Whole Genome Sequencing
100% DNA Analyzed
Whole genome sequencing involves sequencing the entire DNA of an individual. This means analyzing all 3 billion base pairs of the human genome to enable scientists, researchers and clinicians to decode 100% of an individual's DNA, providing an unprecedented level of knowledge about our genes and our health.
Our commitment
Our advanced sequencing technology and expert analysis enable individuals to access their genetic information with precision and accuracy. With a strong commitment to data privacy and ethical practices, we empower individuals to make informed decisions about their health. Because of its comprehensiveness, our WGS is highly accurate in identifying genetic variants, mutations, and other relevant genetic information. This accuracy makes it extremely useful for diagnosing inherited genetic conditions or assessing the risk of developing them in the future.
The best technology on the market
Traditionally, genetic tests were limited to examining specific genes or regions of the genome. Even to this day, some companies offer analysis of exonic regions of DNA, which correspond to just 5% of the entire genetic makeup. WGS, on the other hand, analyzes 100% of the DNA and thus provides a complete view of an individual's genetic code. It involves reading the order of nucleotides (A, T, C, and G) in an individual's DNA, enabling us to identify variations, mutations, and other genetic markers.
Applications of Whole Genome Sequencing
WGS is at the forefront of the personalized medicine revolution. By understanding an individual's genetic makeup, healthcare providers can tailor treatments and medications to suit their specific genetic profile. This not only improves the effectiveness of treatment but can also reduce the risk of adverse reactions to drugs.
Whole Genome Sequencing Analysis can uncover genetic predispositions to various diseases, including cancer, heart disease, and neurological disorders. Armed with this knowledge, individuals and healthcare professionals can take preventive measures and develop personalized health plans.
WGS is invaluable in advancing scientific research. It allows researchers to identify novel genes associated with diseases, study the genetic basis of complex traits, and gain a deeper understanding of human evolution and migration patterns.
WGS can be used to study genetic diversity in populations of threatened plant and animal species. This information is valuable for biodiversity conservation and natural resource management.