At Lumipeek, we provide the most advanced and comprehensive non-invasive prenatal testing (NIPT) available. Our NIPT test is conducted in a state-of-the-art German laboratory, ensuring the highest standards of accuracy and reliability.
Why Choose Lumipeek?
- Free Genetic Consultation: Speak with our geneticists at no cost to get personalized recommendations on the best NIPT test for you.
- Fast Results: Receive your results within 3 to 5 working days.
- High Reliability: Over 99.9% accuracy in detecting the most common trisomies, including Down syndrome.
- Non-Invasive and Safe: 100% safe for both you and your baby.
- Experienced and Trusted: With 15 years of experience and over 100,000 completed NIPT tests.
- Risk-Free: Sample analysis is conducted in a German laboratory
- Privacy Assured: Test results are encrypted and not shared with any healthcare system.
- Gender Determination: Discover your baby’s gender for free with every test option.
- Convenient Online Results: Easily download your results via the internet on your mobile phone or desktop computer.
Our mission is to empower expectant parents with advanced, accurate, and comprehensive genetic insights. Whether you’re seeking reassurance or detailed information, our NIPT services offer unparalleled support for your unique journey.
Lumipeek Advanced NIPT – £350
The Lumipeek Advanced NIPT goes beyond basic chromosome analysis. This test is more than 99.9% reliable for detecting the most common 3 trisomies, including T21, T18 and T13, it also provides other screening option,Sex chromosomes aneuploidies, other autosomal aneuploidies and 8 microdeletion/duplication syndromes
Key Features of Lumipeek Advanced NIPT:
- High Detection Rate: Over 99% accuracy for detecting common trisomies.
- Microdeletions: Identifies key microdeletion syndromes that other tests may miss..
- Versatile Testing: Suitable for any trimester, ensuring flexibility and convenience.
Lumipeek Premium NIPT: Comprehensive Genetic Screening for Your Baby’s Health
Price: £650.00
Available from: 10 weeks of pregnancy
Lumipeek Premium by Geneplanet offers an advanced, non-invasive prenatal test (NIPT) that provides comprehensive genetic screening from the comfort of your home. Processed using the world-class Illumina technology at a state-of-the-art laboratory in Germany, this test offers unparalleled accuracy, safety, and peace of mind. Lumipeek Premium is designed to detect a broad range of genetic anomalies in your baby, including common trisomies and rare microdeletions.
Key Features of Lumipeek Premium
- Early Pregnancy Scan: All NIPT options, including Lumipeek Premium, come with a complimentary early pregnancy scan before the blood draw. This scan ensures accurate dating of your pregnancy and confirms that you are at least 10 weeks pregnant, the minimum gestational age for this test.
- Highly Accurate Genetic Screening: Lumipeek Premium tests for a wide array of chromosomal abnormalities, including trisomies T21 (Down Syndrome), T18 (Edwards Syndrome), and T13 (Patau Syndrome), as well as other serious genetic conditions like microdeletions and sex chromosome aneuploidies.
- Comprehensive Screening Options:
- Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome), and Trisomy 13 (Patau Syndrome)
- Expanded Autosomal Trisomies: Screening of all 22 pairs of chromosomes for additional trisomies.
- Sex Chromosome Aneuploidies (Optional): XO (Turner Syndrome), XXY (Klinefelter Syndrome), XYY (Jacob Syndrome), XXX (Triple X Syndrome).
- Fetal Sex/Gender Identification (Optional): Discover whether your baby is a boy or a girl with a simple, non-invasive test.
- Microdeletion Syndromes: Testing for conditions like DiGeorge syndrome, Prader-Willi syndrome, Angelman syndrome, and more.
- All Microdeletions and Duplications Over 7 Million Base Pairs: Detecting abnormalities beyond the typical chromosome pairs.
