VISTATM 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 11,000 mutations across 161 genes, for more than 169 genetic disorder.
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.
Option 1: BGI VISTA™ Carrier Screening Targeted Panel 2.0 (screening of 155 conditions)
Option 2: BGI VISTA™ Carrier Screening mini Panel (screening of 11 conditions)
BGI VISTA™ Carrier Screening covers most common disease such as:
Why Choose BGI VISTA™ Carrier Screening?
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 having a child with a chromosome condition.
Who should consider BGI VISTA™ PGS?
Any Individual or couple undergoing IVF, especially those with the following indications:
Why Choose BGI VISTA™ PGS?
VISTATM Chromosome Sequencing
BGI VISTA™ Chromosome Sequencing uses NGS based low coverage whole genome sequencing (WGS) to help detect chromosome abnormalities before or during pregnancy. Testing can be performed on a variety of different sample types.
Option 1: BGI VISTA™ Chromosome Sequencing-5M: deletions or duplications >5Mb
Option 2: BGI VISTA™ Chromosome Sequencing-5M: deletions or duplications >100Kb