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NIFTY® by Ginekaliks laboratory
NIFTY® is a non-invasive prenatal test that detects genetic disorders, such as Down's, Edwards' and Patau's syndrome, as early as the 10th week of pregnancy. NIFTY® has the widest panel of tests - it analyzes the entire genome of the baby - all 46 chromosomes.
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Medical genetics and genomics
Ginekaliks Genetic Laboratory, a laboratory for medical genetics and genomics where we offer a wide range of services: from preconception, pregnancy, newborn and throughout childhood and adulthood - which meet the needs of our patients and maintain the quality of health services at the highest level
Prenatal genetic / herediatary analyses
NIFTY® Pro, NIFTY® Twin, NIFTY® Mono, Vista™ CNVseq 100K, VISTRA CNVseq 1M, Conventional karyotype for couple, Vista™ MINI panel, Vista™ TARGETED panel, Vista™ MAX panel (1200+), Fragile X syndrome, Hemophilia A
Genetic risk factors
Microdeletions of Y chromosome, MTHFR / MTRR genes, Thrombophilia testing packages
Oncological inherited genetic panels
SENTIS BRCA, SENTIS, SENTIS FEMALE, SENTIS MALE
Newborn screening analyses
NOVA test, HEIDELBERG, Dietary screening test
Genetic diseases / panels
Clinical Whole Exome Sequencing (cWES), Clinical Whole Exome Sequencing + CNVseq, Clinical Whole Exome Sequencing - Trio, Clinical Whole Genome Sequencing (cWGS), Testing for 1 - 9 panel genes, Testing for 1 - 199 panel genes, 7. Testing for 200 + genes
Oncological genetic panels (blood / tissue)
SENTIS CANCER + DISCOVERY, SENTIS panel for lung cancer, SENTIS panel for colorectal cancer, SENTIS panel for gastric cancer, SENTIS panel for gastrointestinal stromal tumor
NIFTY® by Ginekaliks laboratory
Overview of NIFTY®
NIFTY® is a non-invasive prenatal screening test (or cell-free DNA screening) for pregnant women to assess the risk that the fetus will be born with certain chromosomal abnormalities. NIFTY® is available for singleton, twin and egg donor pregancies. Well-trusted in more than 11,520,000 pregnancies globally, NIFTY® can assess conditions that may affect your baby's health by doing a simple blood draw on you. NIFTY® screens for common chromosomal abnormalities, including trisomies, sex chromosome aneuploidies, and microdeletion/duplication syndromes, and can provide information about the sex of your babies.
NIFTY® by Ginekaliks laboratory
Why choose NIFTY®?
Reilable
More than 10 million pregnant women worldwide have taken the NIFTY® test so far, with the lowest false positive rate of 0.14%. Highest success rate of 99.902%
Safe & Fast
No risk for the baby and the laboring woman. Already from the 10th week of pregnancy, by analyzing a standard sample of 10 ml of maternal venous blood. Also suitable for twins, VTO and pregnancies with a donated egg. Result in 6-10 days.
Complete
NIFTY® and NIFTY® Pro tests analyze all 46 chromosomes of the baby. Broadest panel of tests: all trisomies (1-22), sex chromosome aneuploidies (X,Y), deletion/duplication syndromes (60 larger than 5Mb in the Plus package; 84 larger than 3Mb in the Pro package), incidental findings with clinical interpretation.
Precise
The rate of proven trisomy detection is greater than 99% and confirmed by the largest NIFTY® clinical trial in the world on almost 147,000 pregnancies.
NIFTY® by Ginekaliks laboratory
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 Ginekaliks laboratory
NIFTY® Workflow
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Order Your Prenatal Test Kit
Start by ordering our specialized prenatal test kit from our website. Designed for expectant mothers, this kit includes everything needed for a safe and easy blood sample collection
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Visit a Local Lab for Sample Collection
Take the test kit to any local laboratory. A trained healthcare professional will assist you in gently collecting a small blood sample. This process is quick and designed to ensure both your comfort and the reliability of the test
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Send Us the Blood Sample
Once your sample is collected, securely place it in the provided test tube and use the pre-addressed, postage-paid packaging to mail it back to our laboratory. We handle your sample with the utmost care and precision.
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Receive Comprehensive Prenatal Results
Our sophisticated lab will analyze your sample for a comprehensive prenatal diagnosis. We'll provide you with a detailed report that offers insights into your baby's health and development. You'll receive these results quickly and securely, enabling you to make informed decisions about your pregnancy
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
€740
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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
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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
€550
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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
€740
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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
-
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
€550
-
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
€740
-
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
Latest BGI technology
We are setting new standards of genetic screening!
Customer Feedback
What our customer say about us
Mjellma Doli
Marija Todorovska
Andrijana Todorovska
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
Andrijana Todorovska
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.
