Complete Genomics’ Innovative Service

Unlike other sequencing companies that primarily sell DNA sequencing instruments and reagents that produce raw sequenced data, Complete Genomics offers an end-to-end, outsourced solution that enables our customers to offload to us the complex processes of sample preparation, sequencing, computing and data storage and management.

Our Complete Genomics Analysis Service, CGA™ Service, provides academic and biopharmaceutical researchers with complete human genomic data and analysis at an unprecedented quality, cost and scale without requiring them to invest in in-house sequencing instruments, high-performance computing resources and specialized personnel.

Process

Our Complete Genomics Analysis Service, CGA Service, is a simple, cost-effective service in which customers send DNA samples and receive high quality, research-ready data for accelerated scientific discovery.   Our genome sequencing center combines:

  • High-throughput sample preparation facility
  • Collection of our proprietary high-throughput sequencing instruments
  • Large scale data center

Customers ship us their DNA samples via common carrier services such as Federal Express and United Parcel Service. We then sequence and analyze these samples and provide our customers with the fully assembled sequence data and variant reports including annotated lists of sequence variants detected in each genome.

This research-ready data allows researchers to rapidly identify genes and pathways expediting the path to biological results., and our convenient service model enables customers to focus exclusively on their single highest priority, discovery.

Service Advantages

Advantages of our comprehensive human genome sequencing services include:

  • Faster Time to Results: No need to invest significant additional resources to conduct samples preparation, run instruments and process the raw data. Receive research-ready genomic data with access to integrated, advanced informatics and data management services.
  • Quality:  By combining our proprietary sequencing technology with specialized algorithms and computational approaches designed to address the unique characteristics of human genomes, customers receive high quality sequence data. Learn more about Complete Genomics data management and analysis capabilities.
  • Scale: Complete Genomics’ sequencing and data center are custom built to handle the massive sequencing throughput and data volume generated by its high-throughput genome sequencers.  And because our technology resides in our centralized facilities, we can quickly and easily implement enhancements and provide their benefits to our entire customer base.

Complete Genomics is dedicated to providing on-demand, affordable, high quality sequence data from thousands of samples.  Our service is unlocking a new era in disease research and is transforming the way diseases are studied by providing high-quality complete genome sequence data to all researchers.

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

Additional Materials

To Get the Whole Picture, Sequence the Whole Genome

Next-generation DNA sequencing has recently empowered scientists to identify genetic variations associated with human disease at higher resolution and greater sensitivity than previously possible. Two approaches are commonly employed -- exome sequencing and whole genome sequencing. Exome sequencing targets protein-coding regions comprising approximately 1% of the human genome, while whole genome sequencing uses an unbiased approach to investigate the majority of the human genome, including a comprehensive survey of coding and non-coding regions.

>> read more

Complete Genome Sequencing of a Nuclear Family Reveals Candidate Genes for Rare Genetic Diseases

Ever since the human genome was first sequenced, scientists have been inspired by possibilities of using genomic...

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