NIPT™
About NIPT™
It is a safe, highly-accurate examination service possible after 10 weeks of pregnancy through non-invasive, pre-birth examination to detect fetal chromosome abnormalities (aneuploidy) through NGS (Next-Generation Sequencing) by extracting fetal DNA from pregnant women’s blood.
Strengths
Non-invasive examination
It is examined with pregnant women’s blood, eliminating the risk of fetal infection, early contraction or miscarriage
High sensitivity and accuracy
It displays extremely high accuracy, sensitivity and specificity.
Early detection of chromosomal abnormality
It is possible to quickly and accurately detect abnormal number of chromosomes after 10 weeks of pregnancy.
Quick Examination Results
Using NGS, it is possible to find out the examination result within 7 days from the day of blood extraction.
Isolations
According to the method of blood separation and isolation of targeted particles, different cartridges are provided.
Examination Content
Autosomal abnormality
Abnormality in specific number of autosomes
Down Syndrome, Edward Syndrome, Patau Syndrome.
Sex chromosome abnormality
Abnormality in the number of sex chromosomes
Abnormality in the numbers of chromosomes excluding those of Turner Syndrome, Klinefelter Syndrome, Triple X Syndrome and Jacobs Syndrome.
Examination Procedure
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