Exome Sequencing
Our Exome Sequencing service is a highly popular and cost effective alternative for WGS for both basic research and clinical purposes. Contact us today with any questions or for a no obligation quote.
Exome Sequencing Introduction
Whole Exome Sequencing is a popular and cost-effective alternative for Whole Genome Sequencing, especially for clinical research applications. BGI provides professional exome sequencing services for clinical resarch purposes at multiple locations globally to support biomedical research, 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. Please contact us with your requirements and our experts will be happy to help.
25 years of exome sequencing experience.
Guaranteed data quality at competitive pricing enabled by proprietary technology.
Rapid turn around times and expert project support.
Whole Exome Sequencing Service Overview
Sample Requirements
Regular Samples
- Intact genomic DNA: ≥ 500 ng
- Concentration: ≥ 12.5 ng/µL
- Volume: 15 µL
Low Input Samples
- Genomic DNA: ≥ 200 ng
- Concentration: ≥ 2.5 ng/µL
- Volume: 15 µL
Sequencing Standards
• 100bp and 150bp paired-end sequencing options available
• Guaranteed ≥ 85% of bases with quality score of ≥Q30
• Standard sequencing coverage ≥100X; ≥200X is recommended for cancer samples
Key Service Details
• Typical 18 working days from sample QC acceptance to data availability.
• Expedited services are available, contact your local BGI specialist for details
• Reports and output data files are delivered in industry standard file formats: BAM, .xls, .png and FASTQ data.
Unique DNBSEQ™ Sequencing Technology
BGI Genomics' Human Whole Genome Sequencing services are typically executed with proprietary DNBSEQ™ sequencing technology platforms, for great sequencing data at some of the lowest costs in the industry. DNBSEQ™ can offer advantages in terms of lower amplification error rates and much lower duplication rates in WGS/WES applications. In addition, studies have shown the lower index hopping rate in DNBSEQ™ platforms.
Contact us with any general enquiries or questions for our sequencing experts, we are here to help.
Access Further Sequencing Resources
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. Access more sequencing resources below for full access to our range of educational resources and sample guides.
