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$229 Whole Genome Offer for DNA Day 2019, with 90-day result guarantee

$229 Whole Genome Offer for DNA Day 2019, with 90-day result guarantee

“The Dante Labs Whole Genome is making an important difference in the lives of rare disease patients. The reports and the data at the very least reveal part of the puzzle and often enable specialists to then focus on those findings and target efforts to treat the individual.” At Dante...

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Generoso Ianniciello

Our Response to the British Parliament Inquiry on Commercial Genomics

Our Response to the British Parliament Inquiry on Commercial Genomics

"We believe in freedom and knowledge. The DNA belongs to the individual. People have the right to learn about their DNA and have the right to choose."  The Science and Technology Committee of the British Parliament launched an inquiry into commercial genetic testing. We firmly believe in the freedom of choice....

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Andrea Riposati

Genetic Data: FASTQ, BAM and VCF

Genetic Data: FASTQ, BAM and VCF

With Dante Labs whole genomes, you always get your raw data. We give raw data because it represents your DNA, is yours, and is an asset for life: in the next months and years you will be able to use your raw data on new tools, by Dante Labs and...

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Generoso Ianniciello

Understanding the 30X of your Whole Genome Sequencing

Understanding the 30X of your Whole Genome Sequencing

Republishing from Sequencing.com What is 30X Whole Genome Sequencing What is 30x Whole Genome Sequencing? If you are interested in whole genome sequencing (WGS), read on to learn about the value of 30x coverage. In our last article, we discussed our partner Dante Labs and their clinical-grade 30x whole genome sequencing (WGS) test. In...

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Generoso Ianniciello

Long Reads Human Whole Genome Sequencing for Everyone

Long Reads Human Whole Genome Sequencing for Everyone

Dante Labs announced today the launch of the first commercial long reads whole genome sequencing, with 30x coverage, powered by Oxford Nanopore Promethion technology. The new test, named WholeGenomeL, will allow individuals to sequence their entire genome with long reads technology. The read length has averaged N50>20,000bp. Long reads sequencing is optimized for...

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Generoso Ianniciello

How Dante Labs Can Help You Get Your Diagnosis

How Dante Labs Can Help You Get Your Diagnosis

dante labs, mtDNA, rare disease day, rare disease month, rare disease odyssey, wgs, whole genome sequencing

It takes on average 7.6 years for a Rare Disease patient to receive a diagnosis.  If you’ve seen our Facts posted daily on Twitter and Facebook, then you’ll know this period of time is called the, ‘Rare Disease Odyssey’. During this length of time patients go undiagnosed or misdiagnosed, and...

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Andrea Riposati

Seven years of searching can turn into months using your own genetics

mitochondrial DNA, mtDNA, new york, rare disease day, rare disease month, rare disease odyssey, wgs, whole genome sequencing

Are you able to cast your mind back to seven and a half years ago?  For much of our 7 billion-strong population the memory that arises will be of little significance, but for the millions of rare disease patients out there, this memory is has led and changed the course...

User blog

Andrea Riposati