Respiratory pathogen panel (RPP) testing checks for a wide range of viruses and bacteria that can cause respiratory infections—like the flu, COVID-19, or RSV—using a single sample. It helps your doctor quickly find the cause of your symptoms and choose the right treatment.

Hereditary cancer genetic testing can help you understand your risk for certain types of cancer, so you and your doctor can take steps to catch it early or even prevent it. It may also help your family members learn about their own health risks.

Genomic testing looks at the unique genetic makeup of your cancer to help your doctor choose treatments that may work best for you. It can also provide insight into how your cancer might behave or respond to certain therapies.

Wound genetic testing analyzes how your body heals and identifies factors that may slow down recovery, such as inflammation or poor tissue response. This helps your care team personalize treatment to promote faster, more effective healing.

UTI (urinary tract infection) testing checks your urine for bacteria or other signs of infection, helping your doctor quickly find the cause of symptoms like burning, urgency, or frequent urination. It ensures you get the right treatment to feel better fast.

Endocrine genetic testing can uncover inherited conditions that affect hormone-producing glands, such as thyroid, adrenal, or pancreas issues, helping guide early diagnosis, treatment, and preventive care. It also offers important health insights for at-risk family members.

Epilepsy genetic testing can help identify the underlying genetic cause of seizures, leading to more accurate diagnoses, tailored treatment plans, and better understanding of potential outcomes. It may also provide important information for family members about their own risk.

Eye genetic testing can detect inherited conditions that affect vision, such as macular degeneration or retinitis pigmentosa, allowing for early intervention and personalized care. It can also help family members understand their own risk and need for monitoring.

Hearing genetic testing can identify inherited causes of hearing loss, helping guide treatment options like hearing aids or cochlear implants and informing decisions about future hearing health. It also helps determine if other family members may be at risk.

Immune genetic testing can reveal inherited conditions that affect your immune system, helping doctors better understand your risk for infections, autoimmune diseases, or certain cancers. It also provides valuable information for family members who may share similar genetic risks.

Liver genetic testing can identify inherited conditions that affect liver function, such as fatty liver disease or cirrhosis, allowing for early detection and personalized treatment. It also helps family members understand their own risk and need for monitoring.

Lung genetic testing can identify inherited risks for lung conditions, including lung cancer or chronic obstructive pulmonary disease (COPD), helping with early detection, prevention, and tailored treatment. It also provides insight into potential risks for family members.

Metabolic genetic testing can uncover inherited conditions that affect how your body processes food and energy, such as diabetes or high cholesterol, allowing for personalized prevention and treatment plans. It also helps identify risks for family members who may share similar genetic traits.

Musculoskeletal genetic testing can identify inherited conditions that affect bones, muscles, and joints, such as osteoporosis or muscular dystrophy, helping guide early diagnosis, treatment, and prevention strategies. It also offers insights into potential risks for family members.

Neurological genetic testing can help identify inherited conditions that affect the brain and nervous system, such as Alzheimer’s, Parkinson’s, or multiple sclerosis, enabling early diagnosis, personalized treatment, and preventive care. It also provides valuable information for family members who may share the same genetic risk.

Renal genetic testing can detect inherited conditions that affect kidney function, such as polycystic kidney disease or kidney cancer, helping with early detection, personalized treatment, and prevention. It also provides insights into the risk for family members who may carry similar genetic traits.

Reproductive genetic testing can identify inherited conditions that may affect fertility or the health of a future pregnancy, such as genetic disorders or carrier status for conditions like cystic fibrosis. It helps guide family planning decisions and provides important information for both partners.

Blood genetic testing can identify inherited conditions that affect your blood, such as sickle cell anemia, hemophilia, or thalassemia, allowing for early diagnosis, personalized treatment, and preventive care. It also provides important information for family members who may share similar genetic risks.

Mutation-specific testing checks for particular gene changes known to drive certain cancers, helping your doctor match you with targeted treatments that are more likely to work. It can also guide clinical trial options and help avoid treatments that may not be effective.

Cardiovascular genetic testing can reveal inherited conditions that affect your heart health, helping you and your doctor take steps to prevent serious problems like heart attacks or sudden cardiac arrest. It can also help family members understand their own risk and need for screening.

Dental genetic testing can identify your risk for conditions like gum disease, tooth decay, or oral cancer, so your dentist can personalize your care and help prevent future problems. It also gives insight into how your genes may affect your response to certain treatments.