Advancing Human Genome Sequencing

By enabling cost-effective comparisons of genomes from thousands of individuals, Complete Genomics will transform the way disease is studied, diagnosed and treated, ushering in a new era in genomic medicine. These advances will in turn lead to more accurate molecular diagnostics for complex diseases such as cancer, improved drug therapies and personalized medical treatment.

New Service-based Approach

Through its service model, Complete Genomics will provide customers with access to high-quality, low-cost human DNA sequencing data with no capital expenditure. Customers no longer need to dedicate resources to preparing and operating sequencing instruments nor invest in the considerable computing resources required to manage and analyze the substantial data generated. Customers are free to focus on their areas of expertise.

Large-Scale Sequencing

Complete Genomics’ genome and data centers are being custom built to handle the massive sequencing throughput and data volume generated by large-scale comparative genomic analyses. By servicing hundreds of customers through a central genome center, Complete Genomics can offer its customers superior human sequencing, data management and analytic capabilities.

Human Focus

As Complete Genomics focuses solely on human DNA sequencing services, its technologists are highly specialized experts in the field. Sample preparation processes are designed for the human genome and software is optimized for assembling and analyzing human DNA.

DNA Sequencing Applications

Complete Genomics’ human DNA sequencing services will be tailored to meet customers’ needs. The company’s efficient genomic data pipeline and powerful data management systems, combined with project management and human sequencing expertise, will allow large-scale human genome sequencing projects to be completed quickly with industry-leading quality.

Complete Genomics’ technology, provided as a service, opens the door to exciting possibilities in key areas of human genome resequencing including:

• Complete human genome resequencing
• Genome subsetting, such as candidate regions or exon sequencing
• Structural variation and copy number variation (CNV) analysis
• Genomic rearrangements and allelic imbalances

Advantages of our comprehensive human genomic services include:

• Dedicated and proven human DNA sequencing experience
• Unprecedented scale through our commercial genome center
• Affordable, high quality sequencing results
• Superior project management

By enabling cost-effective comparisons of genomes from thousands of individuals, Complete Genomics will unlock a new era in genomic medicine. This will enable researchers to transform the way disease is studied, diagnosed and treated in turn leading to more accurate molecular diagnostics for cancer and other diseases, improved drug therapies and personalized medical treatments.

For more information on Complete Genomics’ services, please contact info@completegenomics.com.

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