NIFTY Non-Invasive Prenatal NIPT Test

NIFTY Non-Invasive Prenatal NIPT Test

Disease: Genetics

Method: NGS DNA Sequencing

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Sample Types
  • Blood
  • Results in : 7 Days
  • Test Cost: 10,000.00/- Rs

NIFTY Non-Invasive Prenatal NIPT Test Cost 10000 Rs

Test type Gynecologist
Pre-test Information
Report Delivery 7 Days
Price ₹ 10000
Method NGS DNA Sequencing

NIFTY Non-Invasive Prenatal NIPT Test Details

Short Description

NIPT Test screens for trisomy 21 (Down Syndrome), 18 (Edward Syndrome), and 13 (Patau Syndrome) as early as 10 weeks of Pregnancy. This test is also known as NIFTY Test or Non Invasive Prenatal Test or Maternal Blood for Fetal DNA Test or NIPS Test

Test Specifications

  • Speciality: Gynecologist

  • Components:


  • Shipping Stability: Room 48Hrs

PreTest Information

Detail Description

NIFTY Non-Invasive Prenatal NIPT Test

DNA Labs India NIPT or Non-Invasive Prenatal test is performed, analyzed and supported by DNA Labs India's team of highly experienced laboratory scientists and genetic clinicians at an affordable. DNA Labs India is ranked as India's Most Trusted NIPT Testing facility by doctors and hospitals across India. DNA Labs India is an expert in genetic testing and a global leader in the diagnosis of rare genetic diseases. We conform to the highest standards for diagnostic testing and reporting.

NIPT Test screens for the three most common trisomy conditions present at birth which are:

  • Down Syndrome
  • Edwards Syndrome
  • Patau Syndrome.

Independent validation studies, including the world's largest study on the use of NIPT in clinical practice in nearly 147,000 women, have shown NIPT has an accuracy rate of over 99.99% for detection of these above conditions. THE TEST CAN ALSO DETECT additional chromosomal abnormalities

  • Turner syndrome (Monosomy X)
  • Klinefelter syndrome (XXY)
  • Jacobs syndrome (XYY)
  • Triple X syndrome (XXX)

How does the NIPT work?

Small amounts of a baby's DNA pass into the bloodstream of the mother during pregnancy. Cell-free DNA fragments (cfDNA) are short fragments of DNA, which can be found circulating in the mother's blood. 

New technology allows us to analyze this DNA directly from the mother's blood and screen for chromosomal abnormalities. cfDNA is then analyzed with our proprietary genetic sequencing technology and bioinformatics pipelines to screen for any chromosomal abnormality in the fetus. If any abnormality is present, small excesses or deficits in counts of the affected chromosome can be detected.

Until recently, it has only been possible to screen for abnormalities with highly invasive procedures such as chorionic villus sampling (CVS) or amniocentesis. These tests carry an elevated risk of miscarriage and are only performed later in pregnancy. Initial screening with NIPT can help to avoid this potentially unnecessary and invasive testing.

There is no risk to the mother or baby, and this test provides the earliest testing available. The technology behind the NIPT test allows for highly accurate results with detection rates for the three most common trisomy conditions present at birth (Down Syndrome, Edwards Syndrome and Patau Syndrome) of over 99%. But it's important to understand that non-invasive prenatal tests such as NIPT Tests are classified as screening tests. This means that they do not test with 100% accuracy, such as with an invasive diagnostic procedure such as amniocentesis.

What is NIPT testing?

Our DNA carries all the genetic information we require for normal health and development. It exists in our cells as 23 pairs of chromosomes. During pregnancy, chromosomal abnormalities can arise in the developing baby as a result of incorrect egg or sperm formation, or during the earliest stages of the baby's development. These chromosomal abnormalities can significantly affect a baby's health and well-being, and it is important to identify any abnormalities as early as possible. NIPT delivers a clear positive or negative result for chromosomal abnormalities, where an extra copy of one chromosome is present (Trisomy). Down syndrome, the most common chromosomal abnormality can be detected with an accuracy rate of >99,9%.

