Secure and precise test for your baby's health, without any risk to your pregnancy.
Secure and precise test for your baby's health, without any risk to your pregnancy.
VeriSeq™ NIPT test – a worry-free start to parenthood.
Reliable non-invasive prenatal test that detects potential genetic anomalies as early as the 10th week of pregnancy, quickly, safely, and without pain.
What is the NIPT test and when can it be performed?
The NIPT test is a safe and reliable screening test for detecting genetic abnormalities in the fetus at the whole genome level from samples of peripheral whole blood of women who have been pregnant for at least 10 weeks.
When is it recommended?
The non-invasive prenatal test is recommended for all pregnant women who have a family history of chromosomal anomalies, those with a high risk based on the combined test, in cases where an ultrasound raises suspicion of anomalies, for women over the age of 35, and for those who have experienced a miscarriage in previous pregnancies.
How reliable is VeriSeq NIPT?
Compared to the traditional biochemical screening tests, NIPT offers a significantly higher level of sensitivity and specificity (>99.9%), as well as a much more comprehensive approach in the analysis of genetic anomalies.
Who can perform the VeriSeq NIPT test?
All pregnant women from the 10th week of pregnancy
Pregnant women over 35 years old
Pregnant women who have undergone IVF
Pregnant women with a family history of chromosomal disorders
Those at increased risk after the combined test
Pregnant women with twin pregnancies
Pregnant women who have experienced spontaneous miscarriages
What can VeriSeq NIPT detect?
Trisomy of chromosome 21 (Down syndrome)
Trisomy of chromosome 18 (Edwards sy.)
Trisomy of chromosome 13 (Patau syndrome)
Aneuploidies of sex chromosomes
Microdeletions and duplications larger than 7Mb
Aneuploidies of all autosomal chromosomes
Gender Determination
What are the benefits of the Veriseq NIPT test?
Test from full blood of a pregnant woman without risk to the mother or baby (Minimally invasive sampling)
First certified Illumina laboratory in the region (The test is fully conducted at ALEA Genetic Center)
99.9% accuracy for the detection of the most common chromosomal disorders
Rapid sample processing in BiH - results in a short time frame
Certified for diagnostic use (CE IVD)
Process for Patients
What does the testing process look like?
Blood draw at one of our laboratories
Sample processing at ALEA Genetic Center
Sample analysis using the most advanced technology
Collecting results in person or online
VeriSeq NIPT® Solution
The VeriSeq NIPT test enables reliable detection of chromosomal abnormalities from the 10th week of pregnancy – including Down, Edwards, and Patau syndromes. The analysis is conducted locally, without sending the sample outside of Bosnia and Herzegovina.
In collaboration with Nova Genetics
Twin Standard VeriSeq Package (Twin Pregnancy)
For pregnant women expecting twins who wish to have a basic NIPT screening.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Optional determination of baby gender
Twin Basic VeriSeq is a package designed for pregnant women carrying twins who desire a basic yet secure analysis of genetic risks. The test provides accurate results, making it a reliable choice. It is recommended as the first step in assessing the babies' health in the early stages of pregnancy.
Price:
1,050.00 BAM
Standard VeriSeq Package
For expectant mothers seeking a basic and reliable assessment of common chromosomal abnormalities.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Aneuploidies of sex chromosomes (e.g. Klinefelter, Turner, Triple X)
Optional determination of baby's sex
Silver VeriSeq is a basic package that provides reliable analysis of the most common chromosomal abnormalities in the fetus. The entire analysis process takes place locally at Alea Genetic Center, without sending samples abroad. This package is ideal for pregnant women who want timely information about basic genetic risks and security at the very beginning of pregnancy.
Price:
1,100.00 KM
Expert VeriSeq Package
For pregnant women seeking a comprehensive and detailed genetic analysis of the fetus.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex chromosome aneuploidies (e.g., Klinefelter, Turner, Triple X)
Microdeletions and microduplications ≥7 Mb
Aneuploidies of all autosomal chromosomes
Optional determination of the baby's sex
Platinum VeriSeq is the most comprehensive package when it comes to standard NIPT analyses, as it covers all chromosomes, including autosomal chromosomes. This thorough analysis provides the highest level of security and reduces the risk of missing genetic irregularities. It is the ideal option for expectant mothers who want a complete genetic analysis of the fetus without compromise.
