Eurofins MWG Operon offers genome sequencing services by latest technology standards and fastest turnaround times.

We have unparalleled experience in fulfilling sequencing requirements since 1996. With us you find a service provider, which offers you complete solutions.

De-Novo and Comparative Sequencing of Bacterial and Fungal Genomes
Coverage sequencing or complete sequencing of unknown bacterial or fungal genomes or sequencing of metagenomes 

BAC, PAC, Cosmid, Fosmid Sequencing Services
High-throughput end sequencing of clones from both sides by state-of-the-art Sanger technology on ABI 3730XL sequencers, e.g. for the creation of physical maps. Coverage sequencing of defined BAC clones by Genome Sequencer™ FLX or ABI 3730 XL technology and closing of gaps by primer walking

Transcriptome Analysis Services
Sequencing of cDNA or SAGE clones by Sanger technology with read lengths up to 1100 base pairs. Ultra deep sequencing of standard, normalised, substracted and 3'-fragmented cDNA-, SAGE-, miRNA- and sncRNA-libraries with the Genome Sequencer™ FLX

Re-Sequencing of Exons and Genome Fragments 
Sequencing of exons in order to find a correlation between sequence deviations, for instance SNPs or deletions or different phenotypes

Ultra Deep Sequencing of Exons and Genome Fragments 
New method for a wide range of applications, including the detection of rare mutations or the study of methylation patterns with the Genome Sequencer™ FLX

Library Generation Service
Preparing of BAC libraries, arraying libraries into plates and spotting BAC clones onto nylon filters. Cosmid and Fosmid library service. Broad range of standard, normalised and subtracted cDNA libraries for transcriptome analysis. Preparing of samples (genomes, BACs, PACs or Cosmids etc.) for shotgun sequencing or other studies

Bioinformatic Service
Eurofins MWG Operon has the expertise, software and hardware to solve any of your bioinformatic requirements.