When do doctors recommend the test?

  • Maternal age 35 years or older at delivery
  • Contraindications for invasive prenatal testing, such as placenta prevail, risk of miscarriage, HBV infection etc.
  • History of a prior pregnancy with a chromosomal abnormality
  • Fetal ultrasonographic findings indicate an increased risk of T21, T18 or T13
  • Requires reassurance following previous screening result
  • Received IVF Treatment or has previously suffered from habitual abortion

Sample Required for this testing:

Standard Biological The NIFTY Non-Invasive Prenatal Testing  NIPT Samples: 10 ML Blood

Accuracy of this Test:

The Non-Invasive Prenatal Testing NIPT accuracy is 99%.

Reporting Time:

Results will take 8-10 working days

NIPT Test cost:

A standard Non-Invasive Prenatal Testing NIPT Blood Test cost you 10000/- INR, meanwhile, NIPT Twins is 13000 Rs. Alternatively, we provide NIPT Microdeletions is 26000 Rs.

Why Choose DNA Labs India?

DNA labs India's Non-Invasive Prenatal Testing NIPT follows with dual testing for 100% accuracy when determining this Test.

  • We are the leading lab for Non-Invasive Prenatal Testing NIPT in India
  • Greater Accuracy
  • Collection centres across India
  • Outstanding customer service
  • Strict privacy and confidentiality assured
  • Full-service laboratories providing testing for use in complex cases

Different between Illumina and Ion torrent:

The clinical performance of two massively parallel shotgun sequencing (MPSS) NIPT methods using either an optical NGS technology (Illumina) or a semiconductor NGS technology (Iontorrent ThermoFisher) in high risk and baseline risk pregnancies for the detection of trisomies 21, 18, 13, and monosomy X. It appears clear from most clinical studies that, for the detection of any of the three main trisomies (T13, T18, and T21), the two index tests do not differ (upper 99% confidence interval limit of the difference) by more than 2.6% in clinical sensitivity, 0.64% in clinical specificity, 0.64% in FPR, and 0.65% in ACC. In terms of PPV and NPV, in high-risk pregnancies, index tests differed by less than 6.41% for PPV and 0.33% for NPV. In pregnancies with baseline risk, only the NPV could be reliably estimated and it did not differ (upper 99% confidence interval limit of the difference) by more than 0.33% between the two index tests.

Frequently Asked Questions

  • What is the cost of NIFTY Non-Invasive Prenatal NIPT Test?

    Cost of NIFTY Non-Invasive Prenatal NIPT Test is 10000 Rs

    NIFTY Non-Invasive Prenatal NIPT Test Price in India ₹ 10000
  • What is NIPT Test?

    NIPT Test is a safe, simple, non-invasive prenatal test that detects Down Syndrome, Edward Syndrome, Patau Syndrome

  • What does NIPT screen for?

    NIPT screen for the most common chromosomal disorders: 

    Trisomy 21 (Down syndrome)

    Trisomy 18 (Edwards syndrome)

    Trisomy 13 (Patau syndrome)

  • When is NIPT done in a pregnancy?

    NIPT can be performed any time after 10 weeks into your pregnancy earlier than any other prenatal screening or diagnostic test. 

  • How accurate is NIPT?

    NIPT is 99.9% accurate

  • Should you get NIPT?

    NIPT is recommended for women at high risk of carrying a baby with a chromosomal abnormality like moms-to-be who are 35 or older and previously had a child with a genetic disorder.

  • What is the difference between Iontorrent and Illumina?

    Iontorrent covers depth up to 30x of data whereas Illumina covers the 80-100x depth data

  • What is the cost of NIPT Test?

    NIPT Test Costs 10000 Rs

  • How many days will it take for reports?

    Reports will take 7 working days

₹10,000.00 ₹18,000.0044% off

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