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What is genetic testing?
Every individual has a different genetic makeup and hence different set of health issues. By understanding and testing DNA we are able to:
- Confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder
- Identify the root cause of existing health problems and also provide targeted solutions.
- Make necessary lifestyle changes, whether it is altering your food habits or knowing which foods you should eat more (food that your body lacks) or which foods you must control and if possible avoid (that your body is allergic, intolerant and sensitive to).
Whole Body Senquencing : 30 million base pairs are scanned.
Whole genome sequencing is the mapping out of a person’s unique DNA. Your genome is the unique blueprint for your body. Sometimes, because of new or inherited genetic mutations, your genes can cause a disease or increase your risk for disease. By sequencing your genome, health professionals can look at the unique variations found in your genes.
It is most often used in medical research and is beginning to be used more in clinical practice. For example, a doctor or genetic counselor could use whole genome sequencing to see if a patient has a genetic disorder or is at risk for a disease.
- Family Diseases
- Nutritional and Metabolic Diseases
- Congenital, Hereditary, and Neonatal Diseases
- Stomatognathic Diseases
- Otorhinolaryngologic Diseases
- Eye Diseases
- Skin and Connective Tissue Diseases
- Cardiovascular Diseases
- Hemic and Lymphatic Diseases
- Musculoskeletal Diseases
- Digestive System Diseases
- Male Urogenital Diseases and Abnormalities
- Endocrine System Diseases
- Respiratory Tract Diseases
- Nervous System Diseases
- Immune System Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Neoplasms


NGS and Genetic testing
- Next generation sequencing (NGS) has been an invaluable tool to put genomic sequencing into clinical practice
- The incorporation of clinically relevant target sequences into NGS‐based gene panel tests has generated practical diagnostic tools that enable individualized patient care
- The speed, throughput, and accuracy of NGS has revolutionized genetic analysis and enabled new applications in genomic and clinical research, reproductive health, and environmental, agricultural, and forensic science

