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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

  • 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.

  • 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.

  • 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.

  • 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.

  • 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.

  • 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

  • Twin pregnancies


  • Non-invasive with no risk of miscarriage
  • Test from maternal blood sample as early as week 9 of pregnancy
  • Proven > 99% sensitivity for T21, 18 & 13, based on a study of nearly 147,000 pregnancies
  • Over 15,000,000 NIFTY® tests carried out to date by clinicians in more than 80 countries
  • Screening options for T21 (Down syndrome), 18 (Edwards syndrome) & 13 (Patau syndrome)
  • Results for 7-10 days
  • Singleton pregnancies


  • Non-invasive with no risk of miscarriage
  • Test from maternal blood sample as early as week 9 of pregnancy
  • Proven > 99% sensitivity for T21, 18 & 13, based on a study of nearly 147,000 pregnancies
  • Over 15,000,000 NIFTY® tests carried out to date by clinicians in more than 80 countries
  • Screening options for over 94 different genetic conditions + gender
  • Results for 7-10 days
  • Monogenetic abnormalities in singleton pregnancies


  • Non-invasive with no risk of miscarriage


  • Test from maternal blood sample as early as week 10 of pregnancy
  • 18 genes and over 2000 mutations are being examined
  • Screening options for: 27 monogenetic de novo genetic conditions
  • Proven > 99% sensitivity for all 27 monogenetic conditions
  • Results in 2 weeks

€1170

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Customer Feedback

What our customer say about us

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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!

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Marjana Zejnilovski

I have the best experience for both kids with nifty results on time and stem cell preservation service, the best laboratory.

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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.

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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!

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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.

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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.

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Tanja Kalovska

Highly professional.....I had very positive experience with Ginekalix

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Eli Fileva

Professional approach, affordable, efficient!

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Elena Trajanovska

Excellent, in every way 👏

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Jasmina Kostevska

The best

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Belma Pacariz

Professional, professional, the BEST! My warm recommendation for this genetic laboratory! Ginekalix Genetik Laboratory is a synonym for satisfaction!

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Admir Kjoroglu

Great experience....profesional all the way...just keep going....

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ana annna

Beautiful experience, professional at the highest level!

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Emma Nikolovska

Very professional. All the best⭐️

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Anastasija Ilievska

Top. Great experience. I recommend

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Angela Panchevska

Very pleased with everything!

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dejan jovanovski

Very nice

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Zo Kocev

Excellent

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Daniela Andreevska

Excellent experience so niv. Toplo gi preporacuvam. Fast, efficient, useful. Satisfied with every look from nivnata profesionalnost.

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Marija Kuzmanovic

Fast and flawless service. I highly recommend this laboratory for genetic testing.

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Marija Kolevska

Number 1 for prenatal and other genetic testing. Always the best and most professional

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a 007

Ginekaliks genetic laboratory number 1, profesionalnost i uslugi sekogas na nivo!

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Ginekalikslab

Laboratory of Medical Genetics and Genomics.

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+389 70 344 380 | +389 78 344 320