NEW!
Up to 400MB assembled or mapped data
in five working days

RapidRun on Roche GS FLX

Full run with up to 400 MB

Up to one million reads with up to 400 bp

Including de novo assembly or mapping against one genome

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Tagging, Enrichment & Next Generation Sequencing

Deep sequencing of specific regions of a large number of samples

Enrichment strategies can be used for the analysis of genomes and transcriptomes. Tagging of samples allows for the combination of any number of samples with any size of targeted region to be sequenced. Therefore sample tagging/ barcoding decreases sequencing costs.  ...more

Next Generation sequencing

With the 454, Illumina and the Sanger technologies at our disposal we can always offer you the solution which is best for your individual project!

We are the only sequencing company in Europe working with the Roche GS FLX and Illumina Genome Analyzer II. We have several years of experience which enables us to objectively assess these Next Generation sequencing technologies and their intelligent combination for efficient hybrid strategies. Using an additional fleet of seven ABI 3730xl we realize your sequencing projects flexibly, cost-consciously and quickly; from genome and metagenome projects (de novo or re-sequencing) to transcriptome analyses (cDNA, SAGE) through to regulome studies (ChIP, microRNA)  ... more

Barcode sequencing

Convenient and safe sequencing with GATC barcodes! The handy barcode labels are available for single reads in tubes or plates - made-to-measure for your individual budget.

Simple ordering, one bill per order and unlimited validity! With the smart GATC barcode management system you can use your barcodes jointly with your colleagues and always keep track of things! ...more