Breaking points:

To identify families of rare diseases Collection of blood samples from the whole family Elimination suppressive mutations, SNP and synonymous mutations The discovery of new mutations >SNP>copy number

Applicable population:

Tumor sufferer: searching for disease genes, to provide tips for the family cancer risk, assist medical doctors to development of therapeutic plans.
People with previous history of cancers or family inherited tumor history, to identify other carriers of the mutant genes in the family through screening, to determine their risk of developing cancers, to achieve early detection, early treatment and reduce morbidity.
Patients suffering from chronic diseases: population with chronic gastroenteritis, history of colitis diseases, to achieve early detection of precancerous lesions through close observation.
Sub-healthy population and healthy people: to provide recommendations for preventive health care.
Genetic screening for prenatal and newborn inherited pathogenic mutation genes.