The sequence of drug metabolic genes in each human body determines individual's drug metabolism and tolerable doses. Individualized medication that only takes age, gender and health status into account is far from enough. It must also consider individual difference in genes, which in turn it can ensure the safe use of drugs.

The use of DNA testing technologies which can crack the secrets of DNA related drug responses, reveals patient's adverse effects on different drugs and provides scientific and precise guidance to clinical medicine. With reference of DNA testing results, doctors can make suitable medication plan containing drug selection, dose control, and drug combination, etc., for each patient. Ultimately it will improve drug efficacy, reduce side effects, and lower medical expenses.

Whole genome sequencing has a wide coverage. It can detect all the genetic information in the genome with the accuracy rate as high as 99.99%.

Thousands of diseases, individual traits, behaviors, and abilities in human are genetically determined or related. Whole genome sequencing reveals the mysteries of birth, aging, sickness, and death, giving mankind the opportunity to fundamentally recognize the onset of diseases. It realizes early prevention and correct treatment of disease. GPBio provides you with genome-wide sequencing, allowing you to immediately get hold of your entire life blueprint.

Diet management in traditional Chinese medicine helps maintain the health of the body through slight adjustments of nutrition combination. However, if differences in nutrition related genes between people are not reasonably considered, the effect of diet management will be weakened. Through the detection of genes related to metabolic diseases, blind care can be turned into a purposeful health management.

From diabetes to osteoporosis, or from female natural menopause age to vitamin absorption and metabolism capacity, through genetic testing, not only prediction of illness risks is available, better understanding of the possible causes of illness is feasible as well.

Genetic disease detection in both husband and wife expecting a baby can effectively reduce the occurrence of birth defects in children, and also effectively reduce or even avoid the burden on the families.

Through neonatal screening of genetic diseases, birth defects from genetic reasons can receive early diagnosis and treatment before clinical manifestations or mild symptom is observed,

thus effectively prevent the body tissues and organs from irreversible damages, which greatly reduce children mortality with mental retardation, physical disability, and other serious diseases.

The rate of allergic diseases has shown a global growth. According to epidemiological surveys, allergic diseases increased by at least 3 times in the past 30 years, covering more than 22% of the world's population. It has become the world's sixth largest disease class. As a result, allergy and anti-allergy, is an inevitable challenge confronting modern people.