Neuromics Support Facility offers a wide range of scientific support to researchers, scientists, industrial and commercial collaborators. Our focus is DNA, amplicon, plasmid and RNA sequencing, complemented with bioinformatics support. Team originates from within VIB-UAntwerp Center for Molecular Neurology (CMN), where we gathered theoretical and practical expertise in high throughput genetic analyses. Since 2002, we have been offering Sanger sequencing services to internal and external customers.Data processing is performed automatically and in optimal conditions. We also offer consultation and assistance upon customer’s request. Years of collaboration with industrial partners resulted in a setting and a methodology where confidentiality of the data is assured.

Contact us to discover how we can help you move from an idea to data within your budget.

As auxiliary services we also offer wide variety of DNA and RNA control, from UV-VIS, Fragment analysis and Fluorescence concentration measurements to full DNA and RNA QC, consisting of estimation of purity (UV/VIS), concentration (fluorescent analysis) and integrity (capillary analysis) (r). For QC requests please first contact us with a request via email and fill in Sequencing Order Form.

Sanger Sequencing service

NSF Sanger sequencing service utilizes automatized procedures, using Biomek® FX and NX liquid handlers for template preparation followed by sequencing reaction and sequencing loading on Applied Biosystems 3730XL DNA Analyzer, known as the gold standard for high throughput genetic analyses.

Sequencers are used for base detection and DNA fragment analysis applications. This instrument in combination with the very sensitive ABI PRISM® BigDye™ Terminator cycle sequencing kits yields long reads with low-level background, while multiple automation steps decrease costly human errors. For template cleanup, we use Illustra™ ExoProStar™ and for dye-terminator removal, Agencourt CleanSEQ beads.

Sanger details → How to order →

For Sanger sequencing service and support, please contact us on


Next to the Sanger sequencing, we offer on request several other non-standard services, such as DNA and RNA quality assessments. Since 2013, we provide low to high throughput (depending on the project) next-generation-sequencing services on Illumina platforms (MiSeq and NextSeq500). Our team focuses on targeted, exome and 3'UTR sequencing, but other applications are possible.

Next to sequencing, we offer data analysis and interpretation. Main strength of our analysis support lies in providing solutions using customized, comprehensive evaluation of genomic and transcriptomic data and includes current, advanced gene set and pathway modeling and annotations.

Costs of our services are project based and possible to receive upon project description. If you decide to submit your NGS project to us, please inquire and we will supply you with all needed information, including order and sample submission forms.

In 2017, our NGS fleet expanded by offering different applications using long read sequencing (ONT, Oxford Nanopore Technologies). Using our expertise and excellent collaboration between CMN scientists and VIB Innovation lab we have developed several strategies for library prep, sequencing and data analysis using direct, long read DNA, primarily for structural variants, single nucleotide variants and epigenetic analysis.

We also support targeted and cDNA sequencing, next to other applications, so do contact us, if native, long read sequencing can boost your research and science!

For NGS related projects and support, please contact us on and for bioinformatics support please contact us on

If you plan to include sequencing services in grant application or research strategy, feel free to contact us for assistance.

Our experts 

Mojca Strazisar

Head of NSF
Expert Scientist

Samuël Sluijs

Operational Technologist

Tim De Pooter

Expert Technologist

Geert Joris

Senior Technician