Get NIFTY® Pro
Free of charge
Valid until 30.11.2024
NIFTY® Pro
by Ginekalikslab
NIFTY® Pro is the ultimate non-invasive prenatal test that offers expectant parents comprehensive insight into their baby's health. Using advanced fetal DNA genetic sequencing technology, NIFTY® Pro screens for 94 genetic conditions, including Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome) and sex chromosome aneuploidies, with extended screening for rare autosomal aneuploidies and microdeletion and microduplication syndromes.
NIFTY® by Ginekalikslab
Overview of NIFTY® Pro
The NIFTY® Pro test is an advanced non-invasive prenatal test (NIPT) developed by BGI Genomics. It is part of the broader NIFTY® (Non-Invasive Fetal TrisomY) series of tests, which are widely used to screen for chromosomal abnormalities during pregnancy. The NIFTY® Pro test is particularly known for its comprehensive screening capabilities, offering insights into a range of chromosomal conditions with a high degree of accuracy. NIFTY® Pro offers a more extensive screening panel compared to the standard NIFTY® test. It covers 94 chromosomal conditions, including rare trisomies, fetal sex aneuploidies and microdeletions. The test uses advanced sequencing technology and bioinformatics analysis to provide highly accurate results, with sensitivity and specificity rates typically above 99% for common trisomies. It is a valuable tool in prenatal screening, offering a comprehensive analysis of the fetus's chromosomal health. Its advanced technology and wide coverage make it an excellent option for expectant parents looking for detailed information about their pregnancy.
NIFTY® by Ginekalikslab
Why choose NIFTY® Pro?
Safe: Non-invasive with no risk of miscarriage
Simple: Test from a small maternal blood sample (~5ml)
Early: The test could be done as early as 10 gestational weeks of pregnancy
Quick: Turnaround within 7 days
Accurate: Proven sensitivity with more then 99%, based on a study of nearly 147,000 pregnancies
Trusted: Over 11,000,000 NIFTY® tests carried out to date by clinicians from more than 80 countries
NIFTY® by Ginekalikslab
How NIFTY® test works?
During pregnancy, fetal DNA enters into maternal bloodstream. Next-generation technology makes it possible to analyze free fetal DNA segments that are present in maternal blood in order to identify chromosomal abnormalities. NIFTY® test requires only 10 ml maternal blood sample and blood collection can be performed during the 10th pregnancy week.
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NIFTY® by Ginekalikslab
NIFTY® Pro Workflow
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Pre-Test Counseling: Call our laboratory to consult with our geneticists free of charge and find all the answers to your questions so you can choose the best option for your baby.
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Order your prenatal test kit: Start by ordering our specialized prenatal test kit from our website. This is supported by a global leader in the logistics industry. Designed for expectant mothers, this kit includes everything needed to safely and easily collect a blood sample.
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Visit a local laboratory for sample collection: Take the test kit to any local laboratory. A trained healthcare professional will help you gently collect a small 10ml blood sample. This process is non-invasive and 100% safe for yourself and your baby. It is quick and designed to ensure both your test convenience and confidentiality.
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Send us a blood sample: Once your blood sample is collected, place it securely in the box provided and use the pre-addressed, postage-paid packaging to send it back to our laboratory.
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Laboratory Analysis: Our sophisticated laboratory will analyze your sample for a comprehensive prenatal diagnosis. The fetal DNA is being isolated from the mother's blood and is being tested with the advanced NGS technology (CNV > 3 Mb) across the whole genome with a 99% accuracy.
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Reporting and interpretation: We will inform you on the phone and provide you via email with a detailed report that offers information for more than 94 genetic abnormalities (Trisomy 21, 18, 13, 16, 22, 9, sex chromosomal aneuploidies: XO, XXX, XXY, XYY, 84 deletions and duplications + incidental findings) related to your baby's health and development. You will receive these results in 7 – 10 days quickly and safely, while having the chance to discuss the results with our specialized team and geneticists. They will help you understand your results and make sure you receive all the information, any time, 24/7 at your disposal.
Why NIFTY®?
Why you should choose NIFTY®
| NIFTY® (Non-Invasive Fetal Trisomy) | First Trimester Screening | Quad Screen | |
|---|---|---|---|
| Timing of Test | After 9 weeks of pregnancy | 11-14 weeks of pregnancy | 15-20 weeks of pregnancy |
| Detection Rate for Trisomy 21 | ~99% | ~85-90% | ~80-85% |
| Detection Rate for Trisomy 18 | ~97% | ~80% | ~70-80% |
| Detection Rate for Trisomy 13 | ~95% | ~70% | ~60-70% |
| False Positive Rate | ~0.1% | ~5% | ~5% |
| Invasive Testing Required | No | No | No |
| Risk of Miscarriage | None | None | None |
| Accuracy | Very High (based on analysis of fetal DNA) | Moderate (based on a combination of blood markers and ultrasound) | Moderate (based on multiple serum markers) |
| Follow-Up Testing | If high risk is indicated, diagnostic tests (e.g., amniocentesis or CVS) | If high risk is indicated, diagnostic tests | If high risk is indicated, diagnostic tests |
| Test Procedure | Simple blood draw from mother | Blood test and ultrasound combined | Blood test from mother |
| Turnaround Time for Results | Typically 1-2 weeks | Typically 1-2 weeks | Typically 1-2 weeks |
| Impact on Pregnancy Management | Helps inform about risk, can lead to more targeted diagnostic testing | Helps assess risk but might lead to further testing | Helps assess risk but might lead to further testing |
Choose from our affordable 3 packages!
Compare packages to find the best solution
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Twin pregnancies
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Non-invasive with no risk of miscarriage
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Test from maternal blood sample as early as week 9 of pregnancy
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Proven > 99% sensitivity for T21, 18 & 13, based on a study of nearly 147,000 pregnancies
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Over 15,000,000 NIFTY® tests carried out to date by clinicians in more than 80 countries
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Screening options for T21 (Down syndrome), 18 (Edwards syndrome) & 13 (Patau syndrome)
- Results for 7-10 days
€550
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Singleton pregnancies
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Non-invasive with no risk of miscarriage
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Test from maternal blood sample as early as week 9 of pregnancy
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Proven > 99% sensitivity for T21, 18 & 13, based on a study of nearly 147,000 pregnancies
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Over 15,000,000 NIFTY® tests carried out to date by clinicians in more than 80 countries
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Screening options for over 94 different genetic conditions + gender
- Results for 7-10 days
€670
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Monogenetic abnormalities in singleton pregnancies
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Non-invasive with no risk of miscarriage
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Test from maternal blood sample as early as week 10 of pregnancy
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18 genes and over 2000 mutations are being examined
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Screening options for: 27 monogenetic de novo genetic conditions
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Proven > 99% sensitivity for all 27 monogenetic conditions
- Results in 2 weeks
€1170
Latest BGI technology
We are setting new standards of genetic screening!
Customer Feedback
What our customer say about us
Jovana Marojevikj
5/5 score for the services they offer. The staff is very friendly and helpful, they will guide you through every step and will explain everything for the analysis you are doing. I had an amazing experience and I highly recommend choosing Ginekaliks!
Marjana Zejnilovski
I have the best experience for both kids with nifty results on time and stem cell preservation service, the best laboratory.
Elena Spasovska
Great experience with GINEKALIKS LABORATORIJA. Their customers for Nifty and mother cells. Satisfied in every way, from their patience to their professionalism. I highly recommend them.
Marija Stojanovska Bujaroska
Extremely satisfied with the service and the kind personnel, genetic analysis is a delicate subject to discuss about. Would definitely recommend should you need any type of analysis this laboratory offers!
Cvetanka Jovanovska
Positive experience, available at any time to answer any question, clear and concise in what they offer, ready to meet any request.
Positive and cheerful medical representatives.
Huge recommendation.
Eldina Pachariz
I am extremely satisfied with the team and expertise in the interpretation of my result. Strongly suggest to others with all genetic problems.
Tanja Kalovska
Highly professional.....I had very positive experience with Ginekalix
Eli Fileva
Professional approach, affordable, efficient!
Elena Trajanovska
Excellent, in every way 👏
Jasmina Kostevska
The best
Belma Pacariz
Professional, professional, the BEST! My warm recommendation for this genetic laboratory! Ginekalix Genetik Laboratory is a synonym for satisfaction!
Admir Kjoroglu
Great experience....profesional all the way...just keep going....
ana annna
Beautiful experience, professional at the highest level!
Emma Nikolovska
Very professional. All the best⭐️
Anastasija Ilievska
Top. Great experience. I recommend
Angela Panchevska
Very pleased with everything!
dejan jovanovski
Very nice
Zo Kocev
Excellent
Daniela Andreevska
Excellent experience so niv. Toplo gi preporacuvam. Fast, efficient, useful. Satisfied with every look from nivnata profesionalnost.
Marija Kuzmanovic
Fast and flawless service. I highly recommend this laboratory for genetic testing.
Marija Kolevska
Number 1 for prenatal and other genetic testing. Always the best and most professional
a 007
Ginekaliks genetic laboratory number 1, profesionalnost i uslugi sekogas na nivo!
Katerina Davidovska
Andrea Risteska
Elena Panic
Katerina Janevska
Mila Najmila
Ramazan Ismailovski
Dragana Dojchinovska
Monika Panevska
Natalija Stojmanovska
Marija Mitevska
Marija Velkova
Meri Trpeska
tija avramovic
Elena Panic
Verica Mirchev
Veronika Ivanovska
Ivana Rizovski
Martina Zdravkovska Vandev
Maja Chochevska
Mjellma Doli
Marija Todorovska
