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Whole Genome Sequencing for Rare Diseases

Whole Genome Sequencing for Rare Diseases

The whole genome sequencing is the new approach in genetics for rare diseases. More and more rare disease patients and their specialists are leveraging the investigative power of the whole genome to develop a better diagnosis, identify the most effective treatment and prevent side effects from adverse drug reaction before they happen. Old...

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Adam Risser

Dante Labs CEO Andrea Riposati speech from 2019 London Calling

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Andrea Riposati

New Tool to Manage Your Kits

Dear Dante Labs community, We have deployed a new Tool to manage your Kits. This tool has new functions, including new levels of protection for your privacy and security. IMPORTANT: you will have to reset your password the first time you use it (you can use the same password as...

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Adam Risser

Introducing Dante Labs Business: A B2B Portal for Advanced Genetics Dedicated to Healthcare Professionals and Researchers

Introducing Dante Labs Business: A B2B Portal for Advanced Genetics Dedicated to Healthcare Professionals and Researchers

London, May 28, 2019 (Newswire.com) - Dante Labs today announced the launch of Dante Labs Business for Healthcare Professionals and Researchers (http://b2b.dantelabs.com), a new portal that combines the advanced analytics, access to newest technologies and genetics expertise that thousands of individuals have come to know and love from Dante Labs, with new...

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Riccardo Paone

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