DID YOU KNOW?
DNA holds all valuable information related to your baby! It can tell us not only about hair & eye colour but also about disease risk, immunity & more!
This information becomes more important for NEWBORN
WHY?
About one-third babies & children in ICU have a genetic disorder!
GENETIC TESTING, A POWERFUL TOOL, CAN GIVE PARENTS & DOCTORS
THE RIGHT INFORMATION WHEN TIME MATTERS THE MOST!
A powerful yet simple genetic test for newborns that can be done from the convenience of your home!
WHY GENOME-SCOPE ?
BREAKTHROUGH TECHNOLOGY
Uses Next Generation Sequencing to provide information about your baby’s genes on advanced high throughput Illumina based platform
SIMPLE & CONVENIENT
Requires only a few blood drops from a simple heel prick that can be collected by our paramedic at home
EXTENSIVE COVERAGE
Analyses 4000+ genes related to common & rare disorders that can impact a newborn (cancer, heart, blood, bone, kidney & metabolic disorders & more)
QUICK DIAGNOSIS
Generates detailed reports within 28 days with >95% accuracy
PERSONALISED CARE
Helps you in providing better & personalised care to the baby following early diagnosis
GENETIC COUNSELLING
Offers pre & post-genetic counselling to answer all your doubts, disucss your family history & help you understand the report
WHY GENOME-SCOPE ?
WHY IS GENETIC TESTING
IMPORTANT FOR YOUR BABY?
Your baby’s DNA is unique & any unwanted variations can cause a disease. Genetic testing helps you know all about their DNA & health
Genetic testing can help know the severity of the disease & help you plan better for long-term care & treatment
Babies may appear healthy at birth but may have hidden genetic condition. These diseases can be life-threatening & early diagnosis can make a big difference
Genomic information obtained from the baby may be relevant to siblings & help in planning future pregnancies
HOW DOES THE TEST WORK?
HOW DOES
THE TEST WORK?
WHAT’S THE SCIENCE BEHIND IT?
Although human genome has ~20,000 genes that perform different functions. Genome-Scope collects data on ~4200 clinically relevant genes but with a unique approach!
THUS, MAXIMIZING THE BENEFITS & MINIMIZING THE UNCERTAINTIY!