Packages include Whole Exome Sequencing, Genotyping, DNA Methylation, Hereditary Cancer Screening, Carrier Screening, Health Risks Assessment, Ancestry Insights, Customized Wellness Planning, Pharmacogenetics and More.
✅ Secure, Private and Confidential Screening
✅ Personalized Health Insights and Recommendations
✅ Easy to Read Illustrative Reports by Email
✅ Complimentary Consultation with Geneticists
✅ Clinician-Assisted Specimen Collection at Clinics or Home
Unveil Your DNA: Discover the Secrets Within
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Confirm the paternity of your unborn baby with a 99.9% accurate test that requires only blood samples from the mother and alleged father
A Paternity DNA Test is used to determine who is the genetic Father of a Child or Children
Carrier screening for Monogenic disease
Thalassemia mutations detection for > 508
Thalassemia mutation including common
Alpha- and Beta-thalassemia
Newborn genetic screening for 112 genetic
diseases
Newborn metabolic disorders screening
Clinical whole exome sequencing for detection
and diagnosis of rare diseases
Non-invasive early screening of colorectal
cancer by detecting 3 Methylation marker
genes
Examining the genetic code to analyze individual characteristics lifestyle, design balancing food and nutrition including the exercise that is most appropriate for you. It can also predict the risk of diseases that will be caused by genetic factors to be used as information to reduce the risk of disease in the future.
Detection of gene mutations that result in a
higher-than-normal chance of developing
cancer which can help predict the risk of
cancer.
Measurement of telomere length to determine
your true biological age
Explore Your Ancestry, Optimize Your Health, and Embrace Your Unique Genetic Traits with Our Comprehensive DNA Testing Service
This is a medical test that couples or individuals planning to have a baby can undergo before conception. It is designed to identify potential genetic disorders in the baby's DNA. The primary goal is to provide reliable and early information about the fetal genetic health without resorting to invasive procedures that might carry the risk of miscarriage. This test helps parents make informed decisions about their pregnancy and prepares them for any potential health challenges their child may face.
SENTIS Hereditary Cancer Screening is a specialized DNA test that focuses on detecting genetic mutations associated with hereditary or familial cancers. This test helps individuals understand their genetic predisposition to certain types of cancer. By analyzing an individual's genetic blueprint, SENTIS aims to provide early insights into the risk of developing hereditary cancers. Armed with this knowledge, individuals can take proactive measures for cancer prevention and early detection, potentially saving lives.
Hereditary DNA testing is a comprehensive examination of an individual's genetic makeup. By analyzing an individual's DNA, this test offers insights into one's unique genetic blueprint. It can reveal information about ancestry, traits, and potential health risks, including genetic predispositions to various conditions. This test empowers individuals to gain a deeper understanding of themselves on a genetic level, which can be valuable for making informed decisions about their lifestyle, health, and wellness.
Genetic testing is a broad category of medical and scientific examinations that involve analyzing an individual's DNA. These tests can reveal information about an individual's genetic makeup, including their susceptibility to certain diseases, ancestry, and genetic traits. Genetic testing has applications in various fields, such as medicine, ancestry research, and personalized healthcare. It helps individuals and healthcare providers make informed decisions regarding health, family planning, and overall well-being.
Frequently Asked Questions
Genetic disorders arise due to alterations in an individual's genetic material, encompassing their genes and chromosomes. Aneuploidy characterizes a condition where there are either surplus or deficient chromosomes. Trisomy denotes the presence of an extra chromosome, while monosomy signifies the absence of one chromosome. Inherited disorders, conversely, result from genetic changes termed mutations. These disorders comprise conditions like sickle cell disease, cystic fibrosis, Tay-Sachs disease, and numerous others. Typically, for an offspring to be affected by an inherited disorder, both parents must carry the same mutated gene.
Prenatal genetic testing is a medical examination performed during pregnancy to assess the genetic health and development of the fetus. It aims to identify potential genetic abnormalities, chromosomal disorders, or inherited conditions in the unborn child. Prenatal genetic testing offers valuable information to expectant parents and healthcare providers, aiding in making informed decisions about the pregnancy, including choices about the continuation of the pregnancy, preparing for medical interventions, or planning for the care of a child with special needs.
1. Screening Tests: Prenatal screening tests are typically the first step in assessing the risk of a fetus having a genetic disorder. These tests are non-invasive and include options like non-invasive prenatal testing (NIPT), maternal serum screening (also known as triple or quad screen), and ultrasound examinations. They provide information about the likelihood of the fetus having certain genetic conditions. If a screening test suggests an increased risk, further diagnostic testing may be recommended.
2. Diagnostic Tests: Prenatal diagnostic tests are more invasive and definitive. They are performed when a screening test indicates a higher risk of a genetic disorder or when there are other indications for a diagnostic assessment. Common diagnostic tests include chorionic villus sampling (CVS) and amniocentesis. These tests directly examine the genetic material of the fetus, providing a definitive diagnosis of genetic conditions, chromosomal abnormalities, or other genetic disorders.
Embark on a unique journey of self-discovery with our DNA testing services. Uncover your ancestral origins, gain insights into your health, and explore the fascinating world of your genetic traits. Your DNA holds the key to your past, present, and future, and we're here to help you decode it.
Empower yourself with personalized genetic insights. Our DNA testing service offers a window into your genetic makeup, helping you make informed decisions about your health and lifestyle. It's time to take control of your destiny and embrace the power of your DNA.
Unveil the mysteries of your genetic code with our cutting-edge DNA testing. Gain valuable knowledge about your ancestry, health predispositions, and unique traits. Armed with this information, you can make proactive choices for a healthier and more fulfilling life.
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Last updated: June 30th, 2022
If you’re dissatisfied with a purchase, We invite You to read our refund and return policy. The following conditions apply to any items or services that you bought from Us.
The meanings of words with the first letter capitalized are defined as follows. The following definitions shall have the same meaning regardless of whether they appear in singular or plural.
For the purposes of this Refund and Return Policy:
You are entitled to cancel Your Order for Packages as per the following terms:
3.1 If you cancel an Order before 4 PM (GMT+7) the next day after making the payment, you can receive an 80% refund. For example, if you want to cancel your reservation, for example, after making it on March 25th, 2022 at 10 AM; You may do so and receive an 80% refund if you notify the company before 4:00 PM on March 26th, 2022.
3.2 If you cancel an Order before 4 PM (GMT+7) one day before the appointment date, you will receive a 50% refund. For example, if you scheduled a lab test for March 29th at 10 AM, you may cancel and receive a 50 percent refund if you notify the laboratory by 4 PM on March 28th, 2022.
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