Complete Genomics has published sequence data and analysis for three human genomes in the journal Science. The data were generated using its third-generation human genome sequencing technology.
These data demonstrate the following features of Complete Genomics' sequencing platform:
- Produces cost-effective, high-quality complete genome data
- Delivers comprehensive and accurate variation detection
- Makes accurate calls when compared to orthogonal technologies
- Yields low false positive and false discovery rates
- Enables high quality data for better understanding the genetic basis of disease
The samples sequenced included cell lines derived from two individuals studied in the HapMap project, a Caucasian male of European descent (NA07022) and a Yoruban female (NA19240). The third sample consisted of lymphoblast DNA from a Personal Genome Project Caucasian male sample, (NA20431). Sequencing of these genomes was conducted at Complete Genomics’ commercial-scale genome center. More information about our sequencing technology can be found here and in the Science publication.
Summary of Data Results
Review the analysis of these genomes as described in the Science publication.
Data Availability
Access Complete Genomics Sequence 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, 5 November 2009 (10.1126/science.1181498)) and (ii) provide the version number of the Complete Genomics assembly software from 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.