Benefits of NIPT Limitations of NIPT
Non-invasive with no risk of miscarriage. NIPT is a screening test, not a diagnostic test and must be followed up with an invasive test if a definitive diagnosis is needed.
High detection rates for chromosomes tested. In rare instances, results may represent a maternal or placental condition, rather than a fetal condition.
High sensitivity and specificity compared to traditional serum screening.  

TriScreen NIPT uses whole genome sequencing with next generation sequencing (NGS) technology to analyse cell-free DNA (cfDNA) fragments across the whole genome, which has proven advantages over other NIPT methodologies such as targeted sequencing and array-based methods.

Test failure rates are substantially lower with whole genome sequencing versus other methodologies4, 7-9.

With its high levels of sensitivity and accuracy, NGS produces the data quality needed for reliable analysis of the trace amounts of cfDNA found circulating within blood plasma.

Benefits of NIPT Limitations of NIPT
Non-invasive with no risk of miscarriage NIPT is a screening test, not a diagnostic test and must be followed up with an invasive test if a definitive diagnosis is needed.
High detection rates for chromosomes tested In rare instances, results may represent a maternal or placental condition, rather than a fetal condition.
High sensitivity and specificity compared to traditional serum screening.  
Performance Metrics
Chromosome N Sensitivity 95% CI Specificity 95% CI
Trisomy 21 2236 99.9% (130/130) 97.1 - 100.0 99.90% (1982/1984) 99.63 - 99.97
Trisomy 18 2236 99.9% (41/41) 97.4 - 100.0 99.9% (1995/1997) 99.64 - 99.97
Trisomy 13 2235 99.9% (14/16) 87.1 - 100.0 99.9% (2000/2002) 99.64 - 99.97
RAA** 2300 96.4% (27/28) 82.3 - 99.4 99.8% (2001/2005) 99.49 - 99.92
CNV > 7Mb 2300 74.1% (20/27) 55.3 - 86.8 99.8% (200/2004) 99.49 - 99.92
Any anomaly*** 2300 95.5% (318/333) 92.7 - 973 99.35% (1954/1967) 98.87 - 99.61
*Data from VeriSeq NIPT Solutions v2 package insert
**RAA excludes chromosomes 31, 18, 13
***Includes sex chromosome anomalies from genomewide screen
Key:
N: Sample Size
RAA: Rare Autosomal Aneuploidy
CI: Confidence interval
CNV: Copy number variation

Powered by Illumina, global leader in next generation sequencing.

illumina

Next Biosciences has been offering the Illumina NIPT test in South Africa since 2016.

Dedicated

In-house processing ensuring a quicker turnaround time.

In House

VeriSeqTM NIPT Solution V2, providing the most comprehensive view of genomewide fetal chromosomal anomalies.

VeriSeq

1.2% Failure rate (resulting in less re-draws than other tests).

LowFailure

A high accuracy with low fetal fraction - No fetal fraction cut-off (relies on a dynamic threshold (iFact), which reduces NIPT failures).

iFact

Access to specialist team of Genetic Scientists, a Medical Doctor, Pathologist and Genetic Counsellor.

GeneticScientest

One free genetic counselling session for all high risk results, providing your patients with the support they need.

Free Genetic Counselling

Dedicated client service team to support both you and your patients.

Dedicated

TriScreen
Non-Invasive Prenatal Testing (NIPT)

Screening of cell-free fetal DNA for common chromosomal conditions,
from 10 weeks gestational age.

Chromosome 21 (T21)

R

4 100

Chromosome 21, 18, 13, X&Y

R

5 950

All Chromosomes

R

6 500

Chromosome 21, 18, 13, X&Y & Microdeletions*

R

8 500

All Chromosome & Microdeletions*

R

10 500


Microdeletions includes the following syndromes: 22q11 deletion (Di George), 15q11 deletion (Angelman/Prader-Willi), 1p36 deletion; 4p- (Wolf-Hirschhorn), and 5p- (Cri-du-chat)
 

Chromosome 21, 18, 13 X&Y, and Fetal RhD

R

6 500

Chromosome 21, 18, 13 X&Y, and 22q11 deletion (Di George)

R

6 500

*Please note that all prices include VAT and are subject to change.

  • TriScreen NIPT (Standard Panel)

    T21 (Down syndrome), T18 (Edward syndrome), T13 (Patau syndrome)

  • TriScreen NIPT + (All Chromosomes)

    Provides chromosomal status for all chromosomes and segmental deletions and duplications >7Mb.

  • Optionally reported

    Information on the status of fetal sex chromosomes and certain sex chromosome aneuploidies.

  • Addition of Microdeletions

    Chromosome 21, 18, 13 X&Y with 22q deletion only (Di George), 15q11 deletion (Angelman/Prader-Willi), 1p36 deletion, 4p (Wolf-Hirschhorn) 5p (Cri-du-chat)

    *Additional blood draw arrangements and logistics are required.
    *Please note that Microdeletion samples are currently sent to the United States.

