We are offering a broad range of different sequencing applications and help and guide our users to find the most efficient and econimic sequencing technology to answer their scientific questions. Our services cover routine NGS-based workflows as well as customized sequencing solutions.
We are applying different long read DNA and RNA sequencing, haplotyping, and scaffolding technologies to create de novo genome assemblies, improve upon existing assemblies, resolve highly-repetitive regions and annotate repeat and gene regions.
Many short-read applications involving Illumina sequencing are routinely performed by our colleagues in the DcGC. You are always welcome to get in touch with us and we will connect you with our experts.
Our DNA extraction portfolio ranges from rapid protocols for fast genotyping applications to the extraction of ultra-long and contaminant-free genomic DNA that is required for high-quality de novo genome assemblies. We have experience with different input including bacteria, plants, small animals, cultured cell, and extracted tissues of different species over multiple taxa.
We have also different electrophoresis systems in place that allow the separation of long and ultra-long gDNA fragments.
We are happy to discuss and help to find the best and most economical way of DNA extraction depending on your sample type and input amount always taking your follow up application into account.
We provide a service that designs and executes pipelines to characterize molecular events in genome engineering projects and a standard genotyping service of genetic model organisms.