RNA

Long, full-length reads by nanopore sequencing allows characterisation and quantification of full-length transcript isoforms of RNA or cDNA without fragmentation or amplification.

Ask for

01/

Advantages

  • No fragmentation of RNA, full length transcripts may be able to detect new isoforms. Reduce bias with PCR-free protocol

02/

What can you get

  • Characterization of full-length transcripts, splice variants and gene fusions 
  • Detection of new isoforms.
  • Detect base modifications using direct RNA (epitranscriptomics)
  • Identification of anti-sense transcripts and lncRNA isoforms

Process of service


01
Sample preparation

mRNA 500ng

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

mRNA 500ng

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)?