BGI VISTA™ Carrier Screening
Most people do not know they are a carrier for an inherited genetic disease until they have a child with the disease. The Vista™ Carrier Screening detects 15,000 mutations across 547 genes, for 626 autosomal-recessive and X-linked genetic disorders.
BGI VISTA™ Carrier Screening can be ordered before or during pregnancy and is ideally suited for couples who want to learn about their genetic status, so that they can make more informed reproductive decisions.
BGI VISTA™ Carrier Screening covers most common disease such as:
BGI VISTA PGS/PGD
Preimplantation genetic screening (PGS) evaluates embryos for extra or missing chromosomes. PGS is an option for any in vitro fertilization (IVF) patient.
BGI VISTA™ PGS is used in conjunction with an IVF cycle. Embryos remain on-site at the patient’s IVF center. Cells are removed from an embryo and sent to BGI for genetic analysis.
BGI VISTA™ PGS can improve the chance of a successful pregnancy while reducing the chance of miscarriage or of havinga child with a chromosome condition.