Genome X Crafting Health, Lifelong Joy & Visionary Future
Genome X is pioneering innovation in Pakistan, revolutionizing healthcare with exclusive tests and cutting-edge global advancements.
What secrets does your DNA hold?
MIT Technology Review paid attention to ‘Genetic Fortune Telling’ in ’10 Breakthrough Technologies 2018’. Genes have all the information you may wish to know. Your genes exactly know your weaknesses, personality, aptitude and even the most effective exercises for you. Start to prepare for the era of the healthy 100-year life through genetic analysis.
Genome X is leading global healthcare innovation
Genome X is a progressive clinical diagnostic laboratory based in Lahore. It offers top-tier Next-Generation Sequencing (NGS) services for the precise diagnosis of cancer and genetic disorders.
Heritage Track
Our Services
Heritage Track
Ancestry Test
At Genome X, our ancestry test allows you to explore your genetic heritage and trace your family’s origins across generations. Using advanced DNA analysis, we provide detailed insights into your ancestral roots, revealing the regions and populations your ancestors came from.
Heritage Track
Paternity Test
At Genome X, we are at the forefront of high-quality, next-generation sequencing (NGS) solutions designed for precision diagnostics. Whether it is for cancer detection, genetic disease diagnosis, or research purposes, our sequencing services provide a deep insight into the genetic makeup of individuals.
clinical diagnostics
Our Services
Non-Invasive prenatal test
NIPT Amity
Genome X Non-Invasive Parental Testing (NIPT) provides a safe and accurate way to assess genetic information without invasive procedures. They are designed to help expectant parents and families understand their genetic risks and make informed decisions about health and pregnancy.
Screening Test
Carrier Screening
Genome X offers advanced carrier screening to help individuals and couples identify their risk of passing on genetic conditions. Our tests detect a wide range of hereditary disorders, even without symptoms. With accurate insights, we empower families to make informed decisions for healthier future generations, making genetic health accessible to all.
Newborn genetic test Subheading
InfantGen scan
Genome X InfantGen Scan helps detect any abnormalities or genetic risks that may require attention, enabling you to make informed decisions and take proactive steps for your baby’s well-being. Genome X supports personalized care by offering early detection, giving you peace of mind.
Precision Medicine
Our Services
Cancer prediction test
Cardic Health
Genome X cardiac health test evaluates genetic predispositions and clinical markers to assess your risk of developing heart-related conditions such as coronary artery disease, arrhythmias, or cardiomyopathies. By identifying these risks early, you can adopt preventive measures, make informed lifestyle choices, and seek timely medical intervention to maintain a healthy heart.
Cancer prediction test
Onco Alert
Genome X Onco Alert test analyzes key genes that influence cancer susceptibility, such as BRCA1, BRCA2, and others linked to Lynch syndrome and familial adenomatous polyposis. Genome X provides clear, actionable insights that can lead to early detection and potentially life-saving interventions.
Newborn genetic test Subheading
InfantGen scan
Genome X InfantGen Scan helps detect any abnormalities or genetic risks that may require attention, enabling you to make informed decisions and take proactive steps for your baby’s well-being. Genome X supports personalized care by offering early detection, giving you peace of mind.
Commercial Services
Our Services
genetic variations with precise genotyping
Genotyping
Genotyping at Genome X involves analyzing genetic markers to identify variations in your DNA. This precise service provides detailed insights into genetic differences and their implications for health, traits, and diseases. Our advanced genotyping techniques ensure accurate and reliable results, essential for personalized medicine, genetic research, and precision healthcare. By understanding genetic variations, you can make informed decisions about health and wellness.
