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Health and WellnessGenome Sequencing
Genome Sequencing – Unraveling the Code of Life
Gain a complete understanding of your DNA with our advanced Genome Sequencing service. From inherited conditions to health risks and drug responses, this test empowers you with actionable genetic insights.
Our Comprehensive Genomic Solutions
Empowering Precision Medicine with In-Depth Genome Analysis
Our Genome Sequencing service maps all 20,000+ genes in your DNA, helping detect mutations, assess hereditary diseases, and tailor healthcare plans. Whether you’re managing a chronic condition or planning for the future, genetic clarity starts here.
Book an Appointment
Online appointment process makes it easy for you to book for any one of our services.
Key Benefits of Our Genome Sequencing Offers
Inherited Condition Detection
Identify genetic predispositions and inherited mutations associated with various health issues and their potential impact on well-being.
Drug Response Insights
Discover how your genes impact medication effectiveness, personalize treatments, and reduce the risk of adverse drug reactions with genetic insights.
Predictive Health Planning
Predict potential chronic disease risks in advance and take proactive steps early to prevent health issues before they develop.
Personalized Treatment Guidance
Empower your doctors to deliver personalized medical care precisely aligned with your unique genetic makeup for more effective treatment outcomes.
We offer a highly testing solution for Genome Sequencing
If you are a patient:
Visit a physician or contact us to talk to one of our Clinical Virologists to choose the right test for you. All orders must be made by a physician.
If you are a physician:
Explore Our Advanced Immunogenetics Solutions
Frequently Asked Questions!
It reads and analyzes the entire DNA sequence to identify genetic variations and mutations.
Genetic disorders, inherited diseases, cancer mutations, and rare conditions can be identified through genome sequencing.
Yes, it guides personalized treatments by identifying individual genetic variations affecting disease and drug response.
Data privacy concerns, uncertain findings, and limited interpretation for some genetic variants are potential limitations.
Non-Invasive Prenatal Testing/Screening
Pre-Implantation Genetic Testing/Screening (PGT/PGS)
Male/Female Fertility
Rapid Prenatal & Pregnancy Loss
Maternal Cell Contamination (MCC)
Product of Conception (POC)
My HLA (Human Leucocyte Antigen)
Comprehensive Oncology Screening
Breast Cancer Screening (BRCA)
Cervical Cancer Screening
Prostate Cancer Screening
Heredity Cancer Panel
Leukemia Panel
Lymphoma Panel
Carrier Screening
Newborn Screening
Infectious Diseases Screening
Rare Diseases Screening
Consumer Genomics
Gut Metagenomics
Metagenomics
Personalized Medicine