Whole Genome and
Whole Exome Sequencing
Comprehensive genetic profiles can now be unlocked using the latest Next Generation Sequencing technology. It identifies variances in DNA and screens for a predisposition toward medical issues, the cause of medical conditions and can identify a health risk. It’s both a fast and reliable way to diagnose conditions by unlocking the entire protein-coding regions of the genome.
The genome is the entire DNA content that is present within one cell and is approximately 6 billion letters long, repeating sequences A,G,T, C. They teach all your cells how to operate with the genetic code, acting like an instruction manual for how the body functions. As knowledge continues to evolve in genetics, Whole Exome Sequencing (WES) and Whole Genome Sequencing (WGS) are being introduced to practitioners to identify a patient’s genetic code for better care or to identify more precise treatment.
Pharmacogenomics (PGx)
Pharmacogenomics (PGx) is the study of how genetic variations influence the way an individual responds to medications. Our testing identifies variations in a number of genes that influences responses to medications. PGx is now enabling doctors to test for specific genetic changes to predict whether a patient may have a normal response, a poor response, or a higher risk of side effects before prescribing a specific medication.
We concentrate on the genes encoding the metabolizing enzymes (i.e. CYP450 enzymes) which are found mainly in the liver and the gut wall. These genetic variations predict the level of enzyme activity which in turn results in increased or decreased plasma concentrations and drug exposure.
Increased plasma concentrations, due to reduced enzyme activity, can lead to adverse effects. Reduced plasma concentrations, due to increased enzyme activity, can lead to poor therapeutic response.
We offer Multiple Category Medication testing including pain, oncology, gastrointestinal, cardiovascular and psychotropic medications. Alternatively, a Psychotropic Medication Test is available as a single category.
Comprehensive Health
Nutrigenomics is the study of how foods interact with your genes and explains the individual genetic differences that can affect the requirements of vitamins, minerals, and compounds in the foods we eat. Everyone absorbs, metabolizes, and transports chemicals differently based on their genetic makeup; nutrigenomics unlocks this personal blueprint.
Our reports cover digestion, energy, hormones, stress & cognitive performance, Inflammation 7 longevity, athletic performance, DNA protection & repair, detoxification.
Our DNA Comprehensive Health Reports are powerful, personalized, and easy to interpret. We analyze thousands of complex gene combinations, taking weighted and cumulative value into account to provide the most accurate and personalized action plan possible. Our reports cover over 92 clinically relevant genes with over 900 research studies.
