Genomic

Sequence a complete genome (human, plant, animal, bacterial…) with ultra-long reads. Accurately resolve structural variants and repeat regions, and characterise base modifications (e.g. methylation), and haplotype phasing, with nanopore long reads.

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

Ask for

01/

Advantages

  • No DNA manipulation
  • Generation of ultra-long reads
  • Resolve complex genetic variants

02/

What can you get

  • Accurately detect structural variants at a nucleotide level resolution of the breakpoints
  • Detect variants undetected by other techniques (retrotransposon insertions, inversions, intronic structural variants)
  • Study haplotypes with phasing long-reads generated
  • Study repeat regions
  • Explore epigenetics on native DNA sample

Process of service


01
Sample preparation

DNA high quality 2ug

02
Fill the form

You can find the form on our website

03
Send your samples

When they arrive, our laboratory will take care of the rest.

04
Ready!

Download the results and analyze them

Process of service

01

Sample preparation

DNA high quality 2ug

02

Fill the form

You can find the form on our website

03

Send your samples

When they arrive, our laboratory will take care of the rest.

04

Ready!

Download the results and analyze them

FAQs

Here you will find answers to the most common questions we receive about our services. We are here to help you and make sure you have all the information you need.

More info

What type of sample do I need?
How long does the service take?
What type of service is right for my study?
What reading length is obtained?
What reading depth is obtained in targeted region (PCR)?
What reading depth is obtained in targeted region (enrichment)?