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TDL (Previous Harmony ) VeriSeq v2 NIPT Test

TDL (Previous Harmony ) VeriSeq v2 NIPT: Advanced Prenatal Testing for Reliable Genetic Insights

Get the most proven NIPT test for your baby’s health and peace of mind. HARMONY TEST USED TO BE THE GOLD STANDARD IN NIPT Introduced in 2013, it gained popularity quickly among UK healthcare providers. In recent years, Harmony has lagged behind other NIPT technologies. This has resulted in TDL – the lab providing the test, discontinuing the test across the UK. END OF AN ERA… TDL Genetics ends Harmony NIPT provision after a decade. With outdated technology, high no-call rates, and fierce competition, Harmony loses its shine. As leading NIPT providers, we’re reviewing TDL’s new offering. TDL ( Previous Harmony ) NIPT Illumina VeriSeq v2 The Illumina VeriSeq v2 prenatal test is a new non-invasive prenatal screening test (NIPT) which can be performed from 10 weeks of gestation. The test is a simple blood test taken from the mother, which is then analysed for fetal cell-free DNA (cfDNA). cfDNA is the result of the natural breakdown of fetal cells and can be found in the mother’s blood. Illumina VeriSeq v2 is much more accurate than first-trimester blood screening and ultrasound tests When it comes to prenatal screening, prenatal harmony screening is one of the most validated TDL (Previous Harmony ) VeriSeq v2 NIPT blood tests that look at the fetal DNA fragments in your blood to detect chromosome conditions as early as 10 weeks precisely. The TDL (Previous Harmony ) VeriSeq v2 NIPT test is available at the Miracle Inside Diagnostic Service near Bradford from 10 weeks of pregnancy. It is crafted to fit your protocols and give you peace of mind when you need it most. Our service includes the TDL (Previous Harmony ) VeriSeq v2 NIPT  blood test, allowing you to see your baby in the comfort of our first-class facilities. TDL (Previous Harmony ) VeriSeq v2 NIPT  test costs at Miracle Inside, Leeds, are affordable to fit your budget. An Optional extra ultrasound scan is offered for Only viability (heartbeat) and gestation measurements for people who have not had an early scan with the NHS and don't know how many weeks pregnant. Book the best private TDL (Previous Harmony ) VeriSeq v2 NIPT  test for  £400
  • (A Quick Viability Scan is offered till 15 weeks of Pregnancy for an optional extra £50 )
To secure your appointment at Miracle Inside Diagnostic Scan Centre, the following payments are required:
  • Deposit: A non-refundable deposit of £30.
  • Phlebotomy Charges: An additional fee of £25 is charged for phlebotomy services and the DHL courier service to timely deliver the blood to the laboratory.
These payments must be made when booking to confirm your appointment. The remaining balance for your services can be paid through our website after your appointment. This ensures a smooth and efficient process for both our staff and patients. For any questions or assistance regarding payment, don't hesitate to get in touch with our customer service team at 01134608760 Please click here to book the NIPT Test along with an Ultrasound scan appointment Book Your TDL (Prvious Harmony  NIPT Blood test). Today