- No Risk to Your Baby: Lumipeek Premium is a completely non-invasive test that analyzes cell-free DNA fragments from your blood. There is no risk to your pregnancy, making it a safe alternative to invasive testing methods like amniocentesis or CVS.
Who Should Consider Lumipeek Premium?
While Lumipeek Premium is suitable for all expectant mothers, it is particularly beneficial for:
- Women over 35 years old
- Those who have undergone IVF or have a history of recurrent miscarriage
- Women with abnormal results from other first-trimester screening tests
- Anyone seeking peace of mind about the genetic health of their baby
What Does the Lumipeek Premium Test Involve?
- Early Pregnancy Scan: Before proceeding with the blood test, an early pregnancy scan ensures you are at least 10 weeks pregnant. This is crucial for obtaining accurate results.
- Blood Draw: A simple blood draw is taken from your arm, and the sample is then sent to our certified German laboratory for analysis.
- Analysis: Your DNA sample is processed using Illumina’s VeriSeq NIPT Solution v2 platform, a next-generation sequencing (NGS) technology that allows for highly accurate screening of your baby’s genetic health.
- Results: You will receive your results within 5-7 working days. If there is insufficient fetal DNA in the blood sample, a repeat test may be required at no additional cost.
What Can You Expect from Your Results?
Lumipeek Premium provides a detailed report, including:
- Chromosomal Anomalies: Results for trisomies, sex chromosome aneuploidies, and expanded autosomal trisomies.
- Microdeletions: Screening for a broad range of microdeletion syndromes.
- Fetal Sex (Optional): If selected, the gender of your baby will be included.
- Genetic Counseling: If you receive unexpected or concerning results, we offer complimentary genetic counseling to help you understand your options and next steps.
How Accurate Is Lumipeek Premium?
- Sensitivity: The ability to correctly identify a fetus with a specific condition.
- Specificity: The ability to correctly identify a fetus without a condition.
- Positive Predictive Value (PPV): The probability that a positive test result indicates the presence of a condition.
- Negative Predictive Value (NPV): The likelihood that a low-risk result means your baby is free from the condition.
Please note that while Lumipeek Premium provides highly accurate screening, it is a screening test, not a diagnostic test. This means that it can help identify the risk of genetic conditions, but it does not guarantee a diagnosis. If your test result is positive, further diagnostic testing, such as amniocentesis, may be required to confirm the condition.
Why Choose Lumipeek Premium?
- Advanced Technology: Utilizes Illumina’s cutting-edge next-generation sequencing platform.
- Comprehensive Screening: Offers one of the most thorough genetic screening options available, covering a wide range of potential conditions.
- Safe and Non-Invasive: The test poses no risk to you or your baby, unlike invasive tests such as amniocentesis.
- Rapid Results: Expect your results within 5-7 working days, allowing you to make informed decisions about your pregnancy.
Frequently Asked Questions
1. Do I need to be over 10 weeks pregnant?
Yes. Lumipeek Premium requires a minimum of 10 weeks of pregnancy. We will perform an ultrasound to confirm this before proceeding with the blood draw.
2. How will I receive my results?
Your results will be communicated by phone, followed by a detailed email with your NIPT report for your records.
3. Can I find out the sex of my baby?
Yes, Lumipeek Premium offers optional fetal sex determination, which is available for singleton pregnancies
4. What happens if there isn’t enough fetal DNA?
In rare cases, the fetal DNA sample may be insufficient. If this happens, a repeat blood test is offered at no extra cost.
5. Can I get counselling if my results are unexpected?
Yes, we provide access to complimentary genetic counselling to guide you through the next steps after receiving your results.
Additional Information
While NIPT provides a high level of accuracy, it is important to remember that it is a screening test and not a definitive diagnostic test. It is designed to help identify potential genetic concerns early in pregnancy, but further diagnostic tests may be recommended if any concerns arise. Always consult your healthcare provider to discuss the results and decide on the best course of action for you and your baby.
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