Identifai Genetics – Prenatal testing is about to change

A new standard in prenatal testing is about to be born…

The challenge

Millions of babies are born every year with severe genetic diseases.

Existing non-invasive screening methods allow the detection of less than 10% of known genetic disorders. Invasive genetic tests are risky, late, and thus rarely used.

10% disorders detected today

Undetected

Solution

Cell free DNA is circulating in maternal blood

Identifai’s technology enables the isolation, examination and analysis of the fetus’s cell free DNA

Identifai’s novel paradigm and digital solutions allow early, non-invasive and comprehensive prenatal genetic testing

Technology

Identifai’s cutting edge bioinformatics technology offers an early and comprehensive prenatal screening test for genetic syndromes. Using a simple blood test from the mother during the first trimester of the pregnancy, our proprietary data science algorithms provide a high-resolution yet comprehensive perspective of the fetus’s health at an early stage of the pregnancy.

How does it work?

1. A blood draw is taken from the mother

2. The sample is sequenced – fetal and maternal DNAs are still mixed

3. Fetus’s DNA is digitally isolated using Identifai’s computational process

4. Fetus’s DNA is reconstructed at high resolution, and actionable variants (mutations) are located and analyzed

5. A genetic report is generated

Current solutions

Current technologies are either invasive, e.g. amniotic fluid test, or limited to only ~10% of genetic conditions, mainly chromosomal abnormalities.

Detect chromosomal conditions

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Our solution

Identifai’s technology offers the only available clinical solution for an early, non-invasive and comprehensive prenatal genetic screening, from point mutations to chromosomal anomalies.