Next-Generation NIPT

Clarifi NIPT

Next-Generation Non-Invasive Prenatal Testing

Overview

Clarifi NIPT is our most advanced non-invasive prenatal screening test. Powered by the latest sequencing technology, Clarifi provides comprehensive screening for a wide range of genetic conditions with unparalleled accuracy — all from a simple maternal blood draw.

100+

Conditions

99.5%+

Accuracy

From Week

5–7 Days

Results

What Clarifi Screens For

Common Trisomies

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

Rare Trisomies

Screening for less common chromosomal abnormalities across all 24 chromosomes

Sex Chromosome Aneuploidies

Turner syndrome, Klinefelter syndrome, Triple X, and XYY

Microdeletions

22q11.2, 5p15, 1p36, and other clinically significant microdeletion syndromes

Single Gene Disorders

Selected autosomal dominant and recessive conditions

Fetal Fraction Analysis

Quality metrics to ensure reliable results

How It Works

Counseling

Pre-test genetic counseling to understand your options and what to expect

Sample Collection

A simple blood draw at any of our partner hospitals or via home service

Advanced Analysis

Your sample undergoes comprehensive genomic analysis in our lab

Results & Support

Detailed results with post-test counseling from our genetic counselors

Frequently Asked Questions

What makes Clarifi different from other NIPT tests?

Clarifi uses the most advanced sequencing technology to screen for over 100 conditions, far more than standard NIPT tests that only screen for common trisomies.

How early can Clarifi be performed?

Clarifi can be performed from 9 weeks of pregnancy, earlier than many other NIPT tests.

Is Clarifi suitable for twin pregnancies?

Yes, Clarifi can be used for twin pregnancies, though the range of conditions screened may vary.

What is fetal fraction and why does it matter?

Fetal fraction is the amount of fetal DNA in the mother's blood. A minimum fetal fraction is needed for accurate results — our test includes this quality check.

Can Clarifi replace diagnostic tests like amniocentesis?

Clarifi is a screening test, not a diagnostic test. Positive results should be confirmed with amniocentesis or CVS.

Choose Clarifi for Comprehensive Screening

Get the most complete picture of your baby's genetic health

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