mRNA-seq Service

mRNA-seq is the method of choice to efficiently detect and precisely quantify coding RNAs present in a biological sample under specific circumstances. Accurate estimation of transcript abundance allows for differential expression analysis as well as the study of alternative splicing and discovery of new transcript isoforms.

Our Epigenomics Profiling Services assure a fully integrated service-workflow for generation of mRNA-seq libraries, multiplexed sequencing and data analysis. Serviced library preparation is based on specific poly A selection to produce Illumina compatible libraries enriched in mRNAs.

High performance mRNA-seq

• Superior complexity and high transcript coverage
• Accurate comparison of gene expression levels
• Detection of novel transcripts, alternative splicing and gene fusion events
• Suitable for a broad range of input amounts
• Compatible with FFPE samples
• Fast turnaround time (from 5 to 6 weeks)