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Whole genome sequencing. Depending on the genome of interest, in order to achieve the necessary coverage, you can choose MinION device (low size genome) or PromethION device (human genome).

What can I get with this technology?

  • Accurately detect structural variants at a nucleotide level resolution of the breakpoints.
  • Identify and characterise disease-specific variants in clinical samples, with rapid access to results.
  • Study haplotype phasing with genomic long-reads generated.
  • Identified complex variants not detected by previous routine molecular tests.

What do I have to do?
  1. Prepare your simple: DNA high quality 2ug (fill the formulary at the website)
  2. Send your samples to our lab
    1. Library preparation
    2. Nanopore sequencing + data analysis
    3. Report to the client
  3. Get Access and analyze your results

Time: 1 month aprox

Estimated prize: from 1.000-2.500€ depending on experiment design

Results obtained by this technology

Average coverage de 20X

Average read length: 4kb

Advantages
  • No DNA manipulation
  • Ultra long reads
  • Procesed and handle data provided