The NIFTY® Test
The NIFTY™ Test – The World’s Leading Non-Invasive Prenatal Test (NIPT). Over 6 MILLION Samples Processed To Date.
During the last decade, developments in the science of genetics and enormous advances in genetic technologies have altered our capability to understand diseases, make diagnoses and provide effective treatments. Transforming the world of prenatal testing, the advent of new DNA-based non-invasive prenatal testing (NIPT) has introduced a highly accurate screening strategy for fetal anueploidy.
The NIFTY® test (Non-Invasive Fetal TrisomY test) was the first NIPT to enter clinical testing in 2010 and has been validated by a study on nearly 147,000 pregnancies. As of 2019, over 6,000,000 NIFTY® tests have been carried out worldwide.
NIFTY® offers screening for some of the most common trisomies present at birth, inluding trisomy 21 (Down Syndrome), trisomy 18 (Edwards Syndrome) and trisomy 13 (Patau Syndrome). NIFTY® also provides testing options for sex chromosomal aneuploidies, chromosomal deletions/duplications and gender.
Conditions Screened
| TRISOMIES | SEX CHROMOSOME ANEUPLOIDIES | DELETION/DUPLICATION SYNDROMES | GENDER IDENTIFICATION |
|---|---|---|---|
| Down Syndrome (T21) | Turner Syndrome (monosomy X) | Cri-du-chat Syndrome | Male/Female |
| Patau Syndrome (T13) | Klinefelter Syndrome (XXY) | 1p36 Deletion Syndrome | |
| T22 | Triple X Syndrome (XXX) | 2q33.1 Deletion Syndrome | |
| T16 | Jacob Syndrome (XYY) | Prader-Willi/Angelman Syndrome | |
| T9 | Jacobsen Syndrome | ||
| DiGeorge Syndrome II (10p14-p13) | |||
| 16p11.2-p12.2 Deletion/Duplication Syndrome | |||
| Van der Woude Syndrome |
A Comparison of Detection Rates
A Comparison of False Positive Rates (FPR)
NIFTY® Test Pro
NIFTY® Test Pro builds on the standard NIFTY® Test and provides expanded screening options covering all chromosomal numeric aneuploidies and 84 kinds of microdeletion/duplication syndromes.
Why Choose the NIFTY® Test Pro?
Conditions Screened
| TRISOMIES | SEX CHROMOSOME ANEUPLOIDIES | DELETION/DUPLICATION SYNDROMES | GENDER IDENTIFICATION |
|---|---|---|---|
| Down Syndrome (T21) | Turner Syndrome (monosomy X) | Wolf-Hirschhorn Syndrome | Male/Female |
| Edwards Syndrome (T18) | Klinefelter Syndrome (XXY) | DiGeorge Syndrome | |
| Patau Syndrome (T13) | Triple X Syndrome (XXX) | Miller-Dieker Syndrome | |
| T22 | Jacob Syndrome (XYY) | Prader-Willi/Angelman Syndrome (15q11.2) | |
| T16 | Williams Beuren Syndrome | ||
| T9 | Smith-Magenis Syndrome | ||
| Chromosome 1p36 Deletion Syndrome |