Price:
1550.00 BAM
Twin Expert VeriSeq Package (Twin Pregnancy)
For pregnant women with twin pregnancies who seek additional security and a broader analysis.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Microdeletions (≥7 Mb) and duplications
Aneuploidies of autosomal chromosomes
Optional determination of baby gender
Twin Superior VeriSeq offers an expanded screening of genetic information in twin pregnancies. This package includes detection of microdeletions and autosomal aneuploidies, providing a more detailed analysis of the babies' health. It is recommended for pregnant women seeking a thoroughly comprehensive screening for twin pregnancies.
Price:
1550.00 BAM
Plus VeriSeq Package
For pregnant women seeking expanded genetic analysis covering microdeletions and duplications.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex chromosome aneuploidies (e.g., Klinefelter, Turner, Triple X)
Microdeletions and microduplications ≥7 Mb
Optional determination of the baby's sex
Gold VeriSeq offers an expanded analysis that, in addition to basic trisomies and aneuploidies, includes the detection of smaller structural changes in chromosomes (microdeletions and microduplications). This allows the identification of rare genetic syndromes not covered by basic tests. It is recommended for pregnant women who desire a more detailed insight into their child's genetic health and greater reassurance.
Price:
1,350.00 KM
Premium VeriSeq Package
For pregnant women seeking maximum safety and additional insight into the genetic health of the family.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex chromosome aneuploidies (e.g., Klinefelter, Turner, Triple X)
Microdeletions and microduplications ≥7 Mb
Aneuploidies of all autosomal chromosomes
Optional determination of baby's sex
MamaGEN test (screening the mother for monogenic disorders: cystic fibrosis, Wilson's disease, Gilbert's syndrome, spinal muscular atrophy, Duchenne muscular dystrophy).
If a mutation is found in the mother, testing the father for the same mutation is free of charge.
Brilliant VeriSeq is the most advanced package that offers not only a complete fetal analysis, but also a genetic screening for the mother. This package enables the detection of hereditary conditions that could affect the health of the baby or parents. It is recommended for pregnant women who seek the highest level of assurance and wish to obtain comprehensive information about their family's genetic health.
Price:
2,400.00 BAM
Twin Standard VeriSeq Package (Twin Pregnancy)
For pregnant women expecting twins who wish to have a basic NIPT screening.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Optional determination of baby gender
Twin Basic VeriSeq is a package designed for pregnant women carrying twins who desire a basic yet secure analysis of genetic risks. The test provides accurate results, making it a reliable choice. It is recommended as the first step in assessing the babies' health in the early stages of pregnancy.
Price:
1,050.00 BAM
Twin Expert VeriSeq Package (Twin Pregnancy)
For pregnant women with twin pregnancies who seek additional security and a broader analysis.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Microdeletions (≥7 Mb) and duplications
Aneuploidies of autosomal chromosomes
Optional determination of baby gender
Twin Superior VeriSeq offers an expanded screening of genetic information in twin pregnancies. This package includes detection of microdeletions and autosomal aneuploidies, providing a more detailed analysis of the babies' health. It is recommended for pregnant women seeking a thoroughly comprehensive screening for twin pregnancies.
Price:
1550.00 BAM
Standard VeriSeq Package
For expectant mothers seeking a basic and reliable assessment of common chromosomal abnormalities.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Aneuploidies of sex chromosomes (e.g. Klinefelter, Turner, Triple X)
Optional determination of baby's sex
Silver VeriSeq is a basic package that provides reliable analysis of the most common chromosomal abnormalities in the fetus. The entire analysis process takes place locally at Alea Genetic Center, without sending samples abroad. This package is ideal for pregnant women who want timely information about basic genetic risks and security at the very beginning of pregnancy.
