To learn more about our genome sequence results:

Review our summarized data results Sequencing Results
Browse our hierarchy of variation calls and genotypes Download Data
Learn more about our sequencing approach Technology Overview

Complete Genomics Data Release

Sample data generated using Complete Genomics’ third-generation human genome sequencing technology are now available. Sequencing of these genomes was conducted at Complete Genomics’ commercial-scale genome center. More information about our sequencing technology may be found here.

These data demonstrate the following features of Complete Genomics' sequencing platform:

  • Produces cost-effective, high-quality, complete human genome data
  • Delivers comprehensive and accurate variation detection
  • Makes accurate calls when compared to orthogonal technologies
  • Yields high quality data with low false-positive, and false discovery rates, suitable for human studies of the genetic basis of disease and cancer

In addition, Complete Genomics has published sequence data and analysis for three human genomes in the journal Science

Summary of Data Results Summary of Data Results in Science
Review the analysis of these genomes as described in the Science publication (Science 327 (5961), 78. [DOI: 10.1126/science.1181498]).

Sequence Data Available for Download Sequence Data Available for Download
Access Complete Genomics sequence data and results.

Legal Disclaimer
These human genomic sequence data are preliminary and may contain errors.

Complete Genomics, Inc. reserves all rights to the genome sequence data and related variations file(s) downloaded here or obtained from Complete Genomics. With access to these data, you agree not to redistribute the genome sequence data or variations file(s) without express written permission. When these genome sequence data (and/or information on sequence variations from a variation file) are used for any publications, you agree to (i) reference the Science publication (R. Drmanac, et. al. Science 327 (5961), 78. [DOI: 10.1126/science.1181498]) and, (ii) provide the version number of the Complete Genomics assembly software with which the data was generated.

Disclaimer of Warranties
COMPLETE GENOMICS, INC. PROVIDES THESE DATA IN GOOD FAITH TO THE RECIPIENT “AS IS.” COMPLETE GENOMICS, INC. MAKES NO REPRESENTATION OR WARRANTY, EXPRESS OR IMPLIED, INCLUDING WITHOUT LIMITATION ANY IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE OR USE, OR ANY OTHER STATUTORY WARRANTY. COMPLETE GENOMICS, INC. ASSUMES NO LEGAL LIABILITY OR RESPONSIBILITY FOR ANY PURPOSE FOR WHICH THE DATA ARE USED.

Any permitted redistribution of the data should carry the Disclaimer of Warranties provided above.

Data file formats and any corresponding API are expected to evolve over time. Complete Genomics cannot guarantee backward compatibility of any file format or API.