Next-generation DNA sequencing makes it possible to rapidly compare the genetic content among samples and identify germline and somatic variants of interest, such as single nucleotide polymorphisms (SNPs), insertions and deletions (indels), copy number variants (CNVs), and other structural variations. We support a broad range of applications:


-- Exome-sequencing

-- Nimblegen MedExome

-- Custom targeted DNA sequencing

-- Whole genome sequencing


We support (targeted) DNA sequencing projects by providing project consultancy to guide you in study design, sample preparation and quality control. We apply standard QC and Quality Assesment of sequence data, and offer optional more advanced data analysis services, such as mapping reads and variant calling.



For more information, please contact dr. Gaby van Dijk.