Sequencing Services and Tumor Analysis
Our vision is to make next-generation sequencing available to all life scientists and to bring diagnostic knowledge into sequencing service. We employ state-of-the-art sequencing technology. This, combined with our outstanding customer care and our know-how gained in clinical diagnostics, enables us to stand out from competitors. Every project at CeGaT is supervised by a dedicated project manager from start to completion. We are flexible and can accommodate to the requirements of our clients.
What you get:
- Processing according to diagnostic standards
- Project management by skilled experts
- Made in Germany
All of our services can be tailored to your requirements such as isolation of nucleic acids, data output format or further bioinformatic analyses.
Sequencing Service
Genome Sequencing
Get the most comprehensive collection of an individual’s genetic information
Exome Sequencing
Fast and precise, suited for your research
Transcriptome Sequencing
Analysis of all RNA molecules of a biological sample
Panel Sequencing
Examine a distinct set of regions within the genome
Ready to Load Sequencing
Flexible sequencing options, including different flow cells and read modes
Single-cell RNA Sequencing
Explore cellular diversity at single-cell level
Small RNA Sequencing
Discover small RNA molecules in your biological sample
Methylation Sequencing
Explore the Epigenome – Methylation Matters
Microbiome Analysis
16S Sequencing
Highly Accurate detection of Bacteria and Archaea
Shotgun Metagenomic Sequencing
Accurate detection of all microbes
Translational Oncology
Tumor Mutational Burden
Measurement of the biomarker TMB
Liquid Biopsy
Isolation and analysis of cell-free DNA in the blood
Immunology
HLA Typing
Reliable and accurate insights into HLA types
T-Cell Receptor Sequencing
Investigate diversity, clonality and changes in the T-cell repertoire or single TCR clones
Data Ownership
CeGaT guarantees that the data generated within the research project remain the exclusive property of the customer. Samples, sequencing data, and analysis results are only used for the purposes specified in the project agreement. We carry out all project steps in-house to ensure no third parties have access to any data. No data nor sample material will be sold to others.
What our customers say about us
Contact Us
Start Your Project Now
We are happy to discuss sequencing options and to find a solution specifically tailored to your clinical study or research project.
When getting in contact, please specify sample information including starting material, number of samples, preferred library prep option, preferred sequencing depth and required bioinformatics, if possible.
