For many applications, Whole Exome Sequencing is gaining popularity as a viable and cost-effective alternative for Whole Genome Sequencing. BGI has performed professional sequencing services for many years at multiple locations globally, to support biomedical research and to benefit small and large-scale clinical trials and other projects in pharmaceutical drug development.
Besides raw sequencing data output, BGI offers standard and custom bioinformatics services to suit your specific research needs.
BGI Whole Exome Sequencing services are executed with the Illumina sequencing system, or exclusively with our DNBseq™ NGS platform , for great sequencing data at the lowest cost in the industry.
DNBseq™ is a high-throughput sequencing platform developed by a subsidiary of BGI, Complete Genomics, in Silicon Valley. This system is powered by combinatorial Probe-Anchor Synthesis (cPAS), linear isothermal Rolling-Circle Replication and DNA Nanoballs (DNBTM) technology, followed by high-resolution digital imaging.
Ask your BGI representative about our current introductory pricing for Whole Exome Sequencing with the BGI’s own DNBseq™ sequencing system.
We care for your samples from the start through to the result reporting. Highly experienced laboratory professionals follow strict quality procedures to ensure the integrity of your results.
Send us a no obligation request for quote and our dedicated sales team will reply to you within 24 hours.
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BGI Whole Exome Sequencing services are executed on Illumina platforms or the DNBseq™ sequencing system with the benefit of lower cost and turnaround time.
We can process your gDNA, Blood, Cell line, Fresh frozen tissue, FFPE samples and single cell applications from human and rodents, with the following general requirements:
Regular Samples
Intact genomic DNA ≥ 1µg, Concentration ≥ 12.5 ng/ µl
15 μl
Low Input Samples
Genomic DNA ≥ 200 ng, Concentration ≥ 2.5 ng/ µl
15 μl
In addition to raw data output, BGI offers a range of standard and customized bioinformatics pipelines for your whole genome sequencing project. Reports and output data files are delivered in industry standard file formats: BAM,.xls, and .png
Filtering
Alignment
SNP calling and annotation
SNP validation and comparison
SNP functionality and conservation prediction
SNP statistics per functional element
InDel calling and annotation
InDel validation and comparison
InDel statistics per functional element
Cancer Somatic Mutation analysis
Mendelian disease analysis
De novo mutation analysis for family samples
Further customization of Bioinformatics analysis to suit your unique project is available: Please contact your BGI technical representative
We care for your samples from the start through to the result reporting. Highly experienced laboratory professionals follow strict quality procedures to ensure the integrity of your results.
