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.
BGI VISTA™ Chromosome Sequencing is especially suitable for:
12 working days
Abortion Tissue, Core Blood (Gestation week >12 weeks), Peripheral Blood, DNA and Amniotic Fluid.
Low coverage WGS
BGI VISTA™ Chromosome Sequencing-1M: deletions or duplications >1Mb
BGI VISTA™ Chromosome Sequencing-100K: deletions or duplications >100Kb
Ordering BGI VISTA™ Chromosome Sequencing is easy.
Physician orders test
Sample shipped to BGI and analyzed
Results sent to physician