The Most Extensive NIPT Panel for Fetal Chromosomal Abnormalities
In-depth insights for a wide spectrum of chromosomal abnormalities
DNA GTx’s NIPT Plus analyzes fetal cell-free DNA (cfDNA) from maternal blood to screen for all autosomal aneuploidies (chromosomes 1–22), sex chromosome aneuploidies, and a broad range of common copy number variations (CNVs). This panel also provides accurate fetal sex determination. As the most comprehensive minimally invasive prenatal screening available, it enables early detection of a wide spectrum of genetic conditions, empowering expectant parents and healthcare providers with detailed information for informed prenatal care.
Who is this test for?
- Expectant parents who want the most detailed genetic screening available
- Pregnancies with increased genetic risk due to family history, age, or ultrasound findings
- Parents who want to maximize early detection of potential conditions
- Individuals seeking greater peace of mind with a thorough prenatal checkup
What it Screens for
- Autosomal Aneuploidies:
- All chromosomes 1 to 22
- Sex Chromosome Aneuploidies:
Monosomy X (Turner Syndrome)
- Monosomy X occurs when one X chromosome is missing in females, leading to short stature, infertility, and possible heart or kidney issues. Some cases present in mosaic form with milder features.
Triple X Syndrome
- Triple X Syndrome occurs when there's an extra X chromosome, often causing taller stature and mild learning or developmental differences in females.
Klinefelter Syndrome
- Klinefelter Syndrome occurs when there''s an extra chromosome, often causing taller stature, reduced fertility, and mild learning differences in males.
XYY Syndrome
- XYY Syndrome occurs when there's an extra Y chromosome, causing taller stature and mild learning or developmental differences.
- Copy Number Variations (CNVs):
- 139 common microdeletions and microduplications associated with genetic disorders
- Fetal Sex:
- Male or female determination
Key benefits
- Minimally Invasive & Safe: Maternal blood draw only—no risk to mother or baby.
- Broad Genetic Screening: Covers all autosomal chromosomes plus sex chromosomes and numerous CNVs for a comprehensive overview.
- Early and Accurate Detection: Effective from 10 weeks of pregnancy with high sensitivity and specificity.
- Reliable Fetal Sex Information: Helps parents prepare and plan with accurate sex determination.
- Supports Personalized Prenatal Care: Provides detailed genetic insights to guide clinical decisions and reduce invasive testing.
Turn Around Time
- 2 weeks
How it Works
Step 1: Maternal Blood Sample Collection
- A blood sample is taken from the expectant mother.
- This sample contains cfDNA from both mother and baby.
Step 2: cfDNA Extraction
- The cfDNA is carefully separated from the rest of the blood.
- These tiny DNA fragments can reveal genetic changes or risks.
Step 3: Library Preparation
- The cfDNA is prepared so it can be read by our sequencing machines.
- We add special tags and focus on the most important parts of your cfDNA.
Step 4: Whole Genome Sequencing
- Advanced sequencing reads the entire genome at high resolution.
- Provides a comprehensive view of genetic information from cfDNA.
Step 5: Data Analysis
- Our proprietary software (D-KRYPT) helps us understand what the DNA changes mean.
- The results are derived from trusted medical databases.
Step 6: Personalized Patient Report
- You got a clear, easy-to-read report with important findings.
- Your doctor can use this to guide treatment or next steps.
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Offer the Most Comprehensive Prenatal Screening
With DNA GTx NIPT Plus, you can provide expectant parents with the widest genetic coverage available — screening all autosomal chromosomes, sex chromosome aneuploidies, common CNVs, and determining fetal sex
Gain Maximum Insight Into Your Baby’s Health
Safe from 10 weeks of pregnancy and with results ready in 7–10 days, NIPT Plus supports informed decisions, early care planning, and peace of mind for your pregnancy journey.
*All information is handled with strict confidentiality.
