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Complete Genomics, a BGI company, has developed an advanced platform with industry leading accuracy and sensitive detection of a wide range of variants across the genome. Our innovative and experienced NGS scientists have improved the sequencing workflow and we can now provide whole exome sequencing service in addition to whole genome sequencing on the Complete Genomics platform. More applications are in development.


Promotion Details:
Human Exome Sequencing (100X) for $599/sample new
100X deep exome sequencing enables researchers to get better coverage and discover more variants
Turnaround time: 35 working days for up to 280 samples
Analysis included: exome assembly, SNP and indel calling, filtering, and annotation
SNP validation of 140 loci will be provided upon request at no additional cost to ensure the accuracy of your results
*Additional quantity discount available for large projects!

Advantages of the Complete Genomics Platform:
Industry-leading accuracy enabled by Complete Genomics’ novel sequencing chemistry, combined with advanced algorithms for mapping and assembly.
Advanced analysis pipeline addressing cancer study designs and challenges.
Proven platform and expertise: Over 15,000 genomes have been sequenced and analyzed on this platform with publications in top tier journals such as Nature and Science.
Continuous innovation: Recent improvements in the chemistry have shortened turn-around time and more applications are in development.

Contact us to learn more!