Cambridge,  MA 
United States
  • Booth: 1021

We Sequence, You discover.

BGI was founded in 1999 to support the Human Genome Project. Since then, BGI has grown into a global genomics company with service laboratories based in the US, Europe, Hong Kong, and mainland China to provide:

  • Next Generation Sequencing Services
  • Mass Spectrometry Services

Our vast scientific experience positions BGI uniquely to support academia and pharmaceutical companies with highly reliable genomic data for basic research and drug development.

We operate all common NGS platforms, as well as our own unique DNBseq™ NGS technology for the best data quality at the lowest cost.

At ASHG 2019, we will feature our full portfolio of NGS services, including True PCR-free WGS and exciting new products:

  • Linked-Read WGS
  • Clinical-Grade WGS

Booth visitors have a chance to win free Long-Read or True PCR-Free WGS services.

Attend out ASHG workshop

To learn more, visit our website or come see us at booth #1021.

 Press Releases

  • Made possible by BGI’s Innovative DNBseq™ NGS technology and Gencove’s ImputeSeq™ bioinformatics, low pass WGS delivers more data for higher statistical power in your GWAS, pharmacogenomics or translational research projects.

    Benefits include:

    • Imputation concordance with deep WGS of up to 99.5%
    • Free of bias from array content
    • Enhanced rare variant discovery  
    • Increased statistical power
    • Unlimited re-analysis of raw data as science progresses

    This new service turns WGS data into highly accurate variant calls across the entire genome and provides ancestry and microbiome profiles, all at the cost of a common genotyping array or less.

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