Cenata GmbH | Paul-Ehrlich-Str. 23 | D-72076 Tübingen | Tel. 07071 – 565 44 430 | Fax 07071 – 565 44 444

Cenata GmbH | Paul-Ehrlich-Str. 23 | D-72076 Tübingen | Tel. 07071 – 565 44 430 | Fax 07071 – 565 44 444

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Fast,
accurate result
Result within an average
of 3 business days
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Excellent
detection rate
>99% detection rate for trisomy 21
in published studies
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Low
false-positive rate
Only 0.06% for trisomy 21
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Highly qualified medical
team for diagnosis
and advice
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For physicians

For expectant parents

For physicians

For expectant parents

The Harmony® Test

The Harmony® Test can reliably detect the risk of the chromosomal disorders trisomy 21trisomy 18trisomy 13 as well as X- and Y-chromosomal disorders. All aspects of the Harmony® Test are carried out according to european standards of quality and data protection.

Expert opinions on non-invasive prenatal screening test (NIPT)

 

Performing Harmony® Test

Advantages of the Harmony® Test

Excellent detection rate for trisomy 21, 18 and 13

Very low false-positive rate

Fast turnaround time

Excellent clinical validation in studies with more than 270.000 patients

Affordable price

Feasibility under heparin treatment

Latest News

Latest publication: Screen-positive rate in cell-free DNA screening for microdeletion 22q11.2

In a recent study, published in February 2023 in Prenatal Diagnosis, we investigated in collaboration with Prof. Kagan (University Women’s Hospital Tuebingen) the correlation between the screen-positive rate and the fetal fraction (proportion of cell-free fetal DNA) when screening for microdeletion 22q11.2 (DiGeorge syndrome). We analyzed own data from more than 50,000 singleton pregnancies. The

Read more »

The Harmony® Test

The Harmony® Test can reliably detect the risk of the chromosomal disorders trisomy 21trisomy 18trisomy 13 as well as X- and Y-chromosomal disorders. All aspects of the Harmony® Test are carried out according to european standards of quality and data protection.

Expert opinions on non-invasive prenatal screening test (NIPT)

Durchführung Harmony Test

Advantages of the Harmony® Test

Excellent detection rate for trisomy 21, 18 and 13

Very low false-positive rate

Fast turnaround time

Excellent clinical validation in studies with more than 270.000 patients

Affordable price

Feasibility under heparin treatment

Latest News

Latest publication: Screen-positive rate in cell-free DNA screening for microdeletion 22q11.2

In a recent study, published in February 2023 in Prenatal Diagnosis, we investigated in collaboration with Prof. Kagan (University Women’s Hospital Tuebingen) the correlation between the screen-positive rate and the fetal fraction (proportion of cell-free fetal DNA) when screening for microdeletion 22q11.2 (DiGeorge syndrome). We analyzed own data from more than 50,000 singleton pregnancies. The

Read more »

The Harmony® Test

The Harmony® Test can reliably detect the risk of the chromosomal disorders trisomy 21trisomy 18trisomy 13 as well as X- and Y-chromosomal disorders. All aspects of the Harmony® Test are carried out according to european standards of quality and data protection.

Expert opinions on non-invasive prenatal screening test (NIPT)

Durchführung Harmony Test

Advantages of the Harmony® Test

Excellent detection rate for trisomy 21, 18 and 13

Very low false-positive rate

Fast turnaround time

Excellent clinical validation in studies with more than 270.000 patients

Affordable price

Feasibility under heparin treatment

Latest News

Latest publication: Screen-positive rate in cell-free DNA screening for microdeletion 22q11.2

In a recent study, published in February 2023 in Prenatal Diagnosis, we investigated in collaboration with Prof. Kagan (University Women’s Hospital Tuebingen) the correlation between the screen-positive rate and the fetal fraction (proportion of cell-free fetal DNA) when screening for microdeletion 22q11.2 (DiGeorge syndrome). We analyzed own data from more than 50,000 singleton pregnancies. The

Read more »

Procedure of the Harmony® Test

Genetic counseling

Patient requests the Harmony® Test and gets a genetic counseling by obstetrician or human geneticist

Blood sample

Blood sample is taken and the order form is filled out by physician and patient

Shipping

Blood sample and order form are sent

Test performance

Test is carried out, data is analyzed and the findings are compiled

Receipt of report

Physician reports the findings to the patient including genetic counseling
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