Price:
1,100.00 KM
Plus VeriSeq Package
For pregnant women seeking expanded genetic analysis covering microdeletions and duplications.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex chromosome aneuploidies (e.g., Klinefelter, Turner, Triple X)
Microdeletions and microduplications ≥7 Mb
Optional determination of the baby's sex
Gold VeriSeq offers an expanded analysis that, in addition to basic trisomies and aneuploidies, includes the detection of smaller structural changes in chromosomes (microdeletions and microduplications). This allows the identification of rare genetic syndromes not covered by basic tests. It is recommended for pregnant women who desire a more detailed insight into their child's genetic health and greater reassurance.
Price:
1,350.00 KM
Expert VeriSeq Package
For pregnant women seeking a comprehensive and detailed genetic analysis of the fetus.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex chromosome aneuploidies (e.g., Klinefelter, Turner, Triple X)
Microdeletions and microduplications ≥7 Mb
Aneuploidies of all autosomal chromosomes
Optional determination of the baby's sex
Platinum VeriSeq is the most comprehensive package when it comes to standard NIPT analyses, as it covers all chromosomes, including autosomal chromosomes. This thorough analysis provides the highest level of security and reduces the risk of missing genetic irregularities. It is the ideal option for expectant mothers who want a complete genetic analysis of the fetus without compromise.
Price:
1550.00 BAM
Premium VeriSeq Package
For pregnant women seeking maximum safety and additional insight into the genetic health of the family.
What is included:
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex chromosome aneuploidies (e.g., Klinefelter, Turner, Triple X)
Microdeletions and microduplications ≥7 Mb
Aneuploidies of all autosomal chromosomes
Optional determination of baby's sex
MamaGEN test (screening the mother for monogenic disorders: cystic fibrosis, Wilson's disease, Gilbert's syndrome, spinal muscular atrophy, Duchenne muscular dystrophy).
If a mutation is found in the mother, testing the father for the same mutation is free of charge.
Brilliant VeriSeq is the most advanced package that offers not only a complete fetal analysis, but also a genetic screening for the mother. This package enables the detection of hereditary conditions that could affect the health of the baby or parents. It is recommended for pregnant women who seek the highest level of assurance and wish to obtain comprehensive information about their family's genetic health.
Price:
2,400.00 BAM
Note for Donor or IVF Pregnancies
Each of the mentioned packages (Twin Standard, Twin Expert, Standard, Plus, Expert, Premium) can be customized for pregnant women who have undergone the in vitro fertilization (IVF) process or used donor eggs, without any additional cost apart from the selected package.
Our Team
Geneticists dedicated to your health
Our multidisciplinary team consists of experienced experts from various fields of genetics.
Locations
Visit us at the following location
Alea Genetic Center (AGC)
Olovska 67, 71000 Sarajevo
+387 33 867 589
info@agc.ba
Monday – Friday: 09:00 – 17:00
Alea Genetic Center (AGC)
Olovska 67, 71000 Sarajevo
+387 33 867 589
info@agc.ba
Monday – Friday: 09:00 – 17:00
Second medical opinion
Request a second opinion
For any additional questions, you can contact us. All you need to do is fill out and submit the form.
Frequently Asked Questions
Frequently Asked Questions
Find answers to frequently asked questions about our services, appointment scheduling, preparation for examinations, and other important information.
How can I schedule an appointment?
Is a referral required for the examination?
What payment methods are available?
Do you provide emergency medical services?
How long does a systematic exam take?
Frequently Asked Questions
Frequently Asked Questions
Find answers to frequently asked questions about our services, appointment scheduling, preparation for examinations, and other important information.
How can I schedule an appointment?
Is a referral required for the examination?
What payment methods are available?
Do you provide emergency medical services?
How long does a systematic exam take?
Frequently Asked Questions
Frequently Asked Questions
Find answers to frequently asked questions about our services, appointment scheduling, preparation for examinations, and other important information.
How can I schedule an appointment?
Is a referral required for the examination?
What payment methods are available?
Do you provide emergency medical services?
How long does a systematic exam take?