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When should you take it? From 10 weeks of Pregnancy How accurate is the TDL (Previous Harmony ) VeriSeq v2 NIPT test?
  1. 99% accurate for Down syndrome,
  2. 97% accurate for Edward’s syndrome,
  3. 80% accurate for Patau syndrome.
Can I find out the gender of my baby?
The purpose of the Illumina VeriSeq v2 test is primarily for the detection of Trisomy 21, 18 and 13. However, you can request X and Y analysis, providing over 99% accuracy for your baby’s gender and Sex chromosomes NOTE: Due to the current COVID situations all Send Away blood will have a surcharge of £10 for next-day delivery by courier to avoid delay in the sample reaching the laboratory.
TDL (Previous Harmony ) VeriSeq v2 NIPT  Prenatal NIPT - An Overview
According to the International Society for Prenatal Diagnosis (ISPD) and the American College of Medical Genetics and Genomics (ACMG),  Non-Invasive Prenatal Testing (NIPT) is a primary prenatal screening blood test for pregnant women of all ages. It is a method that determines whether the fetus will be born with genetic abnormalities. The NIPT Blood test serves as a first-line screen for the diagnosis of chromosome abnormalities. Infants born to mothers above 35 years of age are more likely to have Down Syndrome and other chromosomal conditions. NIPT also detects microdeletion syndromes that occur in infants regardless of their mother's age. TDL (Previous Harmony ) VeriSeq v2 NIPT is the cell-free DNA-based non-invasive prenatal test that screens for specific genetic conditions in a pregnancy as early as 10 weeks of gestation. Miracle Inside Diagnostic Centre near Harrogate provides TDL (Previous Harmony ) VeriSeq v2 NIPT  Genetic Testing, which is a proven NIPT blood test that delivers high-quality and reliable results. It has a 99% detection rate for Down Syndrome and will also identify most cases of Edward Syndrome and Patau Syndrome. Who is it suitable for? The TDL (Previous Harmony ) VeriSeq v2 NIPT Test is suitable for any pregnant woman with a singleton or twin pregnancy (except donor twin pregnancy). Typically, the test is useful for the following patients: Women over 35 who are concerned about their age-related risk of Down Syndrome and other Trisomies. Women under 35 who want a safe, reliable, early, and accurate test for Down Syndrome Women who have an increased risk or “High Risk” result from a Combined Test or Nuchal Translucency scan but wish to avoid unnecessary CVS or amniocentesis, and their risk of miscarriage. Women who have an increased risk or “High Risk” result from a Triple test or Quad test but wish to avoid unnecessary CVS or amniocentesis and the risk of miscarriage. Women with a previous pregnancy with a baby with Down Syndrome, please contact us for info, Patau Syndrome or Edward Syndrome The test is not suitable for multiple pregnancies with donor eggs. Contact us for more information on these TDL (Previous Harmony ) VeriSeq v2 NIPT  blood tests with Ultrasound. Please call 📞 01138301371 to speak with the Healthcare Professional.

Why do we think the Illumina VeriSeq is superior to the Harmony?

  • Better detection rates for all 3 trisomies (> 99%) – Harmony is 99% for trisomy 21, 97% for trisomy 18, & 93% for trisomy 13.
  • Only 1% of samples will fail in processing – Harmony has a 4% failure rate.
  • Shorter turnaround times (Usually 3 – 4 working days) – Harmony is 5 – 7 working Days.
  • PPV (positive predictive value) same as the Harmony Test.
  • American-originated test analysed by the largest NIPT Lab in the UK (TDL Genetics) – one of the only Labs with UKAS accreditation for NIPT testing (same as Harmony test) – other laboratories often do not have UKAS accreditation for NIPT testing.
Gender Confirmation The earliest you can have a scan to know Baby’s Gender is around 16 weeks, and the NHS don’t tend to provide gender confirmation until 20 weeks. A NIPT test can be performed from as early as 10 weeks, with the results arriving in 7 working days. What do about my Regular NHS 12-week scan and NT measurement scans? If you are having an NIPT Test or you have got a negative or Low-risk result on the Non-Invasive Prenatal Test, even then you should not miss your regular 12-week NHS scan and the NT measurements. What if the sample fails? Statistically, the failure rate is 3 % to 4%. If there is not enough cell-free DNA in the blood sample to analyse, we will again take a new sample at no extra cost. What if I have a high BMI? There is a high chance of getting inconclusive results as women with high BMI have a reduction in the proportion of cell-free fetal DNA. To speak to our healthcare professional about TDL (Previous Harmony ) VeriSeq v2  NIPT, call us at  📞 01138301371. Additional Information: NIPT can not be done for multiple gestation pregnancies with 3 or more fetuses. It is also not recommended for pregnant women with a history of bone marrow transplantation or other illnesses. For more clarification, please contact us. We will require details of your GP/Health Care Professional, which may be requested before or at the time of the scan. This scan requires access to the area of interest; it is recommended to wear loose clothing to facilitate this process. Blood results require interpretation, and all results should be shared with your regular healthcare professional / GP, / Fertility specialist. All of our first-line ultrasound scans & health Blood tests are optional. You must be at least 16 years old with no existing medical condition or treatment pending that relates to the scan/blood test you are booking. In case you have any doubts, please check with your GP. Genetic counselling is not provided as part of this Blood test Service. The customer's regular Healthcare professional / GP / Fertility specialist is responsible for ensuring appropriate counselling is provided to the patient.

Frequently Asked Questions (FAQs)

What is the Harmony NIPT test?

The Harmony NIPT (Non-Invasive Prenatal Test) is a safe blood test taken from the mother that analyses cell-free fetal DNA in the bloodstream to screen for certain chromosomal conditions in pregnancy.


What conditions does the Harmony NIPT screen for?

The test primarily screens for:

  • Down syndrome (Trisomy 21)

  • Edwards syndrome (Trisomy 18)

  • Patau syndrome (Trisomy 13)

These are the most common chromosomal conditions screened during pregnancy.


