Where to get genome sequenced

Choose your plan. Our mission is to usher in the era of personal genomics by providing access to affordable Whole Genome Sequencing and creating technology to protect genomic data privacy. Our offices are located in San Francisco and Boston, two global centers of tech and biotech innovation.

Click here to learn more about us! We ship our sample collection kits to almost every country in the world. Just select your country during checkout. After we receive your sample and decode your DNA, your genomic data and reports will be available through your account on our website. It includes the sequencing of all genes coding regions , regulatory genomic regions, the Y chromosome for males , and mitochondrial DNA. In contrast, other types of genetic tests examine less than 0. It is the best DNA test for health, ancestry as well as the best test for genomic research academia and pharmaceutical companies and public health purposes.

You can learn more about Whole Genome Sequencing and genetics and genomics in general on the websites of the. Centers for Disease Control and Prevention. National Institutes of Health. In contrast to earlier sequencing technologies e. Sanger sequencing , it enables large scale sequencing of many short DNA molecules at the same time. This is much faster than sequencing the full length of the entire genome base-by-base. To determine the order of the short DNA fragments that are output by the sequencing machines, the fragments are computationally mapped to a reference genome and the full-length DNA strands of the newly sequenced genome are reconstructed.

Whole Genome Sequencing identifies all genetic variation in the genome e. For this reason, it is the best DNA test to discover genetic health risks and for diagnosis of genetic conditions. For example, Whole Genome DNA Sequencing can determine if there is an increased risk of developing diseases like hereditary cancers e. It can also uncover carrier status for rare diseases. It enables patients to receive comprehensive genetic counseling and improved medical care that takes the genetic disease into consideration.

Please note that we do not offer diagnostic testing since our DNA test is not prescribed by a physician. Our reporting is intended for educational and informational purposes only.

However, you can bring your Whole Genome Sequencing data to a physician or genetic counselor for various clinical analyses including carrier screening, evaluation of disease risks, and rare disease diagnosis. Through our partnership with YFull available now and FamilyTreeDNA coming in , two leading providers of deep ancestry DNA services, our users will also get access to a large reference population which enables accurate genetic ethnicity estimates ethnic breakdown.

Can you decode that gene and identify mutations? This includes any gene that you might be interested in. This was the cost of sequencing a human genome 20 years ago. What happens if I cancel my subscription? New scientific studies that advance our understanding of human genetics are published almost every day. We charge a subscription fee because we enable our users to benefit from these discoveries.

For example, you will frequently receive multiple new DNA reports that are based on the latest scientific discoveries. Platelets enable clotting. With my Factor V Leiden mutation, I may not need any extra help with that. There are still a lot of questions about how useful genome sequencing is for healthy people.

Lander, himself a pioneer in the sequencing world, hasn't had his own genome sequenced. There are exceptions, he explained — if he had cancer, he'd sequence his tumor, "because there are things you could learn that are directly actionable.

And that's predominantly how sequencing is used in medicine today: in targeted areas like cancer, or to aim to end what researchers call diagnostic odysseys — a long search to turn up the source of a mysterious and serious ailment. Green, my geneticist, is also on the fence about whether healthy people should be sequenced for medical purposes. The findings, he points out, are ambiguous. Mine in particular neither mean I absolutely will have a serious blood clot, nor that I am cleared of worry about other diseases that didn't show up in my results.

And there's always the risk I could overreact. One of my "Variants of Unknown Significance" is a mutation for Lynch syndrome, which predisposes me to certain kinds of cancers, according to my Illumina report. Green disagreed with that finding, telling me he didn't think it was something I should worry about based on his own analysis of the research. But Green's concern is that I could over-worry, and seek unnecessary tests or medical treatment that could do more harm than good.

Or that I'll tell a physician about my Factor V Leiden and he or she will misunderstand the risk and treat me with blood thinners I don't need. I learned I also shouldn't get too complacent about the things my test didn't reveal. That doesn't mean I won't ever get those diseases; it just means this screen didn't turn them up.

The whole genome sequencing isn't guaranteed to find that little area in between there unless you zoom up really close and get next to it. So if I was really concerned about something in particular, it would still be important to get a specific test, not rely on my whole genome sequencing. Green also cautioned that while there are federal laws protecting against employers and health insurers discriminating based on genetic information, there are no such protections in place for life insurance, for example.

Still, he anticipates that within eight to 10 years, it will be routine for healthy people to have their genome sequenced, and for that information to be a regular part of every medical encounter.

Between now and then, costs are expected to continue to come down, reimbursement by insurers is expected to gain more clarity, and more proof is expected about how useful personal genome sequencing can be. As for me, I did find my thumb drive, what Green refers to as my "book of life. When new discoveries are made in genetics, linking certain traits or diseases to different genes, I can delve into my own genome to find out what my personal blueprint tells me.

And with Illumina's svelte iPad app, MyGenome, I can mine my genetic information for even more characteristics about myself than were reported in my clinical analysis. For example, I can search for a variant linked to green eye color, what I learned was located on chromosome I was surprised to find out I don't have it. Perhaps my eyes aren't actually green? On chromosome 11, I discovered I carry a variant that apparently prevents weight gain from high-fat diets.

Note to self: Eat more butter. And I was very happy to learn my results. I can't say I've made any drastic changes to my life as a result of them, but I have started taking walking breaks during longer car rides. And I know that just because I didn't turn up with something — a gene predisposing me to early-onset Alzheimer's disease, for example — that doesn't mean I'm in the clear.

For most of us, genes aren't our destiny. They're a blueprint for how we start out, and then life plays a major role. Well, at least for the next 48 hours. Why the dramatic price drop, which Veritas is taking at a loss? We want to wake them up. This obsessive focus on the number of digits in front of the decimal on the whole genome price tag dates back to December , when scientists gathered at a hotel outside of Washington, DC, to bask in the afterglow of sequencing the first whole human genome.

While somewhat arbitrary at the time, the figure emerged as a mythic technological totem in the world of genetics, sending a generation of DNA geeks chasing after it for the better part of the 21st century. Crack it, the thinking went, and the DNA flood would begin. Surely, everyone would rush to get all of their genetic source code sequenced now? Not so much. That could be because no one has figured out a sexy marketing campaign for whole genomes yet.

Or, more likely, because there are already much cheaper options on the market that will tell you something but not everything! Leadership Initiatives History of Genomics Program. Leadership Initiatives Oral History Collection. Last updated: December 22,