Your genomes are sequenced in one of our selected third-party partner labs in either Germany, Denmark, New Jersey (USA) or Hong Kong. Before selecting the best partners to sequence your DNA we ran pilots and reviewed more than 15 genetic labs. All of our partner labs are certified, and we have worked with them to implement special quality workflows, going beyond the normal regulatory measures. We have now setup our own laboratory in L’Aquila, Italy, [ in the university district, near the GSSI PhD school]. Looking forward, more and more samples will be analyzed internally.
Yes. We do ship globally. Free shipping.
When your results are ready, your Dante Labs account will have a link to download the VCF file(s) directly onto your computer or mobile device (about 150-200 MB of space). You can also ask us to send your BAM and FASTQ files via a hard drive if you wish (about 200-250 GB).
We suggest using the Eve App by our partner Sequencing.com, directly on the Sequencing.com website. There, you’ll find a free or a paid version of the app (still less than $10!). Some third-party software tools were developed for microarray data and therefore, are not the best at interpreting VCF files generated from the next generation sequencing technologies we use. However, the Sequencing.com Eve App works very well with VCF files, so we highly recommend it!
We would suggest using the gVCF app by our partner Sequencing.com. You can access the app on the Sequencing.com website, costing you less than $20.
Your data is stored in our secure Amazon Web Services (AWS) cloud in the United States and Europe.
Whole Genome analyzes all the genes in your DNA.
Whole GenomZ and Whole GenomeM analyze all of your genes and the space between them. This means, every letter in your DNA is sequenced!
The 23andMe raw data file includes the letters (AA, CT, etc.) for about 650,000 SNPs, regardless of whether you have actually have differing genetic variants (from the reference genome) or not.
On the contrary, the VCF file, based on your entire DNA (all your SNPs!), whittles down the SNP data to provide you with the SNP variants that specifically differ from the reference genome.
Therefore, if you cannot find some SNPs, in your VCF file compared to your 23andMe file, it means that you do not have variants in those SNPs. This means that your SNPs ‘match’ the reference genome (meaning you’re healthy!) and the VCF has removed them so have immediate access to the SNPs where do differ.
Our mission is to make genetics accessible to everyone. Price has been a barrier for many people to access their genetic data for too long. Using an Amazon approach, we identified inefficiencies in typical genetic laboratory workflows. We found that most of the costs were not in the DNA sequencing process, but in the management of the samples before the sequencing, including DNA extraction, or in the bioinformatics processing after the sequencing. We have eliminated these inefficiencies and leveraged economies of scale to finally pass the cost savings to you.
Yes, we are fully compliant with the GDPR.
No. At Dante Labs, we work with saliva samples. This is because saliva is a non-invasive and effective way to collect your own DNA.
Dante Labs is built on trust. We respect your privacy and protect it with strong encryption and strict policies that govern how all of the data is handled. We are compliant with the GDPR and the UK Cyber Essentials, required by the National Health Service. We also have a sophisticated cloud structure to protect your data.
Furthermore, after you send us your saliva sample, your data, samples, results and reports are only identifiable by the barcode on the saliva collection tube.
Lastly, your reports and results include no personal identification information, meaning if lost you will remain anonymous.
The customized report is an additional option that we provide (free of charge) to patients who have a strong, justified interest for a specific condition or disease (ex. Epilepsy, Ehler Danlos, Periodic Paralysis, etc.).
This report has proven very useful, especially for patients with Rare Diseases.
For example, if you choose “Periodic Paralysis”, then we will generate a Periodic Paralysis virtual panel, containing all the variants associated with Periodic Paralysis. On top of this, we will generate a report with variants from other diseases, but which have similar symptoms called the ‘Secondary Report’.
The Secondary Report includes variants and genes of diseases with similar symptoms to your chosen disease of interest. We have experienced that with complex diseases, up to 20% of patients have been misdiagnosed with the wrong disease. Therefore, this Secondary Report has proven to be a very useful tool for both patients and doctors to achieve a precise diagnosis, and prevent the ‘diagnostic odyssey’ experienced by rare disease patients.
The NIH Genetics Home Reference is a great resource for fundamental topics related to human genetics: