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Transcriptome sequencing is a powerful tool for quantifying transcripts and discovering novel transcripts and gene fusions.
We can sequence strand-specific mRNA libraries as well as total RNA library with or without depletion of ribosomal RNA using the following kits:

  • TruSeq® Stranded mRNA Sample Prep Kit
  • TruSeq® Stranded Total RNA - (with Ribo-ZeroTM Gold)
We offer a complete RNA-seq data analysis to study:
  • gene expression profile
  • new transcripts and isoforms
  • alternative splicing sites
  • fusion genes / structural variants
  • point mutations
We recommend 50 million reads for gene expression projects and 25 million reads for fusion genes identification.
For further information please fill out the form or write to