Custom RNA sequencing
Next-Gen sequencing can generate a lot of data that might not be useful for every project. To focus on the specific transcripts that matters for a given project, it is possible to create libraries only after 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.
• List of targets
• Proof of samples quality or integrity (Bioanalyzer traces or eq.)
Further details on the project may be requested directly by the expert. You will be able to exchange directly with the experts after filling in the form below.
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