What do these conditions mean?

  • Down syndrome (Trisomy 21) may be associated with learning difficulties, congenital heart defects, and other medical conditions.

  • Edwards syndrome (Trisomy 18) and Patau syndrome (Trisomy 13) are severe conditions linked to high miscarriage rates and serious birth defects. Most affected babies do not survive beyond infancy.


When can the Harmony test be done?

The test can be performed from 10 weeks of pregnancy onwards, making it an early screening option.


How is Harmony different from standard NHS screening?

Unlike traditional screening, which combines blood markers and ultrasound measurements, Harmony analyses fetal DNA directly, making it more accurate for detecting Trisomy 21, 18, and 13.


Can the test tell my baby’s sex?

Yes. With optional X and Y chromosome analysis, the test can determine fetal sex with over 99% accuracy.

  • This option is also available for twin pregnancies

  • In twin pregnancies, a female result applies to both babies; a male result indicates one or both babies are male


Can the test screen for sex chromosome conditions?

Yes, as an optional extra, the test can assess the risk of sex chromosome conditions such as:

  • Turner syndrome (Monosomy X)

  • Triple X syndrome (XXX)

  • Klinefelter syndrome (XXY)

  • Jacobs syndrome (XYY)

  • XXYY syndrome

This option will be discussed during your appointment. Please note that sex chromosome screening is not available for twin pregnancies.


What does a HIGH-RISK result mean?

A high-risk result means there is a strong likelihood that the fetus may have a chromosomal condition.

  • Detection rates exceed 99% for Trisomy 21, 98% for Trisomy 18, and around 80% for Trisomy 13

  • A high-risk result does not confirm a diagnosis

  • Follow-up diagnostic tests, such as CVS or amniocentesi,s are recommended to confirm the result


What does a LOW-RISK result mean?

A low-risk result means it is unlikely that the fetus has Trisomy 21, 18, or 13. While no screening test is 100% accurate, the likelihood of these conditions is very low. Routine pregnancy scans should continue as normal.


How long do results take, and can the test fail?

Results are usually available within 7 working days.
In some cases, the test may fail due to low fetal DNA levels (below 4%). This can occur due to:

  • Early testing
  • High maternal BMI
  • Sampling issues
  • Certain fetal conditions

If this happens, a repeat blood test is offered at no extra cost.


Is the Harmony test safe for my pregnancy?

Yes. The test is non-invasive and involves only a blood sample from the mother’s arm. There is no risk of miscarriage, unlike invasive tests such as CVS or amniocentesis.


Is the Harmony NIPT available on the NHS?

The NHS currently offers only combined or quadruple screening tests, and invasive testing is offered if those results are high risk.
NIPT is not routinely available on the NHS due to cost, which is why many parents choose private testing for greater accuracy and peace of mind.


To secure your appointment at Miracle Inside Diagnostic Scan Centre, the following payments are required:

  • Deposit: A non-refundable deposit of £30.
  • Phlebotomy Charges: An additional fee of £35 is charged for phlebotomy services and the DHL courier service to timely deliver the blood to the laboratory.
These payments must be made when booking to confirm your appointment. The remaining balance for your services can be paid after your appointment at our clinic. This ensures a smooth and efficient process for both our staff and patients.
The Appropriate cancellation charge will apply as shown below.
  • Amendments: 72 hrs ( 3 days Notice )
  • Bookings made on the same day or 1 to 3 days before your appointment cannot be amended.
  • Refund Applicable: 14 Days or more: Full refund
  • Between 10 and 14 days: £30 non-refundable deposit balance paid will be refunded
  • Between 1 and 9 days: No refund will be given
  • Failure to attend: No refund will be given
  • Rescheduled Appointments are not eligible for Cancellation or Refunds.
Here are some additional resources that may be useful: - Antenatal Results and Choices (ARC): This is a national charity that provides non-directive support and information to parents before, during, and after antenatal screening. You can visit their website at www.arc-uk.org or call their helpline at 0845 077 2290 or 0207 713 7486. The helpline is open from Monday to Friday, 10 am to 5:30 pm. - Down's Syndrome Association: This association provides support for people with Down syndrome and their families. You can visit their website at www.downs-syndrome.org.uk or call them at 0333 1212 300. They are open from Monday to Friday, 10 am to 4 pm. - Support Organisation for Trisomy 13/18 (SOFT): This organisation provides information and support for families affected by Trisomy 13/18. You can visit their website at www.soft.org.uk. Book an appointment with GODSON JOHNSON using Setmore