personal genome sequencing assesses the status of all of your genes at one time, just as if the “human genome project” were conducted specifically on you.
an analysis of your entire genome would not only assess genes that are implicated in disease, but could also reveal information about your physical traits, your behavior, and even your ancestry. the application of genomic information could enhance our ability to make informed and appropriate decisions regarding health care, including, for example, the treatment of specific diseases or predispositions and the choice of drugs and drug dosage.
ugenomics can simultaneously examine the four "killers" of the human health —cancer, cardio-cerebral-vascular disease, birth defect/genetic disease and adverse drug reaction. before the attack of these major diseases, personal genetic test can analyze the molecular genetic pathology to forecast and prevent tumor.
health risk:personal genome test can evaluate cancer, heart and cerebral vessel diseases , nervous system diseases , metabolism and internal secretion disorder and monogenic disease, helping us realize early prevention and make scientific and healthy life management solution.
personalized medicine: the polymorphism of genome is one main factor influencing metabolic capacity, therapeutic effect and toxic and side effect. the personal genome test can help patients receive professional targeted therapeutic options by integrating personal genetic information.
personal feature:gene is the decisive factor influencing individual features such as appearance, figure and alcohol tolerance. personal genome test can provide professional personal feature genetic test, which is helpful for knowing personal feature and potentials.
advanced:the illumina high-throughput sequencing system and bioinformatics analysis platform are adopted.
comprehensive:we offer a comprehensive personal genome gene report, including health risk, personalized medicine and personal feature.
professional:the interpretation of the test is based upon our powerful database including both the authoritative databases and the latest clinical research results.
personalized:we depending your unique genetic testing report to provide you personal health management recommendations.
people commonly use the terms "mutant" and mutation" to describe something undesirable or broken. but mutation is not always bad. most dna changes fall in the large areas of the genome that sit between genes, and usually they have no effect. when variations occur within genes, there is more often a consequence, but even then mutation only rarely causes death or disease. mutation also generates new variations that can give an individual a survival advantage. and most often, mutation gives rise to variations that are neither good nor bad, just different.
because genetic testing tells you information about your dna, which is shared with other family members, sometimes a genetic test result may have implications for blood relatives of the person who had testing.
genetic test results can be hard to understand, however specialists like geneticists and genetic counselors can help explain what results might mean to you and your family.
genomics produces huge volumes of data; each human genome has 20,000-25,000 genes comprised of 3 million base pairs. we need enough time to interpret the data.