This site use cookies for access statistics purposes. Click here for details about cookies policy. Closing this banner you accept the use of these cookies. Close and accept cookies





RNA SEQ

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 info@galseq.com.