Genomics. Multi-omnics. And Beyond.

With over 10 years of sequencing experience, a global network of staff, a comprehensive service portfolio, and our own proprietary sequencing technology, we offer our customers a one-stop solution for reliable, cost-efficient and quality sequencing.

Proven DNBSEQTM sequencing technology combines the power of DNA Nanoballs (DNBTM), PCR-free Rolling Circle Replication, Patterned Nano Arrays and cPAS to deliver a new level of data clarity and affordability. The combination of linear amplification and DNB technology reduces the error rate while enhancing the signal, resulting in real advantages. NGS data from DNBSEQTM technology is well documented with over 2000+ peer-reviewed publications and is exclusively available from BGI.

BGI offers multi-omics services to look across genomics, transcriptomics, epigenomics, proteomics and metabolomics, with the flexibility to customize solutions that meet your specific needs.

All projects are supported by a bioinformatics infrastructure that is second to none.

• Experience of processing more than 1,000,000 samples
• Superior SNP/InDel Detection
• 10 working days rapid service available
• gDNA input as low as 50ng

Whole Exome Sequencing

• Experience of processing more than 100,000 samples
• 10 working days rapid service available
• FFPE, low input DNA, saliva samples accepted

Plant & Animal Whole Genome Re-Sequencing

• Even coverage of reads and lower GC content bias
• Experience sequencing over 150 different species
• Higher data utilization

De Novo Sequencing

• Multiple Platforms: DNBSEQ, PB Sequel II, and Oxford Nanopore PromethION
• Hi-C technology: Auxiliary Assembly
• T2T genome assembling accepted
• Assembled more than 250 species so far and published 200 species in top tier journals
• Professional, highly experienced team to help with project evaluation

Metagenomic Sequencing

• Exploring microbial diversity and functional genomics free of pure culture
• Experience of processing 100,000 samples from a variety of environments
• Experience of mGWAS associated with chronic disease

Whole Genome Bisulfite Sequencing

• Even coverage of reads and reliable methylation profiling
• Lower duplication and higher data-use efficiency
• Lower GC content bias

Transcriptome Sequencing

• Multiple Platforms: DNBSEQ, PB Sequel II and Oxford Nanopore
• Multiple protocols to fulfill different sample types
• Experience of processing more than 120,000 samples
• Total RNA input as low as 200pg

Small RNA Sequencing

• Precise quantification by UMI technology
• Experience of processing more than 60,000 samples
• Total RNA input as low as 5ng, exosome RNA also included.

Single Cell Sequencing

• Abondance single cell service experience
• Various sample types handling experience
• Multi-platform's services available
• Both low and high throughput input volume

Premade library sequencing

• 10 working days rapid service available
• Compatible with most library construction kits on the market
• FASTQ files are delivered and suitable for most bioinformatics analysis processes

Proteomics and Metabolomics

• A rich variety of mass spectrometers to satisfy different needs
• Providing gene-expression validating correlation analysis
• More than 10 years of MS experience in the fields of medical, agricultural and microbial research