Brand
BGI Genomics
BGI Genomics is a leading global provider of integrated solutions in the field of precision medicine. The brand currently serves customers in more than 100 countries worldwide, and its solutions are used in more than 2,300 medical institutions.
Leveraging cutting-edge sequencing and bioinformatics technologies, the company provides its clients with expert and affordable solutions for clinical molecular diagnostics and next-generation sequencing (NGS) services.
To date, more than 150,000 complete human genomes have been sequenced.
Brand mission: to strengthen the prevention and management of genetic diseases, to stimulate and accelerate scientific innovation, and to provide healthcare professionals with cutting-edge diagnostic tools.
Company products
Brand catalog
Molecular genetic diagnostics
PMseq® (Pathogen Metagenomic Sequencing) is a high-throughput metagenomic sequencing platform that enables the...
Molecular genetic diagnostics
NIFTY® Single-Gene Screening (NIFTY® mono) is a non-invasive prenatal screening test designed to detect seriou...
Molecular genetic diagnostics
NIFTY® (Non-Invasive Fetal Trisomy Test) is a modern screening test that safely and accurately identifies the...
Molecular genetic diagnostics
BGI VISTA™ Carrier Screening is a comprehensive solution for prenatal or pre-pregnancy screening for carrier s...
Molecular genetic diagnostics
VISTA™ Chromosome Sequencing is a state-of-the-art NGS platform for the molecular diagnosis of chromosomal abn...
Molecular genetic diagnostics
Newborn Genetic Screening is a highly accurate, next-generation neonatal genetic screening test that detects m...
Molecular genetic diagnostics
BGI VISTA™ PGT-A (Preimplantation Genetic Testing for Aneuploidy) is a highly accurate genetic test performed...
Molecular genetic diagnostics
The BGI XOME™ Targeted Panel is a state-of-the-art solution for the molecular diagnosis of rare inherited dise...
Molecular genetic diagnostics
BGI XOME™ Express is a highly effective solution for the rapid diagnosis of hereditary disorders through whole...
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