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Genomics facility - Long-read and short read DNA sequencing

Good to know

In short
  • Combines long- and short-read sequencing.
  • Needs high-quality DNA samples.
  • Fits complex genome projects.

Wageningen Genomics Facility provides accurate, scalable DNA sequencing for complex genomes and metagenomes, supporting high-quality data for advanced breeding.

What can you do at this facility?

What can you do here?

Using PacBio and Aviti, this facility offers a complete sequencing infrastructure for both long‑read and short‑read applications. Partners can perform de novo genome assemblies, structural variation analysis, full‑length transcriptome sequencing, population resequencing and metagenomics.  

Expert support is available for sample preparation, library construction and bioinformatics analysis. With high accuracy, scalability and extensive multiplexing options, projects of any size can be executed efficiently.

Who is this facility for?

Who for?

This facility is intended for researchers, breeding companies, biotech organisations and partners working on genomics, variability analysis, transcriptomics, metagenomics and biotechnology innovation.

“The combination of PacBio and Aviti enables researchers to execute every genomics project in the most effective way – from complex genome assemblies to population‑wide studies.”
Elio Schijlen
Researcher genomics

Why choose this facility?

Why this facility?

We offer:

  • Highly accurate HiFi reads with <0.1% error rate
  • Long-read sequencing without amplification bias
  • Up to 100 Gb output per flow cell
  • Possibilities for multiplexing
  • Ideal for complex genome and full length transcriptome analysis
Genomics Facility
Advanced sequencing for faster, smarter research.

Questions about this facility?

Contact

Get in touch with us for availability, pricing and application support.

dr. EGWM (Elio) Schijlen

Researcher genomics