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Whole GenomeL - Long Reads Whole Genome Sequencing

Whole GenomeL - based on Third-generation sequencing (also known as long-read sequencing). The first Long Reads Whole Genome Sequencing available commercially, worldwide. Leveraging Third-generation sequencing technology in the Dante Labs Oxford Nanopore-certified lab

If you seek to get a Customized Report on a disease or gene panel, after receiving your saliva collection kit, fill out the form

Regular price €899.00 EUR Sale price

Compare at €1,299.00 EUR

What you get

Long Read Raw Data

Download your FASTQ, BAM and VCF files, with no extra charge.

CNV and SV

Leverage long reads for Copy Number Variations and Structural Variations

Customized Report

Customized Report on a disease or condition of your choice (ex. Epilepsy, Ehler Danlos)

Long reads Whole Genome Sequencing:

  • - Read length: average N50>20,000bp (vs. 150bp of short reads)
  • - Optimized for analysis of repeated sequences, copy number variations and structural variations
  • - Third generation sequencing
  • - First time available, global coverage
  • - Performed at Dante Labs own Oxford Nanopore-certified sequencing center

How it works

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Purchase Your Kit Online

Your kit will arrive in 2-3 Business days.

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Collect and Register

Follow the kit instructions to spit in the tube - all from home. Register your kit on our website and then mail the saliva sample tube back to us.

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Learn your results online

In about 8-10 weeks, we will send you an email to let you know that your results are ready.