Joint Care DNA™
Joints need collagen to help maintain the tendons and ligaments that support your body.Joint Care DNA™ tests the genes that may influence your collagen quality and overall joint health while providing you with a recommendation to help you support your overall joint health. The test examines 9 Autosomal markers (SNPs) that impact your collagen and determines if your body has a genetic variant. Third-party research identifies variants in these 9 SNPs that may influence the quality of collagen produced by the body which may influence your joint health
PathwayFit® is a genetic nutrition and exercise profile that tells you how you may react to specific types of food and exercise and provides insights into how your body may process sugars, fats, nutrients, and vitamins. Pathway provides a personalized report that has powerful information and recommendations – all aimed at helping you optimize your health.
DNA Healthy Weight
Eliminate the guesswork for getting to and maintaining a healthy weight. HomeDNA™ DNA Healthy Weight is a scientifically-based weight-management test and program that identifies your unique genetic makeup and provides diet and exercise strategies specifically to your genotype. Just take the simple at-home DNA test and within a few weeks, you will receive a personalized nutrition and fitness recommendations that work best for your body. Get ready to take control of your health.
Cytogenetic Tests for Chromosomal Abnormalities
Protected: Fitness & Diet Genetic Test
Due to our genetic makeup, we are all different in many ways. There are the physicial differences such as eye and hair color, but then there are the differences inside us such as how we metabolize nutrients, the way we deal with toxins etc. We all interact with the
environment in our own unique way. The fitness & diet genetic test helps identify an individual’s genetic predisposition for sporting or fitness profile, idea diet, and personal nutrition needs based entirely on genes.
Whole Genome Sequencing
Human whole genome has approximately 3 billion base pairs of nucleotides. The first human whole genome sequencing (hWGS) was completed and published in 2001. Since then, hWGS is widely studied in the filed of biomedical science, anthropology, forensics and many more. Individual variations, such as single nucleotide polymorphism (SNP), copy number variation (CNV) and structural variations (SV), can be identified by whole genome re-sequencing.
Retinal Degeneration Panel
Mutations in more than 60 genes are known to cause nonsyndromic retinitis pigmentosa. Mutations in any of the genes responsible for retinitis pigmentosa lead to a gradual loss of rods and cones in the retina. The progressive degeneration of these cells causes the characteristic pattern of vision loss that occurs in people with retinitis pigmentosa. Rods typically break down before cones, which is why night vision impairment is usually the first sign of the disorder. Daytime vision is disrupted later, as both rods and cones are lost. Retinitis pigmentosa often has an autosomal dominant, or autosomal recessive , or X-linked pattern.
InSure® FIT™ is a CLIA waived test that is available for Physician Office Lab (POL) testing. To help improve
colorectal cancer screening compliance, InSure®FIT™ screening test offers high sensitivity and ease of use. It is a highly patient-friendly water-Based collection method. It’s patented brush sampling replaces unpleasant fecal collection or smearing and there are no dietary or medication restrictions. InSure® FIT™ has 87% sensitivity for colorectal cancer & 98% specificity. The test has a 66% increase in patient compliance versus a guaiac-based fecal occult blood test (gFOBT) based on a recent study1.
Metals Hair Test
Heavy metals toxicity caused by increasing levels of pollution and use of chemicals in industry is a growing threat to our health and development of our children. High levels of toxic metals deposited in body tissues and subsequently in the brain, may cause significant developmental and neurological damage. A Metals Hair Test is ideal for checking current exposure to toxic metals. Hair provides important information that can assist the practitioner with an early diagnosis of physiological disorders associated with aberrations in essential and toxic element metabolism.
GynPlus is a next generation sequencing panel that simultaneously analyzes 9 high-risk ovarian and uterine cancer susceptibility genes Genes on this panel include BRCA1, BRCA2, EPCAM, MLH1, MSH2, MSH6, PMS2, PTEN, and TP53. These nine genes are associated with four hereditary cancer syndromes hereditary breast and ovarian cancer (HBOC), Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome, all of which have published management guidelines. Identification of a mutation in one of these genes can help estimate cancer risk and guide treatment, screening, and/or prevention decisions for the patient.
Urine Hormones Metabolites
Test assesses both parent hormones and their corresponding metabolites, it reveals how the body is breaking down key hormones like estrogens, progestogens, androgens, cortisol and melatonin. This testing gives insight into whether we are fully detoxifying our hormones, which is important because some hormones can be carcinogenic if they don’t break down properly – leaving us more at
risk for a variety of diseases, like cancer.
Testing neurotransmitters in patients with psychological conditions can help target specific imbalances – getting to the root of persistent issues such as adrenal dysfunction, mood disorders, lack of ambition and lack of appetite. Neurotransmitter testing gives practitioners a diagnostic edge over the traditional psychological inventory. It offers the advantage of zeroing in on which therapies are best suited for an individual patient. Combining neurotransmitter testing with other hormone testing gives practitioners an even deeper insight into a patient’s Individual neurochemistry.