Whole genome sequencing (WGS)

Discover the full range of genetic variation

Whole genome sequencing (WGS) is a powerful method that provides high-resolution genetic information of model organisms and humans. We offer both resequencing and de-novo sequencing of genomes.

  • Resequencing is particularly useful to identify and compare genetic variations across closely related genomes.
  • De-novo sequencing allows to study the genetic information of newly discovered organisms, in-depth variant characterisation, and comparison of highly variable genomes.

Study mutations

Our bioinformatics tools facilitate precise identification of single nucleotide polymorphisms (SNPs), insertions/deletions (InDels), and copy number variants (CNVs). We provide variant analysis including high-quality mapping of short and long read data and summarizing SNPs, InDels, and CNVs in your sample. Reports will be provided in Variant Call Format (VCF).