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Clear answers to questions that matter.

The Harmony Prenatal Test is a blood screening test for trisomies 21 (Down syndrome), 18, and 13 that delivers accurate results from as early as 10 weeks of pregnancy.

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Demand Clarity

Harmony delivers exceptional accuracy with detection rate greater than 99% and a low false positive rate of less than 0.1% for trisomy 21 screening.1

For Pregnant Women*

Proven accuracy in pregnant women of any age or risk.

Targeted Technology

Harmony uses a unique DNA-based method to achieve exceptionally precise results.

* Both under 35 and over 35 age groups, studies have included women ages 18-48.
1. Norton et al. N Engl J Med. 2015 Apr 23;372(17):1589-97

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The Harmony® Prenatal Test was developed by Ariosa Diagnostics (San Jose, California, USA). The Harmony® reagents and Ariosa cell-free DNA System (AcfS) software used as part of the Harmony Prenatal Test are CE Marked under the IVD Directive 98/79/EC. Harmony is a non-invasive prenatal test (NIPT) based on cell-free DNA analysis. NIPT is intended for prenatal screening and is not intended to be the sole basis for diagnosis. Harmony test results are intended to be used in conjunction with other clinical and diagnostic results according to professional practice, including confirmatory fetal diagnostic tests, parental evaluation, clinical genetic counseling and counseling, as appropriate. Harmony does not screen for potential chromosomal or genetic conditions other than those expressly identified in this document. Before making any treatment decisions, all women should discuss their results with their healthcare provider, who can recommend confirmatory, diagnostic testing where appropriate.

HARMONY and HARMONY design are trademarks of Ariosa Diagnostics, Inc. in the US. HARMONY is a trademark of Roche in other countries. All other trademarks are the property of their respective owners.

Copyright © 2022 Life Genomics. All rights reserved.

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