![[Translate to German:] Probenvorbereitung für Next-Generation-Sequencing](/fileadmin/images/headimages/hero_laborleistungen.jpg)
Whole Genome Sequencing (WGS). Complete analysis of the entire genome, both coding and non-coding regions, to identify alterations and mutations. WGS provides a comprehensive overview of an organism's genetic make-up and is used in various fields such as disease research, diagnostics and evolutionary research.
Whole Exome Sequencing (WES), also for clinical questions - focussed sequencing of protein-coding regions. WES is used to identify variations in coding regions, which can contribute to the diagnosis of genetic disorders, the understanding of disease mechanisms and potentially to personalised treatment strategies.
Do you have specific clinical questions? We offer you the Whole Exome Service with kits from IDT and Twist.
Panel sequencing of predefined sets of genes in connection with a clinical question or research objective is based on the HGMD, OMIM and ClinVar databases and provides significantly higher coverage and reliability compared to classic whole genome or whole exome sequencing
Targeted and genome-wide DNA methylation analyses for epigenetic studies
Sequencing of ready-to-use libraries for rapid conversion of already prepared samples
With this NGS platform, ATLAS Biolabs offers comprehensive support along the entire process chain - from library preparation and sequencing to optional bioinformatic analysis. Benefit from high data quality, short processing times and personalised advice.
