Sample Preparation and Services
- 150bp (HiSeq X Ten) or 100bp (BGISEQ) paired end sequencing
- Raw data, standard and customized data analysis
- Cloud-based data storage and delivery system
Human whole genome sequencing detects the complete genome sequence at one time and provides the most comprehensive collection of an individual’s genetic variation based on the human reference genome. At BGI we’ve been providing whole human genome sequencing services for over 10 years to support researchers and companies all over the world with their genome sequencing needs, and have seen microarray-based genotyping studies gradually move to whole genome sequencing with the falling costs of sequencing technology.
Whole genome sequencing can be applied to human genetics and evolution studies to detect genome-wide genetic variations, pathogenic and susceptibility genes, and to enable genetic diversity and evolution analysis. It can also be applied to translational research to provide information on cancer and disease-associated mutations and is one of the most important approaches of precision medicine.
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BGI Human Whole Genome Sequencing services are executed with the Illumina HiSeq X Ten, or exclusively with the BGISEQ-500 sequencing system, for great sequencing data at the lowest cost in the industry.
BGISEQ-500 is BGI’s proprietary sequencing platform, developed by our Complete Genomics subsidiary in Silicon Valley.
We are currently offering Human Whole Genome Sequencing from $600 including:
Give our BGISEQ-500 WGS services a try and find out why so many trust their valuable research samples to the world-class sequencing experience of BGI.
Request a No Obligation Quote!
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 Human Whole Genome Sequencing services are executed with the Illumina HiSeq X Ten and BGISEQ-500 sequencing system with the benefit of lower cost and turn-around-time.
We can process your gDNA, Blood, Cell line, Fresh frozen tissue and FFPE samples and
single-cell applications, with the following general requirements:
Regular Samples
Intact genomic DNA ≥ 1μg, Concentration ≥ 12.5ng/ μl
15 μl
Low Input Samples
Intact genomic DNA ≥ 200ng, 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.
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
CNV calling and annotation
SV calling and annotation
Cancer Somatic Mutation analysis
Population genetics analysis
Complex disease 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.
