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Whole GenomeL - Long Reads Whole Genome Sequencing for Researchers

  • The first commercial Long Reads (third generation sequencing) Whole Genome Sequencing Test
  • Suggested for large structural variations (CNVs, SVs, large INDELs)
  • Performed in the Dante Labs Oxford Nanopore-certified lab
  • Results in only 8-12 weeks
  • Whole Genome Sequencing 30X

Suggested for healthcare professionals and researchers interested in exploring the large structural variations of human DNA.

Regular price €799.00 EUR Sale price

€1,299.00 EUR

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What you get

  • - 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

Raw Data available (FASTQ, BAM and VCF files).

Discover the new Health Manager: the easiest way to access your Genome.
To access the Sample Account, use sample@dantelabs.com and insert dantelabs in the password field

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.