  • Rhesus testing

    Chromosome 21, 18, 13 X&Y with the addition of fetal RhD status assessment

    *Additional blood draw arrangements and logistics are required.

TriScreen NIPT can be performed on:

  • Singleton pregnancies
  • Twin pregnancies
  • Donor pregnancies
  • IVF pregnancies (from 8 weeks post-implantation)
  • Surrogate pregnancies

NIPT analyses cell-free DNA from a maternal blood sample (mixture of placental and maternal DNA) to screen for common chromosomal conditions including trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome).

Genomewide NIPT screening allows not only for the detection of common chromosomal aneuploidies but provides a comprehensive view of all 23 chromosome pairs. It enables the identification of rare autosomal aneuploidies (RAAs), sex chromosome aneuploidies (SCAs) as well as partial deletions and duplications (also referred to as copy number variations CNVs) that are ≥7 Mb in size.

These additional chromosomal abnormalities have been associated with clinically relevant outcomes such as developmental delays, intellectual disabilities, structural anomalies and adverse pregnancy outcomes.

Having insight into these chromosomal abnormalities earlier may assist you and your patient in the management of the pregnancy.

CfDNA Tube

The American Congress of Obstetricians and Gynaecologists (ACOG) and International Society of Prenatal Diagnosis (ISPD), along with other professional societies, have stated that NIPT is an available screening option for all pregnant women1,8.

NIPT vs. traditional serum screening methods:

  • Offers the highest reported detection rate for Down syndrome2
  • Offers the lowest reported false positive rate for Down syndrome3
  • Offers the broadest screening window (performed as early as 10 weeks gestation until term)2

Next Biosciences is proud to be a valued member of The Global NIPT consortium alongside other Illumina-powered laboratories.

NIPT Methodology updated version

Disclaimer:
Non-Invasive Prenatal Testing (NIPT) based on cell-free DNA analysis from maternal blood is a screening test; it is not diagnostic. Test results must not be used as the sole basis for diagnosis. Further confirmatory testing is necessary prior to making any irreversible pregnancy decision.

  1. Benn P, Borrell A, Chiu R, et al. Position statement from the Chromosome Abnormality Screening Committee on behalf of the board of the International Society for Prenatal Diagnosis. Prenat Diagn. 2015;35(8):725-734.
  2. American College of Obstetricians and Gynecologists: Screening for fetal aneuploidy. Obstet Gynecol. 2016;127(5):e123-137.
  3. Bianchi DW, Parker RL, Wentworth J, et al. DNA sequencing versus standard prenatal aneuploidy screening. N Engl J Med. 2014;370(9):799-808.
  4. Data calculation on file. Illumina, Inc. 2017.
  5. VeriSeq NIPT Solution Package Insert.
  6. Data calculation on file. Illumina, Inc. 2018.
  7. VeriSeq NIPT Solution v2 Package Insert.
  8. Committee Opinion No. 640: Cell-free DNA Screening for Fetal Aneuploidy. Obstet Gynecol. 2015;126(3):e31-37.

All pregnant women can be offered the option of NIPT.

Patients can be at high risk for aneuploidy due to:

  • Maternal age-related risks
  • Positive results on maternal-serum screening
  • Abnormal ultrasound finding(s)
  • History suggestive of increased risk for T21, T18, T13 or sex chromosome aneuploidy
  • Parental translocation involving one of the tested chromosomes (depending on size)

Indications for all chromosome test:

  • History of a pregnancy with chromosomal abnormality
  • Abnormal ultrasound findings and patient wants to avoid invasive test
  • One of the parents are known to be a carrier of a balanced translocation (depending on size)
  • Patients who want more detailed information and have had a genetic counselling appointment to understand the limitations of the test, and the possibility of false positives and negatives.

Anyone considering genomewide testing is strongly advised to have an appointment with a genetic counsellor / detailed discussion with their obstetrician (regardless of the indication).

 

PRICING
SINGLETON PREGNANCY
Chromosome 21 R 3900

Chromosome 21, 18, 13, X&Y
-Includes sex chromosome anomalies

 R 5500
All Chromosomes R 6500

Chromosome 21, 18, 13, X&Y & Microdeletions*
-Includes sex chromosome anomalies

 R 8500

All Chromosome & Microdeletions*
*Microdeletions 22q11 deletion (DiGoerge), 15q11 deletion (Angelman/Prader-Willi), 1p36 deletion, 4p- (Wolf-Hirschhorn), 5p- (Cri-di-chat)

 R 13500
TWIN PREGNANCY

Chromosome 21, 18, 13
(Includes presence/absence of Y chromosome-no anomalies tested)

 R 5500