or CGH Array is offered from an amniotic fluid sample.
Has the lowest rate of failure to obtain results: <0.1%
Currently operational integration of results in any SIL of the Laboratory.
Test with the largest number of publications that support it (Veri® and VeriSeq® from ILLUMINA).
Technology: MPS-Massive Parallel Sequencing m (whole genome sequencing). It will allow the incorporation of new developments in the future.
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