Secondary Interpretation

Some individuals may wish to seek additional information about genetic disease associations and risks.

The following companies will accept your genome sequence data and provide further analysis and interpretation options downstream of our IGS services. Each company provides different services and establishes their own fees. For more information on these options, contact the specific company directly.

		23andMe 2606 Bayshore Parkway Mountain View, CA 94043 Phone: 650.938.6300 www.23andMe.com 23andMe is dedicated to helping individuals understand their own genetic information using recent advances in DNA analysis technologies and web-based interactive tools. 23andMe enables individuals to gain deeper insights into their personal health, ancestry, and inherited traits as well as giving them the opportunity to advance genetic research through participation in 23andMe’s research studies.



		deCODEMe Contact: Edward Farmer edward.farmer@decode.is Phone: +44 7796 010107 deCODE genetics is a global leader in the discovery of genetic risk factors for common diseases and in the development of DNA-based reference laboratory tests and consumer genome analysis. deCODEme, the world's first personal genome scan, enables individuals to get a detailed and scientifically validated look at their own genome and what it can tell them about their susceptibility to a range of common diseases and other traits.



		Knome 101 Main Street, 16th Floor Cambridge, MA 02142 info@knome.com Phone: 617.528.1672 The KnomeEssential and KnomeSentinel offerings being made available through Illumina's Personal Genome Sequencing service are based on Knome's first-of-its-kind genome browsing software application (KnomeXplorer). These tools allow individuals to navigate through their own DNA and to remain current on the latest research as soon as it becomes available.



		Navigenics Contact: Brenna Sweeney bsweeney@navigenics.com 1001 E Hillsdale Blvd, Suite 550 Foster City, CA 94404 Phone: 650.585.7523 http://www.navigenics.com/ Navigenics provides personalized genetic testing focused exclusively on your health. The company reveals your genetic risk for a variety of health conditions, including breast cancer, diabetes and heart attack and gives you the tools and support to help you work with your doctor to live healthier and take powerful steps toward prevention.



		NCGR Contact: Callum J. Bell Ph.D. cjb@ncgr.org 2935 Rodeo Park Drive East Santa Fe, New Mexico 87505 Phone: 505.995.4428 http://www.ncgr.org/ NCGR is a non-profit research institute dedicated to improving human health and nutrition by genome sequencing and analysis. With its award-winning Alpheus software system, NCGR can provide a detailed analysis of your personal genome sequence. Utilizing its experience in genome sequencing, NCGR compares your individual genome sequence to the reference human genome to identify points at which your genome differs. NCGR explains what these differences are likely to mean, along with an interpretation of the technical stuff. NCGR strives to work with families and their genome information to create a better understanding of the genomic basis of health, attributes, and disease.



		Pathway Genomics Contact: Jim Woodman 4045 Sorrento Valley Blvd. San Diego, CA 92121 Phone: 858.450.6600 www.Pathway.com Pathway Genomics will walk you through your personal genome sequence to uncover your genetic health risks, discover your ancestral path, determine your carrier status, identify adverse drug responses, and explore personal traits unique to you. As your partner, Pathway’s genetic counselors are available to help you understand this in-depth view of your genes, so that you can find ways to maintain your health and wellness. Pathway is located in San Diego, CA and is the only consumer genetic testing company to receive state and federal government certification for processing human DNA laboratory tests.



		Promethease http://www.snpedia.com/index.php/Promethease Promethease is a data analysis tool that allows you to build a report based on SNPedia and a file of genotypes. This tool can be used by physicians and their patients to learn more about their DNA through their sequencing or genotyping data. It can also pool the data from multiple testing services. The program runs for approximately three hours. If you make an optional $2 payment (per run of Promethease) via Amazon.com you can increase the speed of the run.

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SUBMIT

Illumina

Please note:
Individual Genome Sequencing will be performed in Illumina's CLIA (Clinical Laboratory Improvements Amendment)-certified and CAP (College of American Pathologists)-accredited Clinical Services Laboratory's, under a valid and unexpired California Clinical Laboratory License. The Individual Genome Sequence information is generated by licensed personnel using an analytically validated process. Consistent with Lab Developed Tests, it has not been cleared or approved by the U.S. Food and Drug Administration.

This genome sequence information can be analyzed to potentially aid your doctor in the evaluation of a broad range of health conditions or physiological traits. You will not receive medical results, or a diagnosis, or a recommendation for treatment from Illumina. Any results arising from the analysis of your genome sequence information that might be deemed medically actionable should be confirmed using alternative testing. If you have any questions or concerns about what you learn through your genome sequence information, you should contact your doctor or a genetic counselor.

Currently Illumina does not accept orders for individual genome sequencing services from the following states: Florida, New York, and Rhode Island.