Service

In recent years, Next Generation Sequencing (NGS) has fundamentally changed molecular genetic research. The Sequencing Facility of the Institute of Human Genetics at the Klinikum rechts der Isar primarily serves patient care and meets the highest quality standards. The facility operates state-of-the-art NGS and also offers NGS services for research projects on human samples.

Our team supports you in planning your projects. We take over the processing and sequencing of your samples and also offer bioinformatic analyses for data evaluation by arrangement. All procedures are carried out with diagnostic quality on an Illumina NovaSeq 6000. The samples are processed in our accredited laboratory. In addition, the Institute has a PromethION for long-read sequencing for research activities.

The generated sequence data is subjected to quality control at the Institute of Human Genetics and made available in the standard .fastq format. If desired, further bioinformatic analysis can also be carried out by the Institute of Human Genetics.

Our portfolio includes the following protocols:

- Whole genome sequencing (short and long read sequencing)

- Whole Exome Sequencing (Twist-Enrichment)

- RNA sequencing (short and long read sequencing of mRNA)

For all projects, please contact us in advance.

Contact us

Dr. Elisabeth Graf

elisabeth.graf2@mri.tum.de

and

Dr. Matias Wagner

matias.wagner@mri.tum.de

 

PD Dr. Michael Zech

michael.zech@mri.tum.de