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FAQ Genome Sequencing

Transcriptome Analysis Services

Sequencing of cDNA or SAGE clones by Sanger technology with read lengths up to 1100 base pairs.

Ultra-deep sequencing of cDNA-, SAGE-, miRNA- and sncRNA-libraries with the Genome Sequencer™ FLX.

Specifications

Sequencing of EST or SAGE Clones by Sanger Technology

  • Clones can be delivered as stab or glycerol cultures in plates
  • Delivery of cDNA libraries as ligation- or transformation mix possible
  • High throughput DNA preparation and purification
  • High throughput sequencing with Sanger technology
  • Read length up to 1100 bases
  • Sequencing from the 5’-, the 3’- or both ends
  • Professional clustering and assembly
  • Additional bioinformatic services on request
  • High quality sequence data
  • Clones for further experiments available.

Sequencing of cDNA Libraries by GS FLX

  • Ultra Deep Sequencing of libraries
  • No cloning required, therefore no cloning bias
  • Sequencing from the 5’-, the 3’-end or shotgun sequencing is possible
  • No arrays necessary for expression studies
  • Detection of transcripts that are not on commercially available arrays.
Your Advantages
  • Ligation and transformation service included
  • Experience of over 100 large EST projects
  • cDNA library service available: “From tissue to the transcriptome”
  • No array necessary for expression studies.