Services


PioneerGenomic is a sub-category of knowledge-based companies that, with the cooperation of a team of the best specialists, has taken steps towards localization and scientific, technological, and commercial advancement and has made unparalleled progress in the fields of bioinformatics, artificial intelligence, biotechnology, and gene therapy. , stem cells, genomics, biotechnology and personalized medicine and cancer. This company was established with the aim of producing knowledge and providing genetic testing services according to the most up-to-date methods in the world (third generation sequencing) and setting up a genetic scientific-research center (R&D)


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WESScreen

Healthy people with no history of genetic disease who decide to get married can do an exoscreen test to ensure that they do not pass on pathogenic mutations with a recessive inheritance pattern to their children. In this test, couples are checked for mutations that cause diseases affecting the quality of life and life-threatening. Exoscreen helps couples in consanguineous or even non-consanguineous marriages to prevent the birth of a baby with genetic defects. Considering the high rate of consanguineous marriages in the Iranian population in the past generations, as well as the higher prevalence of some genetic disorders, unrelated people may also contain the same mutations, which carries the risk of being passed on to the next generation and giving birth to a child with a genetic disorder. By performing an exoscreen test, couples can plan their future options for having a healthy child by knowing their genetic content.


WESCarrier

The purpose of this test is to find pathogenic genetic factors in healthy couples who have a history of genetic diseases in their family members. Sometimes couples who have a history of genetic disease in one or more family members plan to conceive. They are worried that their child might also get a genetic disease. Therefore, by finding possible genetic factors in the genes of the parents, in addition to identifying the cause of the disease in the affected person in the family, this test can prevent their children from contracting a significant part of known genetic diseases by performing tests during and before pregnancy. Also, genetic screening of parents before pregnancy can help reduce the effect of a possible genetic disorder through early diagnosis and treatment.