Clinical Genomics

HorizonDx™

Comprehensive Carrier Screening

A comprehensive genetic test designed to determine an individual’s carrier status for a wide range of inherited conditions.

Unlocking Genetic Insights

InsightDx™ uses Whole Exome Sequencing (WES) to analyze all protein-coding regions of your genes – the part most often linked to genetic disorders. By focusing on the 20,000+ genes that drive about 85% of known disease-causing variants, it helps doctors pinpoint the cause of unexplained symptoms faster and more accurately. Whether it’s diagnosing complex conditions, uncovering hidden mutations, or guiding treatment decisions, WES provides a powerful, efficient way to bring clarity to patients and families facing genetic uncertainty.

Download Brochure

Clarity for Confident Family Planning

Carrier screening provides couples with crucial insights before pregnancy or fertility treatments, helping them understand potential risks and make informed reproductive choices. This foresight allows families to plan with confidence, explore alternative options if needed, and take proactive steps toward a healthy future.

Early Preparation, Better Outcomes

By identifying carrier status early, families gain the knowledge and time to consider their options with clarity and peace of mind. This awareness helps them prepare emotionally, explore medical guidance, and make informed decisions before complications arise—transforming uncertainty into proactive steps for a healthier future.

Prepare emotionally, medically, and financially for potential challenges
Reduce uncertainty by identifying risks not revealed by family history
Support timely interventions and improved health outcomes for newborns

Genomics for Families and Newborns

Comprehensive carrier screening, newborn health insights, and disease risk prediction to guide early intervention. Enable personalised care, informed family planning, and lifelong health management with advanced genomic testing.

Carrier Screening Facilitates Informed Decision-making And Early Preparation

Each of us carries at least one genetic condition. Most carriers are healthy and have no family history, yet they face the risk of transmitting a genetic condition to their offspring. Genetic carrier screening is a test that determines whether you possess a gene with a modification, or variant, that could influence your child's health. When conducted before conception, genetic carrier screening offers valuable information, allowing individuals to consider alternative reproductive choices. During pregnancy, carrier screening assists couples in making informed decisions about prenatal or newborn diagnostic testing, and if needed, aids in emotionally, medically, and financially preparing for a baby with a genetic condition.

Comprehensive and Reliable Screening

Our advanced next-generation sequencing technology analyzes 100% of the exome or genome, delivering the most thorough evaluation of potential genetic conditions in a single test—no need for multiple screenings.

Trusted by Medical Professionals

HorizonDx™ is backed by clinicians who rely on its accuracy and effectiveness, ensuring you receive results you can trust when making important family planning decisions.

Expert Guidance at Every Step

Board-certified genetic counselors provide complimentary sessions before and after testing, offering clarity, support, and reassurance as you navigate your results.

Convenient and Accessible Testing

Choose the method that works best for you: mobile phlebotomy services for at-home blood draws or a simple saliva kit as a comfortable, needle-free option.