Custom RNA sequencing

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Service description

  • Next-Gen sequencing can generate a lot of data that might not be useful for every project.
  • To focus on the specific transcripts that matter for a given project, it is possible to create libraries only after the enrichment or amplification of a set of transcripts.
  • This is particularly useful in the case of difficult samples (such as paraffin-embedded tissue) or with low input of RNA (10 ng of total RNA), if the set of focus transcripts is identified.

Materials to provide

  • Samples.
  • List of targets.
  • Proof of samples quality or integrity (Bioanalyzer traces or eq.).

  • Further details on the project may be requested.
  • You will be able to exchange directly with the experts after filling in the form below.

Typical deliverables

  • Extraction.
  • Library preparation.
  • Depletion.
  • Sequencing of the samples with number of reads.
  • Paired-end reads.
  • Download link or a hard drive with raw data and the post-experiment analysis.
  • Study following the specifications validated with the Expert.
Capture d’écran 2020-10-16 à 10.57.43

Get started with your RNA sequencing project

Please answer the fields below to be contacted by our team of scientists

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