Sequence Data and Analysis

Sequence data generated using Complete Genomics' human genome sequencing technology are publicly available for review. Sequencing of these genomes was conducted at Complete Genomics’ commercial-scale genome center.

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 (e.g. SNP microarray data)
• Yields high quality data with low false-positive, and false discovery rates, suitable for human studies of the genetic basis of disease and cancer

Downloads

Complete Genomics provides free public access to whole human genome data sets from the Standard Sequencing Service and the Cancer Sequencing Service.

CGA Tools

Complete Genomics Analysis Tools (CGA™ Tools) is an open source product to provide tools for downstream analysis of genomics data produced by Complete Genomics.

Compatible Third-Party Tools

View a list of the compatible third-party software tools that support Complete Genomics data. Links to the tools are provided.

Data Summary

Review the analysis of sequencing three human genomes as described in the Science publication.

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.